Oxidative Medicine and Cellular Longevity

Oxidative Medicine and Cellular Longevity / 2019 / Article

Review Article | Open Access

Volume 2019 |Article ID 4727283 | https://doi.org/10.1155/2019/4727283

Yinuo Guan, Xianjing Song, Wei Sun, Yiran Wang, Bin Liu, "Effect of Hypoxia-Induced MicroRNA-210 Expression on Cardiovascular Disease and the Underlying Mechanism", Oxidative Medicine and Cellular Longevity, vol. 2019, Article ID 4727283, 12 pages, 2019. https://doi.org/10.1155/2019/4727283

Effect of Hypoxia-Induced MicroRNA-210 Expression on Cardiovascular Disease and the Underlying Mechanism

Academic Editor: Ji C. Bihl
Received03 Feb 2019
Revised08 Apr 2019
Accepted06 May 2019
Published21 May 2019


Cardiovascular diseases have high morbidity and mortality rates worldwide, and their treatment and prevention are challenging. MicroRNAs are a series of noncoding RNAs with highly conserved sequences and regulate gene expression by inhibiting mRNA transcription or degrading targeting proteins. MicroRNA-210 is significantly upregulated during hypoxia and plays a protective role by inhibiting apoptosis and regulating cell proliferation, differentiation, migration, mitochondrial metabolism, and angiogenesis in hypoxic cells. MicroRNA-210 expression is altered in cardiovascular diseases such as atherosclerosis, acute myocardial infarction, preeclampsia, aortic stenosis, and heart failure, and overexpression of microRNA-210 in some of these diseases exerts protective effects on target organs. Furthermore, chronically upregulated miR-210 potentially plays a marked pathogenic role in specific situations. This review primarily focuses on the upstream pathways, downstream targets, clinical progress in cardiovascular disease, and potential applications of microRNA-210.

1. Introduction

Cardiovascular diseases (CVDs) currently have the highest morbidity and mortality rates worldwide, in both developing and developed countries, and the number of lives lost increases every year [1]. According to recent statistics from the American Heart Association on heart disease and stroke, 17.3 million people die every year from CVD-related complications globally [2]. In addition to continuous research on the prevention and treatment of CVD, the development of strategies for improving the quality of life and prognosis of patients with CVD has recently emerged as an important avenue of study.

MicroRNAs (miRNAs) are small molecules of 20–26 nucleotides with a highly conserved sequence of single chain-encoded RNA [3]. Accumulating evidence indicates that miRNAs regulate many biological processes such as cell proliferation, differentiation, apoptosis, autophagy, mitochondrial metabolism, angiogenesis, tumor formation, and hematopoiesis [4, 5]. These regulatory effects are largely achieved by destabilizing target mRNAs or inhibiting translation [6]. To date, more than 700 species of miRNAs that regulate 20–30% of all protein-coding genes in the human body have been identified [3]. Among these, microRNA-210 (miR-210) is a well-known hypoxia miRNA, which leads to similar changes in most cell lines [7]. miR-210 is upregulated in normal cells exposed to hypoxia and in hypoxic tumor cells and has shown great therapeutic potential in various diseases [811]. Studies have established the role of miR-210 in almost all hypoxia-related phenomena, such as angiogenesis, apoptosis, differentiation, proliferation, cell cycle regulation, mitochondrial metabolism, DNA damage repair, and tumor growth [12].

Although numerous genes are regulated by miR-210, only a few have a protective function against CVD [1316]. Most of the products of these genes mediate the protective response of the cardiovascular system to hypoxia and improve the adaptability of cells and individuals to hypoxia through various biological functions. Furthermore, miR-210 potentially enhances the progression of some chronic diseases, such as pulmonary arterial hypertension (PAH) [17]. Here, we review the most recent studies on miR-210 and its expression patterns in relation to CVD. Based on the identified target genes of miR-210 and associated pathways and functions, we highlight the prospects of miR-210 as a target for future treatment and prevention of CVD.

2. miR-210 and Its Activators

The most common and prominent cause of CVD is hypoxia, which leads to irreversible tissue damage [18]. Kulshreshtha et al. and Camps et al. first reported that miR-210, located in the intronic sequence AK123483 mRNA, is hypoxia-inducible [11, 19]. Many subsequent studies have since confirmed that miR-210 expression can be induced by hypoxia, which is triggered by the expression of hypoxia-inducible factor-alpha (HIF-α) including HIF-1α and HIF-2α [8, 2022]. The HIF molecule is prolyl-hydroxylated by three homologous 2-oxoglutarate-dependent dioxygenases PHD1, PHD2, and PHD3 and ubiquitinated and rapidly degraded by the von Hippel-Lindau (VHL) protein under normal conditions [23, 24]. HIF-1α accumulates in most cell lines owing to inhibition of PHD during hypoxia conditions, followed by translocation to the nucleus, wherein it interacts with aromatic hydrocarbon nuclear transfer protein (ARNT) [25, 26]. HIF-1α binds to the miR-210 promoter at approximately 40 bp upstream of the transcription initiation site and upregulates miR-210. Consistently, Kulshreshtha et al. confirmed that anti-HIF-1α antibody immunoprecipitated the miR-210 promoter fragments in hypoxic cells, albeit to a minor extent in normoxic controls [11]. Furthermore, miR-210 was reportedly downregulated in HIF-1α knockout mice, compared with the wild-type mice [27]. Wang et al. [28] analyzed infarcted heart tissues from patients who died of acute myocardial infarction (AMI), reporting that miR-210 was significantly upregulated in the infarcted samples compared with those of the control group (accidental death). Interestingly, HIF-1α was downregulated in the AMI samples, suggesting that miR-210 may function as an HIF1-α inhibitor.

Although previous studies reported that the regulation of hypoxia-response element (HRE) with miR-210 displays specificity towards HIF-1α rather than HIF-2α [20], some studies reported that miR-210 may be upregulated via an HIF-1α-independent pathway recently. Zhang et al. [29] used RNA interference to silence HIF-2α in 786-O-pBABE cells, which are predominantly HIF-2α-dependent for HIF activity, and reported significant silencing of miR-210. Similarly, Kulshreshtha et al. [11] investigated the effect of exogenous constitutively active HIF-2α in several tumor cells and reported that miR-210 is upregulated. The HIF-2α pathway depends on dimerization with ARNT, and a deletion of ARNT results in complete inactivation of the HIF pathway.

However, miR-210 was also upregulated in the absence of a complete HIF signal conduction in fibroblasts of aromatic ARNT-knockout mouse embryos, indicating that miR-210 is regulated by other pathways in addition to HIF-1α or HIF-2α [10]. p53, which also directly binds to the miR-210 promoter, is a well-known posttranslational regulator of protein degradation in response to stress, including hypoxia. It regulates important cellular activities, such as the cell cycle and apoptosis, and also suppresses inflammation in various human tissues [30]. p53 reportedly plays a role in miRNA processing through interaction with Dicer and is an important component for pre-miRNA processing to fully active miRNA [31]. Regulation by p53 suggests that miR-210 also plays a protective role in inflammation or other stimulations besides hypoxia. In addition to the p53 pathway, the AKT pathway plays an important role in regulating miR-210. Kim et al. [32] reported that the AKT and ERK1/2 pathways promote miR-210 through an HIF-1α-independent pathway. Shi et al. [33] reported that insulin can stimulate miR-210 expression via the PI3K/AKT pathway. Stimulation of AKT expression potentially upregulates miR-210 [10]. Furthermore, NF-κB also induces miR-210 expression under hypoxia. Subunit p50 of NF-κB, a protein related to inflammation and DNA repairing, localizes at a 200 bp core promoter region immediately upstream of the miR-210 stem-loop. Sequence analysis of NF-κB p50 binding with miR-210 was also reported by Zhang et al. [34]. Moreover, serum response factor (SRF), as an exogenous miRNA promotor, can regulate several miRNAs, including miR-210. Chromatin immunoprecipitation (ChIP) revealed a direct interaction between SRF and miR-210, which inhibited the proliferation and differentiation of cardiac progenitor cells in embryonic stem cell-derived embryoids [35].

3. Clinical Relevance of miR-210 in CVD

Similar to HIF-1α, p53, AKT, and NF-κB serve as protective components in various diseases in the cardiovascular system [10, 28, 33, 36]. Studies using animal models of CVD have indicated a protective role of miR-210. In AMI rats, miR-210 upregulation and adenomatous polyposis coli (APC) downregulation can be observed in cardiomyocytes (CM), suggesting that APC potentially participates in the reduction of cell death and promotion of angiogenesis via miR-210 regulation [21]. Li et al. [15] established a mouse model of atherosclerosis through administration of a high-fat diet, wherein miR-210 was significantly upregulated and the proapoptotic protein, 3-phosphoinositide-dependent protein kinase-1 (PDK1), was inhibited. Moreover, the significant upregulation of vascular endothelial growth factor (VEGF) and hepatocyte growth factor (HGF) in miR-210 overexpressing mice clearly suggests an increased angiogenic potential of miR-210 [3739]. In CVD, miR-210 is believed to protect the cardiovascular system from potentially lethal damage by inhibiting cell apoptosis and promoting angiogenesis, thus potentially leading to revascularization.

Although no clinical study has reported the precise association between miR-210 and cardiovascular protection, alterations in miR-210 expression are often observed in peripheral blood or damaged tissues from patients with CVD, including atherosclerosis, acute coronary syndrome, valvular heart disease, pulmonary arterial hypertension, and heart failure. Moreover, changes in miR-210 expression have been reported in some cardiovascular-associated diseases, such as preeclampsia and diabetes. These changes are associated with typical genes or proteins involved in cardiovascular damage or repair (Table 1). Hale et al. [40] confirmed Argonaute 2 as a major regulator of specific circulating miRNAs under dynamic conditions, released together with circulating miR-210 under hypoxic conditions. Argonaute 2 potentially facilitates miR-210 delivery to recipient cells and protects individuals exposed to hypoxia. Thus, a consensus regarding the potential applications of miR-210 to evaluate disease severity and predict disease prognosis has been established (Figure 1).

TargetFunctionCell lineReferences

APCAntiproliferation, proapoptosis, and cell cycle inhibitionCM, HCtASMC, and HCAEC[21, 41]
CtgfAntiangiogenesis, profibrosisHL-1, cardiac fibroblast[43, 44]
Dapk1Cell cycle inhibition, proapoptosis, and antimigrationHL-1[43]
E2F3Cell cycle inhibition, proapoptosishPASMC, CM[45, 46]
EFNA3Antiangiogenesis, proapoptosisCT, HL-1, and HUVEC[34, 43, 47]
HGFProangiogenesis, proproliferation, promigration, and prodifferentiationHUVEC[39]
ISCUMitochondrial metabolism progressionH9C2, hPASMC, and hPAEC[7, 14, 17, 48]
Ptp1bAntiangiogenesis, proapoptosisHL-1[43]
ROD1Antidifferentiation (seedless)HUVEC[50]
RUNX3Antiproliferation, antimigrationHUVEC[51]
SPRED2AntimigrationHASMC, HUVEC[52]
VEGFProangiogenesis, promigration, and proinvasionHUVEC[21, 37, 38, 47, 51]

3.1. Atherosclerosis

Atherosclerosis is characterized by chronic inflammation, which not only is limited to the heart but also involves peripheral vessels, causing stenosis in the femoral arteries and carotid arteries. Raitoharju et al. [53] analyzed samples obtained from carotid and femoral endarterectomy or in coronary artery bypass grafting with a PCR array and reported that the level of miR-210 was increased significantly and that one of its downstream target genes, potassium channel modulatory factor 1 (KCMF1), was significantly downregulated. Another study reported that miR-210 levels were significantly increased in blood samples from patients with arteriosclerosis obliterans compared to those of controls [54]. Thus, both of these studies suggest miR-210 as a biomarker for atherosclerosis. Eken et al. [41] reported that circulating miR-210 levels were lower in patients with unstable fiber caps compared to those with stable atherosclerotic plaques. This study not only indicates that miR-210 potentially plays a role in stabilizing atherosclerotic plaques but also suggests its feasibility as a marker for the risk of rupture of atherosclerotic plaques. Zhang et al. [55] identified six miRNAs, including miR-210, which were elevated in patients with ischemic heart disease. After comparing the Gensini score of each of the coronary heart disease (CHD) patients with the miRNA levels, they found that miR-210 expression was negatively correlated with the Gensini score, suggesting its potential utility as a marker for the severity of CHD.

3.2. Acute Coronary Syndrome

Acute coronary syndrome (ACS) is a more urgent and high-risk CVD than atherosclerosis, which can cause acute ischemia and severe damage through blockade of blood flow in cardiovascular tissue [56]. In an animal model of AMI, Hu et al. [43] injected a plasmid containing miR-210 into the experimental group. Postinjection, the left ventricular (LV) function of the experimental group was significantly healthier than that of the control group. They further reported an increase in angiogenesis and a reduction in the apoptotic rate and infarct size in the group injected with miR-210. Arif et al. [21] presented the same conclusion using mice of different germ lines. Fan et al. [39] proved the protective effect of miR-210 in AMI mice through histological evaluation and changes in cardiac function. Simultaneously, they reported upregulation of CD31, a typical protein involved in angiogenesis. Collectively, these findings confirmed that miR-210 has a significant protective effect on the cardiovascular system in AMI.

In a clinical study, Karakas et al. [57] followed up 1112 patients with coronary artery disease, including 430 patients with ACS and 682 patients with stable angina pectoris, who underwent coronary angiography for four years after surgery. They measured eight different miRNAs in the plasma, which were found to be associated with cardiovascular events, to evaluate the prognostic value of circulating miRNAs, showing that miR-210 expression is associated with cardiovascular-related death by approximately three standard deviations in ACS. This is the largest study conducted to date to evaluate the prognostic value of circulating miRNAs in coronary artery disease (CAD), providing significant and valuable clinical guidance. These studies reported the potential of miRNAs as biomarkers for risk estimation in CAD. Another study reported an increase of seven miRNAs, including miR-210, in the blood samples of AMI patients compared with healthy controls. In addition, the expression of HIF1-α/miR-210 as a group of hypoxia-marker genes in myocardial tissue was significantly associated with AMI-associated mortality [28].

3.3. Valvular Heart Disease

miR-210 is reportedly associated with valvular heart disease. Rosjo et al. [58] reported an increase in circulating miR-210 in patients with aortic stenosis compared with age- and sex-matched controls, and the NT-proBNP level showed the same increasing trend. The authors suggested that the increase of miR-210 may be derived from epithelial cells or the myocardium. During the subsequent 1287 d of follow-up, 26% (15) of the patients died, and a significant association was reported between higher circulating levels of miR-210 and increased mortality. This study suggests that miR-210 is a candidate index of risk and prognosis for aortic stenosis patients.

3.4. Pulmonary Arterial Hypertension

PAH is a potentially lethal and highly prevalent vascular disease characterized by increased pulmonary arterial pressure and lung vasculopathy [59]. A well-known cause of PAH is hypoxia and the activity of HIF-1α and HIF-2α [60]. Gou et al. [45] generated a PAH mouse model via chronic hypoxia, reported significant miR-210 upregulation, and showed that miR-210 upregulation plays an antiapoptotic role in hPASMCs. However, the responses of the pulmonary vascular tissue to hypoxia and HIF factors in PAH are partially associated with chronic repression of mitochondrial metabolism. ISCU1/ISCU2 plays an important role in PAH pathogenesis as a key component of mitochondrial metabolism, which could be regulated by miR-210 [17]. miR-210 is reportedly increased significantly in the small diseased pulmonary arterioles in human PAH lung tissues compared with arterioles observed in nondiseased human lung tissue. Circulating extracellular miR-210 is elevated in plasma samples adjacent to the pulmonary vascular space compared with samples from PAH-free individuals [17]. This study initially reports the progressive role of miR-210 to PAH through the inhibition of the ISCU1/2-FeS pathway through disease induction with SU5416. In turn, chronic miR-210 expression led to elevated right ventricular systolic pressure (RVSP) and induced pulmonary vascular remodeling [17]. Interestingly, SU5416, which can specifically induce PAH, induces the expression of miR-210 in whole lung tissue and in small pulmonary vessels, with no effects on miR-210 in the heart and other organs. In addition, levels of other reported miR-210 targets including E2F transcription factor 3 (E2F3) and Ephrin-A3 (EFNA3) remained unchanged, indicating an important role of ISCU1/2 in the specific activity of miR-210 in PAH. Therefore, the function of miR-210 in PAH is controversial.

3.5. Heart Failure

Because of the irreversible nature of myocardial injury, many CVDs eventually develop into heart failure. A plasma PCR array for patients with chronic heart failure revealed miR-210 upregulation [61]. Semenza reported that the mature miR-210 contents in mononuclear cells from blood samples of patients with congestive heart failure are associated with the existing diagnostic criteria for N-terminal probrain natriuretic peptide (NT-proBNP), which is recommended as a diagnostic tool for heart failure by the American Heart Association in 2005 and 2009 [26]. Moreover, although there was no significant correlation between miR-210 and NT-proBNP in NYHA-level 2 plasma, the miR-210 level was relatively lower in patients with improved NT-proBNP [62], indicating that miR-210 not only can be considered a marker for detecting the severity of heart failure but also could predict the prognosis of patients with heart failure.

3.6. Preeclampsia

Although there is no clear evidence of an association of miR-210 with primary or secondary hypertension, numerous studies have reported a significant increase in miR-210 in the blood of patients with preeclampsia (PE) [34, 6366]. The disease manifests as high blood pressure during pregnancy, probably owing to hypoxia caused by insufficient placental perfusion. One method of generating a PE model is injecting the TLR3 promoter in pregnant mice, which can increase blood levels of miR-210, which is regulated by both HIF1-α-dependent and HIF1-α-independent pathways [67]. Biro et al. [63] collected blood samples from patients with chronic hypertension, gestational hypertension, and mild or severe PE, along with a normal control group and a normal pregnancy group. Although they found a significant difference in the relative exosomal hsa-miR-210-3p expression levels between all disease subgroups compared to the normotensive group, only the PE subgroups showed a significant upregulation in miR-210. Using a PCR array to analyze the miRNA expression levels in PE patients, Murphy et al. [66] reported no apparent reduction in the levels of miR-210 and other related miRNAs after one year, suggesting that women with PE during pregnancy had persistent inflammation after childbirth. In addition to the blood, miR-210 upregulation was also detected in the placental tissue of PE patients. In addition, miR-210 reportedly regulates glucose metabolism and iron deposition in Swan 71 trophoblasts and BeWo choriocarcinoma cell lines through inhibition of ISCU [68]. A relationship between miR-210 expression and fetal weight was demonstrated in this clinical trial. Zhang et al. [34] reported that upregulated miR-210 expression in PE-related cells was involved in the regulation of EFNA3 and/or HOXA9 and other genes. In addition, the authors analyzed the expression of miR-210 in five different types of placentas and assessed mitochondrial function, showing that oxidative stress and reactive oxygen species (ROS) were produced in the placenta tissue cells of PE patients, thus increasing miR-210 levels and inhibiting mitochondrial-related ISCU, which potentially contributes to mitochondrial dysfunction [69]. These results were confirmed using the same cell line in vitro.

Hydroxysteroid 17β-dehydrogenase type 1 (HSD17B1), a steroid-producing enzyme that is primarily expressed in the placenta, is also one of the proteins regulated by miR-210. The mRNA and protein expression levels of HSD17B1 were significantly reduced in the placentas of PE patients with a concomitant reduction in plasma HSD17B1 protein levels. In addition, a prospective cohort study reported significantly reduced plasma HSD17B1 levels in pregnant women between 20–23 and 27–30 weeks before the onset of PE in comparison with subjects with a normal pregnancy. The authors concluded that expression of HSD17B1 in the placenta of PE patients is under the control of miR-210 and that plasma HSD17B1 levels are decreased before the onset of PE, suggesting HSD17B1 as a potential prognostic marker for PE [70].

3.7. Diabetes

Patients with diabetes often develop cardiac diseases [71, 72]. miR-210 is reportedly specifically upregulated in diabetes patients undergoing tests for heart failure. Although the levels of most of the detected miRNAs did not significantly differ between nondiabetes and diabetes patients with heart failure, the miR-210 level in the diabetes group was significantly higher [73]. Moreover, diabetes itself can cause changes in miR-210 expression in the body. Costantino et al. [74] reported several upregulated miRNAs, including miR-210, in a mouse model of streptozotocin-induced diabetes. miR-210 overexpression was further reported in Zucker diabetic fatty rats [75]. In clinical studies, elevated miR-210 has been detected in both the plasma and urine of adolescent type I diabetes mellitus patients, suggesting that high sugar itself can cause oxidative stress in cells [76]. Amr et al. [77] evaluated miR-210 expression in type 2 diabetes with or without CAD and reported that it is upregulated in both groups of diabetic patients. However, between these two groups, patients with CAD had a more significant miRNA change than those with diabetes alone.

4. The Protective Mechanism of miR-210 In Vitro CVD Models

As a prognostic miRNA in CVD, miR-210 regulates the number of genes and proteins related to cardiac models. Plasmids coding miR-210 injected into the myocardium of an AMI mouse model improved cardiac function, reduced infarct size, prevented endogenous myocardial apoptosis, and induced angiogenesis, suggesting that miR-210 potentially reduces cell death by regulating apoptosis in adult mice and promoting angiogenesis [21]. Further, Lu et al. [48] reported that HIF/miR-210/ISCU serves as an important signaling axis regulating mitochondrial metabolism, protecting rats from chronic hypoxia-induced PAH. These results indicate that miR-210 protects cells from stimulations through various mechanisms (Table 2).


AntiapoptosisAPC/BNIP3/CASP8AP2/Dapk1/E2F3/EFNA3/PDK1/Ptp1b[15, 16, 21, 34, 4143, 45, 46]
ProangiogenesisCtgf/HGF/Ptp1b/VEGF[3739, 43, 47, 51]
ProproliferationAPC/HGF/ HOXA9/MKP1/RUNX3[21, 34, 39, 41, 49, 51]
PromigrationDapk1/HGF/KCMF1/RUNX3/SPRED2/VEGF[21, 3739, 43, 47, 5153]
ProdifferentiationHGF/ROD1[39, 50]
Cell cycle progressionAPC/Dapk1/E2F3/EFNA3[21, 34, 39, 41, 43, 4547]
AntifibrosisCtgf[43, 44]
Mitochondrial metabolism inhibitionISCU[7, 14, 48]

4.1. Antiapoptosis

One of the primary protective effects of miR-210 is to inhibit apoptosis and promote cell survival. Li et al. [42] reported that miR-210 reduces apoptosis through inhibiting the caspase-8 pathway in H2O2-stimulated human umbilical vein endothelial cells (HUVECs). Similarly, Diao et al. [16] reported that miR-210 specifically inhibits the expression of the proapoptotic gene BNIP3 (BCL2/adenovirus E1B 19 kDa protein-interacting protein 3), thereby preventing apoptosis in H9C2 cells. Li et al. [15] used oxidized low-density lipoprotein (ox-LDL) to induce miR-210 in human aortic endothelial cells (HAECs), demonstrating a negative correlation with PDK1 levels. Inhibition of miR-210 expression reportedly significantly reduced apoptosis in HAECs, whereas PDK1 overexpression reportedly reversed the proapoptotic effect of miR-210 through the P13K/AKT/mTOR pathway.

Several genes promote apoptosis through regulation of the cell cycle. APC is a part of the canonical Wnt signaling pathway that negatively regulates cell cycle progression by promoting β-catenin degradation, which could lead to cell death [21]. Highly expressed miR-210 in human carotid artery smooth muscle cells (HCtASMC) and human carotid artery endothelial cells (HCAEC) in a hypoxic condition can inhibit APC expression and consequently reduce apoptosis [41]. Another target of miR-210 is E2F3, a potential target for functional involvement in apoptosis, as its deletion leads to inhibition of apoptosis [13]. Under oxygen-glucose deprivation/reperfusion, upregulated miR-210 protects cardiomyocytes by inhibiting E2F3 [46]. Moreover, Hu et al. [43] reported that hypoxia upregulates miR-210 in HL-1 cells and inhibits EFNA3 and death-associated protein kinase 1 (Dapk1) to enhance the adaptation of HL-1 cells to hypoxia. These two genes reportedly play a negative role in the cell cycle and are related to apoptosis.

4.2. Proangiogenesis

When CVD affects the function of the cardiovascular system, an important mechanism of reducing injury is through angiogenesis. Angiogenesis is the process of formation of new blood vessels from preexisting vessels, which plays a role in cardiomyocyte growth, survival, and contractile function [78]. This involves several phenomena, including cell proliferation, differentiation, migration, and regulation of angiogenic factors. APC is involved in cell proliferation regulated by miR-210 according to Arif et al. [21]. Similar to APC, miR-210 also targets E2F3, which is closely related to cell proliferation [79]. Significant upregulation of miR-210 and downregulation of E2F3 expression have been reported in a hypoxia model of human pulmonary artery smooth muscle cells (hPASMCs), and expression of E2F3 was induced when miR-210 was inhibited [45]. The expression of MAP kinase phosphatase 1 (MKP1) in hPASMCs is also regulated by miR-210, and targeted inhibition of miR-210 reduces the proliferation of hPASMCs. Moreover, overexpression of miR-210 prevents hypoxia-induced MKP1 expression with no effects on cell proliferation. Inhibition of MKP1 by small interfering RNA abolished the miR-210-dependent prevention of cell proliferation under hypoxia [49]. Furthermore, in placental cytotrophoblast cells (CTs), Zhang et al. [34] detected the expression of cell proliferation-related genes EFNA3 and homeobox A9 (HOXA9), which are regulated by miR-210. Hypoxia in CTs is a major cause of PE [80]. Interestingly, miR-210 downregulated the EFNA3 protein but not the mRNA in HUVECs [47]. Further, runt-related transcription factor 3 (RUNX3) was also identified as the direct target of miR-210 in HUVECs [51]. Overexpression of miR-210 downregulated RUNX3 and promoted the proliferation and migration of HUVECs, while overexpression of RUNX3 inhibited these effects. Sprouty-related enabled/vasodilator-stimulated phosphoprotein homology 1 domain-containing protein 2 (SPRED2) inhibits cell migration by negatively regulating the mitogen-activated protein kinase pathway. Moreover, human aortic smooth muscle cells (HASMCs) and HUVECs can be protected from ox-LDL by producing excess miR-210 [52]. This effect was achieved by inhibiting SPRED2. Furthermore, connective tissue growth factor (Ctgf), which is downregulated by miR-210, plays an important role in angiogenesis and fibrosis [43, 44]. Studies have reported the upregulation of Ctgf in the infarct zone of AMI rats in both cardiac fibroblasts and cardiac myocytes [81]. Therefore, we suggest that downregulated Ctgf by miR-210 could promote angiogenesis and reduce myocardium fibrosis.

VEGF is a topical gene that regulates cell proliferation and migration. It was reportedly upregulated in HUVECs in response to hypoxia [37, 47, 51]. Overexpression of miR-210 significantly upregulated VEGF and promoted the proliferation, migration, and invasiveness of HUVECs [21, 38]. Protein tyrosine phosphatase 1B (Ptp1b) is a 50 kDa enzyme on the endoplasmic reticulum, which negatively regulates the VEGF pathway in endothelial cells (ECs) [82]. As a target of miR-210, downregulated Ptp1b promotes angiogenesis and reduces apoptosis [43]. Furthermore, Dapk1 is reportedly an miR-210 target that regulates cell migration. HGF, similar to VEGF, is also an angiogenesis-related protein, which has positive effects in HUVECs under hypoxia by regulating cell proliferation, migration, and differentiation [39].

In addition, Fasanaro et al. [50] identified regulator of differentiation 1 (ROD1) as a target of miR-210. ROD1 regulates cell differentiation, and its overexpression significantly inhibits cell proliferation. Although it does not have a distinct complementary sequence to that of miR-210, ROD1 is still regulated by miR-210. This indicates the existence of a class of proteins that are regulated by miRNAs without a seed sequence. This possibility has revealed novel avenues for future studies on miR-210.

4.3. Inhibition of Mitochondrial Metabolism

The shift in energy metabolism is another key to the survival of CMs under hypoxia or other stimulations. Iron is an essential metal necessary for normal cellular processes, including metabolism, heme synthesis, cell proliferation, and hypoxic response [17, 83]. The two major iron-containing molecules in the body are Fe/S clusters and heme, which are both involved in mitochondrial metabolism.

Iron-sulfur cluster scaffold protein (ISCU) is a key chaperone for the assembly of cellular ISCs and their transportation to enzymes, such as the mitochondrial respiratory complexes (complexes I, II, and III), which are responsible for mitochondrial respiration and energy production [14]. ISCU was first identified as a target gene of miR-210 in 2009 by Chan et al. in the human pulmonary arterial endothelial cells (HPAECs) [7]. Under hypoxic stress, miR-210 can target and downregulate ISCU in tumor cells, vascular endothelial cells, and many other cell types, thereby affecting the Krebs cycle, electron transport, ion metabolism, the production of ROS, and the function of mitochondria [84]. Sun et al. [14] reported that miR-210 regulates the shift in cellular energy metabolism during H2O2-induced oxidative stress in H9C2 CMs by targeting ISCU and indirectly regulating sirtuin 3 (SIRT3), which is also involved in energy metabolism. In hPASMCs, ISCU1/2 downregulation decreased Fe-S-dependent mitochondrial respiration and promoted a metabolic shift toward glycolysis for energy production. In a rat model of pulmonary hypertension, ISCU promoted the remodeling of pulmonary vessels by forming a positive feedback loop affecting the activity of mito-KATP and the proliferation of hPASMCs [48].

Further, miR-210 decrease heme levels by targeting ferrochelatase (FECH) in CMs, which is induced by HIF [85]. The final and rate-limiting step occurs in the mitochondria, where FECH inserts an iron molecule into protoporphyrin IX to generate heme. Qiao et al. [83] reported that overexpression of ISCU does not affect changes mediated by miR-210 in heme and FECH, showing that regulation of FECH by miR-210 is independent of ISCU. However, FECH levels increased without reversal via miR-210 knockdown during hypoxia, suggesting that the effects of miR-210 on heme are restricted to normoxic conditions and that the pathway is overridden during hypoxia. Therefore, further studies are required to determine the association between miR-210 and heme.

4.4. Inhibition of Inflammation

During hypoxia and other stimulations, immune responses eliminate damaged cells and tissues. However, excessive immune response can lead to inflammatory reactions and severe damage to heart tissue. Since miR-210 could be activated by NF-κB, miR-210 regulates inflammation by targeting several key genes in inflammatory pathways.

STAT6, an important member of the STAT family, is a key responder to the stimulation by interleukin-4 (IL-4) and IL-13 in the differentiation of T helper 2 cells [86]. Kopriva et al. [67] reported that TLR3-induced placental miR-210 downregulated the STAT6/interleukin-4 pathway, thus protecting PE mice from inflammatory injury.

In adult mice with acute ischemic brain injury, miR-210 inhibition significantly downregulated proinflammatory cytokines (TNF-α, IL-1β, and IL-6) and chemokines (CCL2 and CCL3) but had no significant effect on anti-inflammatory factors (TGF-β and IL-10) [87]. Moreover, antiphospholipid antibody- (aPL-) induced inflammation of trophoblast cells resulted in significant upregulation of miR-210 [88]. The TLR4 antagonist downregulated miR-210 in this model, thus showing the TLR4-dependent regulation of miR-210. These results revealed a close association between miR-210 and inflammation, providing potential issues related to CVD.

5. Therapeutic Potential of miR-210

Spinetti et al. [89] reported a trend of increasing miR-210 levels in the plasma of long-living individuals (LLIs; aged >90 years) compared to those of younger sex-matched controls. Interestingly, they reported miR-210 upregulation in the nonhealthy group of LLIs compared to healthy LLIs. This difference may be associated with the migration of miR-210-stimulated cells and may also be associated with the regulation of miR-210 during mitochondrial metabolism and ROS production. In this process, the two predicted target genes of miR-210, CXCR4 and BPIFB4, displayed a significant correlation with miR-210 expression. Thus, these two genes may provide a unique expression signature of health conservation with aging, independent of lifespan. Indeed, CXCR4 is considered a marker of healthy aging. Further studies involving pregnant women chronically living at high altitudes in comparison with those living at a sea level displayed an increase in the level of miR-210 expression [40], thus providing evidence regarding miR-210 as a hypoxia-protective miRNA in healthy individuals.

Recent animal experiments have identified certain drugs that can upregulate miR-210. Saffron has long been used in traditional medicine owing to its various pharmacological effects such as antioxidant, anticancer, anti-inflammatory, and antiatherosclerotic effects [90]. Crocin is an active ingredient in saffron, considered responsible for the beneficial effects. Ghorbanzadeh et al. [91] administered a single dose of crocin (50 mg/kg) and/or voluntary exercise for eight weeks in a rat model and reported an increase in miR-210, AKT, and ERK1/2 levels in the myocardial tissues compared to the control. Moreover, the crocin+exercise group displayed significant changes in various indicators. Together, these results suggest that saffron and exercise can be combined as a new potential therapeutic or preventive strategy to overcome certain CVDs.

Another study reported that pretreatment of a mouse model of AMI with Huoxue Anxin Recipe (HAR) upregulated miR-210 expression, while the untreated group displayed a relative downregulation of miR-210 [38]. Moreover, the ejection fraction, fractional shortening of the mice, in the HAR treatment group was higher than that in the AMI-untreated group, and the infarct size was smaller than that in the untreated group. Furthermore, the upregulation of vascular endothelial growth factor suggested that these effects might be achieved by promoting myocardium angiogenesis. Olmesartan is a member of angiotensin II receptor blockers, which plays an important role in treating hypertension [92]. When evaluating the protective function of olmesartan in a rat model of spontaneously hypertensive myocardial ischemia reperfusion, Lu et al. [93] reported that miR-210 is a relatively independent indicator of myocardial protection.

Owing to the unique nature of the heart tissue, the damage caused by CVD is usually irreversible. Although current therapeutic interventions for CHD can improve clinical outcomes and prolong lifespans, they are essentially palliative in nature because they fail to address the underlying issues of the loss of CMs. Recent studies have attempted to regenerate heart tissue by inducing the differentiation of various stem cells. Early stem cell transplantation is directly related to the recovery of late cardiac function [94]. However, the low survival rate of stem cells after transplantation has been a major obstacle to their clinical application [95]. Intermittent hypoxia can protect cells via the HIF1-α pathway [96], and miR-210 can affect cell migration, differentiation, and angiogenesis and inhibit apoptosis. Accordingly, Kim et al. [95] performed two rounds of 30 min hypoxic preconditioning on bone marrow-derived mesenchymal stem cells (MSCs), which were then injected into the myocardium of an AMI model. miR-210 was significantly upregulated in the group with preconditioned MSCs, and the cell viability was improved after implantation in the rats. These effects may have been achieved by inhibiting the apoptotic protein caspase-8. In another experiment, miR-210 expression was induced in MSCs, which promoted the survival of CMs in coculture, and miR-210 was induced and transferred by exosomes in both cell types [97]. In the same cell line, Wen et al. [98] stimulated miR-210 via sevoflurane preconditioning, thus exerting the same effect as that of transplanted stem cells. Ma et al. [99] reported that endothelial progenitor cells can protect endothelial cells through exosome-derived miR-210, which promotes this protective effect by improving mitochondrial function. In a study on human endothelial stem cells (hESCs), Kane et al. [100] reported elevated miR-210 during differentiation of hESCs into functional vascular endothelial cells, suggesting that miRNA-210 can promote angiogenesis. Xu et al. [101] conducted a detailed study on the protective mechanism of miR-210 overexpression in MSCs, showing that it improved the survival of MSCs under oxidative stress through antioxidation and the activation of the c-Met pathway. These results provide a rationale for stem cell-based therapy. The same prosurvival effect was also reported in myocardial progenitor cells (MPCs), displaying less CM apoptosis, enhanced angiogenesis, and improved LV ejection in the miR-210-injected group in comparison with hearts injected with cell culture medium [102]. A plasmid harboring HIF1-α and CPCs were simultaneously implanted into the injured myocardium of rats. The infarct size was relatively small, and the ejection fraction of the rats was higher after AMI compared to the control group. These findings indicate that the implanted HIF1-α can prolong the survival of transplanted CPCs, preventing cardiac remodeling, reducing the infarct size, and promoting angiogenesis. Furthermore, this function is at least partially mediated by miR-210 [103]. Finally, Emanueli et al. [104] reported elevated plasma miR-210 levels in patients undergoing coronary artery bypass grafting, which was primarily focused on the exosomes, confirming that miR-210 is transferred via exosomes in the repair of myocardial injury.

6. Conclusion

Emerging evidence suggests that miR-210 can be considered an independent indicator of the extent of cellular damage and for severity assessment of various clinical CVDs. In addition, miR-210 can also predict the prognosis of diseases such as atherosclerosis and PE and can guide the development of follow-up treatment strategies. miR-210 is also expected to play a protective role in heart tissue, especially during stem cell transplantation and heart transplantation. Although negative functions have been reported in some situations associated with CVDs, miR-210 upregulation is clearly associated with protection of cardiovascular cells.

In conclusion, miRNA-210, as a recognized hypoxic miRNA, offers great potential in treating CVDs. Thus, further studies are required to investigate the cardiovascular protective mechanism of miR-210 and its future application.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


  1. GBD 2017 Causes of Death Collaborators, “Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980-2017: a systematic analysis for the Global Burden of Disease Study 2017,” The Lancet, vol. 392, no. 10159, pp. 1736–1788, 2018. View at: Google Scholar
  2. E. J. Benjamin, S. S. Virani, C. W. Callaway et al., “Heart disease and stroke statistics—2018 update: a report from the American Heart Association,” Circulation, vol. 137, no. 12, pp. e67–e492, 2018. View at: Publisher Site | Google Scholar
  3. B. Kusenda, M. Mraz, J. Mayer, and S. Pospisilova, “MicroRNA biogenesis, functionality and cancer relevance,” Biomedical Papers, vol. 150, no. 2, pp. 205–215, 2006. View at: Publisher Site | Google Scholar
  4. A. Bavelloni, G. Ramazzotti, A. Poli et al., “MiRNA-210: a current overview,” Anticancer Research, vol. 37, no. 12, pp. 6511–6521, 2017. View at: Publisher Site | Google Scholar
  5. C. X. Ren, R. X. Leng, Y. G. Fan, H. F. Pan, C. H. Wu, and D. Q. Ye, “MicroRNA-210 and its theranostic potential,” Expert Opinion on Therapeutic Targets, vol. 20, no. 11, pp. 1325–1338, 2016. View at: Publisher Site | Google Scholar
  6. B. Ason, D. K. Darnell, B. Wittbrodt et al., “Differences in vertebrate microRNA expression,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 39, pp. 14385–14389, 2006. View at: Publisher Site | Google Scholar
  7. S. Y. Chan, Y. Y. Zhang, C. Hemann, C. E. Mahoney, J. L. Zweier, and J. Loscalzo, “MicroRNA-210 controls mitochondrial metabolism during hypoxia by repressing the iron-sulfur cluster assembly proteins ISCU1/2,” Cell Metabolism, vol. 10, no. 4, pp. 273–284, 2009. View at: Publisher Site | Google Scholar
  8. L. Cicchillitti, V. di Stefano, E. Isaia et al., “Hypoxia-inducible factor 1-α induces miR-210 in normoxic differentiating myoblasts,” The Journal of Biological Chemistry, vol. 287, no. 53, pp. 44761–44771, 2012. View at: Publisher Site | Google Scholar
  9. H. Wang, S. Bian, and C. S. Yang, “Green tea polyphenol EGCG suppresses lung cancer cell growth through upregulating miR-210 expression caused by stabilizing HIF-1α,” Carcinogenesis, vol. 32, no. 12, pp. 1881–1889, 2011. View at: Publisher Site | Google Scholar
  10. R. K. Mutharasan, V. Nagpal, Y. Ichikawa, and H. Ardehali, “MicroRNA-210 is upregulated in hypoxic cardiomyocytes through Akt- and p53-dependent pathways and exerts cytoprotective effects,” American Journal of Physiology-Heart and Circulatory Physiology, vol. 301, no. 4, pp. H1519–H1530, 2011. View at: Publisher Site | Google Scholar
  11. R. Kulshreshtha, M. Ferracin, S. E. Wojcik et al., “A microRNA signature of hypoxia,” Molecular and Cellular Biology, vol. 27, no. 5, pp. 1859–1867, 2007. View at: Publisher Site | Google Scholar
  12. X. Huang, Q. T. Le, and A. J. Giaccia, “MiR-210--micromanager of the hypoxia pathway,” Trends in Molecular Medicine, vol. 16, no. 5, pp. 230–237, 2010. View at: Publisher Site | Google Scholar
  13. L. A. Martinez, E. Goluszko, H. Z. Chen et al., “E2F3 is a mediator of DNA damage-induced apoptosis,” Molecular and Cellular Biology, vol. 30, no. 2, pp. 524–536, 2010. View at: Publisher Site | Google Scholar
  14. W. Sun, L. Zhao, X. Song et al., “MicroRNA-210 modulates the cellular energy metabolism shift during H2O2-induced oxidative stress by repressing ISCU in H9c2 cardiomyocytes,” Cellular Physiology and Biochemistry, vol. 43, no. 1, pp. 383–394, 2017. View at: Publisher Site | Google Scholar
  15. Y. Li, C. Yang, L. Zhang, and P. Yang, “MicroRNA-210 induces endothelial cell apoptosis by directly targeting PDK1 in the setting of atherosclerosis,” Cellular & Molecular Biology Letters, vol. 22, no. 1, 2017. View at: Publisher Site | Google Scholar
  16. H. Diao, B. Liu, Y. Shi et al., “MicroRNA-210 alleviates oxidative stress-associated cardiomyocyte apoptosis by regulating BNIP3,” Bioscience, Biotechnology, and Biochemistry, vol. 81, no. 9, pp. 1712–1720, 2017. View at: Publisher Site | Google Scholar
  17. K. White, Y. Lu, S. Annis et al., “Genetic and hypoxic alterations of the microRNA‐210‐ISCU1/2 axis promote iron–sulfur deficiency and pulmonary hypertension,” EMBO Molecular Medicine, vol. 7, no. 6, pp. 695–713, 2015. View at: Publisher Site | Google Scholar
  18. J. D. Maclay, D. A. McAllister, and W. Macnee, “Cardiovascular risk in chronic obstructive pulmonary disease,” Respirology, vol. 12, no. 5, pp. 634–641, 2007. View at: Publisher Site | Google Scholar
  19. C. Camps, F. M. Buffa, S. Colella et al., “hsa-miR-210 is induced by hypoxia and is an independent prognostic factor in breast cancer,” Clinical Cancer Research, vol. 14, no. 5, pp. 1340–1348, 2008. View at: Publisher Site | Google Scholar
  20. X. Huang, L. Ding, K. L. Bennewith et al., “Hypoxia-inducible mir-210 regulates normoxic gene expression involved in tumor initiation,” Molecular Cell, vol. 35, no. 6, pp. 856–867, 2009. View at: Publisher Site | Google Scholar
  21. M. Arif, R. Pandey, P. Alam et al., “MicroRNA-210-mediated proliferation, survival, and angiogenesis promote cardiac repair post myocardial infarction in rodents,” Journal of Molecular Medicine, vol. 95, no. 12, pp. 1369–1385, 2017. View at: Publisher Site | Google Scholar
  22. G. L. Semenza, “Hypoxia-inducible factor 1 and cardiovascular disease,” Annual Review of Physiology, vol. 76, no. 1, pp. 39–56, 2014. View at: Publisher Site | Google Scholar
  23. L. E. Huang, J. Gu, M. Schau, and H. F. Bunn, “Regulation of hypoxia-inducible factor 1α is mediated by an O2-dependent degradation domain via the ubiquitin-proteasome pathway,” Proceedings of the National Academy of Sciences of the United States of America, vol. 95, no. 14, pp. 7987–7992, 1998. View at: Publisher Site | Google Scholar
  24. P. C. Mahon, K. Hirota, and G. L. Semenza, “FIH-1: a novel protein that interacts with HIF-1α and VHL to mediate repression of HIF-1 transcriptional activity,” Genes & Development, vol. 15, no. 20, pp. 2675–2686, 2001. View at: Publisher Site | Google Scholar
  25. C. J. Schofield and P. J. Ratcliffe, “Oxygen sensing by HIF hydroxylases,” Nature Reviews Molecular Cell Biology, vol. 5, no. 5, pp. 343–354, 2004. View at: Publisher Site | Google Scholar
  26. G. L. Semenza, “Targeting HIF-1 for cancer therapy,” Nature Reviews Cancer, vol. 3, no. 10, pp. 721–732, 2003. View at: Publisher Site | Google Scholar
  27. A. Merlo, C. Bernardo-Castiñeira, I. Sáenz-de-Santa-María et al., “Role of VHL, HIF1A and SDH on the expression of miR-210: implications for tumoral pseudo-hypoxic fate,” Oncotarget, vol. 8, no. 4, pp. 6700–6717, 2017. View at: Publisher Site | Google Scholar
  28. Y. Wang, X. Pan, Y. Fan et al., “Dysregulated expression of microRNAs and mRNAs in myocardial infarction,” American Journal of Translational Research, vol. 7, no. 11, pp. 2291–2304, 2015. View at: Google Scholar
  29. Z. Zhang, H. Sun, H. Dai et al., “MicroRNA miR-210 modulates cellular response to hypoxia through the MYC antagonist MNT,” Cell Cycle, vol. 8, no. 17, pp. 2756–2768, 2009. View at: Publisher Site | Google Scholar
  30. N. Barabutis, A. V. Schally, and A. Siejka, “P53, GHRH, inflammation and cancer,” eBioMedicine, vol. 37, pp. 557–562, 2018. View at: Publisher Site | Google Scholar
  31. H. I. Suzuki, K. Yamagata, K. Sugimoto, T. Iwamoto, S. Kato, and K. Miyazono, “Modulation of microRNA processing by p53,” Nature, vol. 460, no. 7254, pp. 529–533, 2009. View at: Publisher Site | Google Scholar
  32. J. H. Kim, S. G. Park, S. Y. Song, J. K. Kim, and J. H. Sung, “Reactive oxygen species-responsive miR-210 regulates proliferation and migration of adipose-derived stem cells via PTPN2,” Cell Death & Disease, vol. 4, no. 4, article e588, 2013. View at: Publisher Site | Google Scholar
  33. Y. F. Shi, N. Liu, Y. X. Li et al., “Insulin protects H9c2 rat cardiomyoblast cells against hydrogen peroxide-induced injury through upregulation of microRNA-210,” Free Radical Research, vol. 49, no. 9, pp. 1147–1155, 2015. View at: Publisher Site | Google Scholar
  34. Y. Zhang, M. Fei, G. Xue et al., “Elevated levels of hypoxia-inducible microRNA-210 in pre-eclampsia: new insights into molecular mechanisms for the disease,” Journal of Cellular and Molecular Medicine, vol. 16, no. 2, pp. 249–259, 2012. View at: Publisher Site | Google Scholar
  35. G. Zheng, Y. Tao, W. Yu, and R. J. Schwartz, “Brief report: SRF–dependent miR–210 silences the sonic hedgehog signaling during cardiopoesis,” Stem Cells, vol. 31, no. 10, pp. 2279–2285, 2013. View at: Publisher Site | Google Scholar
  36. J. W. Gordon, J. A. Shaw, and L. A. Kirshenbaum, “Multiple facets of NF-κB in the heart: to be or not to NF-κB,” Circulation Research, vol. 108, no. 9, pp. 1122–1132, 2011. View at: Publisher Site | Google Scholar
  37. F. Liu, Y. L. Lou, J. Wu et al., “Upregulation of microRNA-210 regulates renal angiogenesis mediated by activation of VEGF signaling pathway under ischemia/perfusion injury in vivo and in vitro,” Kidney & Blood Pressure Research, vol. 35, no. 3, pp. 182–191, 2012. View at: Publisher Site | Google Scholar
  38. J. Wang, Y. Zhang, Y. M. Liu et al., “Huoxue Anxin Recipe () promotes myocardium angiogenesis of acute myocardial infarction rats by up-regulating miR-210 and vascular endothelial growth factor,” Chinese Journal of Integrative Medicine, vol. 22, no. 9, pp. 685–690, 2016. View at: Publisher Site | Google Scholar
  39. Z. G. Fan, X. L. Qu, P. Chu et al., “MicroRNA-210 promotes angiogenesis in acute myocardial infarction,” Molecular Medicine Reports, vol. 17, no. 4, pp. 5658–5665, 2018. View at: Publisher Site | Google Scholar
  40. A. Hale, C. Lee, S. Annis et al., “An Argonaute 2 switch regulates circulating miR-210 to coordinate hypoxic adaptation across cells,” Biochimica et Biophysica Acta (BBA) – Molecular Cell Research, vol. 1843, no. 11, pp. 2528–2542, 2014. View at: Publisher Site | Google Scholar
  41. S. M. Eken, H. Jin, E. Chernogubova et al., “MicroRNA-210 enhances fibrous cap stability in advanced atherosclerotic lesions,” Circulation Research, vol. 120, no. 4, pp. 633–644, 2017. View at: Publisher Site | Google Scholar
  42. T. Li, X. Song, J. Zhang et al., “Protection of human umbilical vein endothelial cells against oxidative stress by microRNA-210,” Oxidative Medicine and Cellular Longevity, vol. 2017, Article ID 3565613, 11 pages, 2017. View at: Publisher Site | Google Scholar
  43. S. Hu, M. Huang, Z. Li et al., “MicroRNA-210 as a novel therapy for treatment of ischemic heart disease,” Circulation, vol. 122, Supplement 1, no. 11, pp. S124–S131, 2010. View at: Publisher Site | Google Scholar
  44. M. M. Chen, A. Lam, J. A. Abraham, G. F. Schreiner, and A. H. Joly, “CTGF expression is induced by TGF- β in cardiac fibroblasts and cardiac myocytes: a potential role in heart fibrosis,” Journal of Molecular and Cellular Cardiology, vol. 32, no. 10, pp. 1805–1819, 2000. View at: Publisher Site | Google Scholar
  45. D. Gou, R. Ramchandran, X. Peng et al., “miR-210 has an antiapoptotic effect in pulmonary artery smooth muscle cells during hypoxia,” American Journal of Physiology-Lung Cellular and Molecular Physiology, vol. 303, no. 8, pp. L682–L691, 2012. View at: Publisher Site | Google Scholar
  46. W. S. Bian, P. X. Shi, X. F. Mi et al., “miR-210 protects cardiomyocytes from OGD/R injury by inhibiting E2F3,” European Review for Medical and Pharmacological Sciences, vol. 22, no. 3, pp. 743–749, 2018. View at: Publisher Site | Google Scholar
  47. P. Fasanaro, Y. D'Alessandra, V. di Stefano et al., “MicroRNA-210 modulates endothelial cell response to hypoxia and inhibits the receptor tyrosine kinase ligand Ephrin-A3,” Journal of Biological Chemistry, vol. 283, no. 23, pp. 15878–15883, 2008. View at: Publisher Site | Google Scholar
  48. Y. Lu, J. Huang, S. Geng et al., “MitoKATP regulating HIF/miR210/ISCU signaling axis and formation of a positive feedback loop in chronic hypoxia-induced PAH rat model,” Experimental and Therapeutic Medicine, vol. 13, no. 5, pp. 1697–1701, 2017. View at: Publisher Site | Google Scholar
  49. Y. Jin, T. Pang, L. D. Nelin et al., “MKP‐1 is a target of miR‐210 and mediate the negative regulation of miR‐210 inhibitor on hypoxic hPASMC proliferation,” Cell Biology International, vol. 39, no. 1, pp. 113–120, 2015. View at: Publisher Site | Google Scholar
  50. P. Fasanaro, S. Romani, C. Voellenkle, B. Maimone, M. C. Capogrossi, and F. Martelli, “ROD1 is a seedless target gene of hypoxia-induced miR-210,” PLoS One, vol. 7, no. 9, article e44651, 2012. View at: Publisher Site | Google Scholar
  51. Z. Zheng, L. Liu, Y. Zhan, S. Yu, and T. Kang, “Adipose-derived stem cell-derived microvesicle-released miR-210 promoted proliferation, migration and invasion of endothelial cells by regulating RUNX3,” Cell Cycle, vol. 17, no. 8, pp. 1026–1033, 2018. View at: Publisher Site | Google Scholar
  52. K. C. Chen, Y. C. Liao, J. Y. Wang, Y. C. Lin, C. H. Chen, and S. H. Juo, “Oxidized low-density lipoprotein is a common risk factor for cardiovascular diseases and gastroenterological cancers via epigenomical regulation of microRNA-210,” Oncotarget, vol. 6, no. 27, pp. 24105–24118, 2015. View at: Publisher Site | Google Scholar
  53. E. Raitoharju, L. P. Lyytikäinen, M. Levula et al., “miR-21, miR-210, miR-34a, and miR-146a/b are up-regulated in human atherosclerotic plaques in the Tampere Vascular Study,” Atherosclerosis, vol. 219, no. 1, pp. 211–217, 2011. View at: Publisher Site | Google Scholar
  54. T. Li, H. Cao, J. Zhuang et al., “Identification of miR-130a, miR-27b and miR-210 as serum biomarkers for atherosclerosis obliterans,” Clinica Chimica Acta, vol. 412, no. 1-2, pp. 66–70, 2011. View at: Publisher Site | Google Scholar
  55. H. Zhang, J. Hao, X. Sun, Y. Zhang, and Q. Wei, “Circulating pro-angiogenic micro-ribonucleic acid in patients with coronary heart disease,” Interactive Cardiovascular and Thoracic Surgery, vol. 27, no. 3, pp. 336–342, 2018. View at: Publisher Site | Google Scholar
  56. J. L. Looi, M. Lee, M. W. I. Webster, A. C. Y. To, and A. J. Kerr, “Postdischarge outcome after Takotsubo syndrome compared with patients post-ACS and those without prior CVD: ANZACS-QI 19,” Open Heart, vol. 5, no. 2, article e000918, 2018. View at: Publisher Site | Google Scholar
  57. M. Karakas, C. Schulte, S. Appelbaum et al., “Circulating microRNAs strongly predict cardiovascular death in patients with coronary artery diseaseresults from the large AtheroGene study,” European Heart Journal, vol. 38, no. 7, pp. 516–523, 2017. View at: Publisher Site | Google Scholar
  58. H. Røsjø, M. B. Dahl, A. Bye et al., “Prognostic value of circulating microRNA-210 levels in patients with moderate to severe aortic stenosis,” PLoS One, vol. 9, no. 3, article e91812, 2014. View at: Publisher Site | Google Scholar
  59. J. Bienertova-Vasku, J. Novak, and A. Vasku, “MicroRNAs in pulmonary arterial hypertension: pathogenesis, diagnosis and treatment,” Journal of the American Society of Hypertension, vol. 9, no. 3, pp. 221–234, 2015. View at: Publisher Site | Google Scholar
  60. S. Bonnet, E. D. Michelakis, C. J. Porter et al., “An abnormal mitochondrial–hypoxia inducible factor-1α–Kv channel pathway disrupts oxygen sensing and triggers pulmonary arterial hypertension in fawn hooded rats: similarities to human pulmonary arterial hypertension,” Circulation, vol. 113, no. 22, pp. 2630–2641, 2006. View at: Publisher Site | Google Scholar
  61. D. S. Zhao, Y. Chen, H. Jiang et al., “Serum miR-210 and miR-30a expressions tend to revert to fetal levels in Chinese adult patients with chronic heart failure,” Cardiovascular Pathology, vol. 22, no. 6, pp. 444–450, 2013. View at: Publisher Site | Google Scholar
  62. K. Endo, Y. Naito, X. Ji et al., “MicroRNA 210 as a biomarker for congestive heart failure,” Biological & Pharmaceutical Bulletin, vol. 36, no. 1, pp. 48–54, 2013. View at: Google Scholar
  63. O. Biró, B. Alasztics, A. Molvarec, J. Joó, B. Nagy, and J. Rigó Jr, “Various levels of circulating exosomal total-miRNA and miR-210 hypoxamiR in different forms of pregnancy hypertension,” Pregnancy Hypertension, vol. 10, pp. 207–212, 2017. View at: Publisher Site | Google Scholar
  64. K. R. Bounds, V. L. Chiasson, L. J. Pan, S. Gupta, and P. Chatterjee, “MicroRNAs: new players in the pathobiology of preeclampsia,” Frontiers in Cardiovascular Medicine, vol. 4, p. 60, 2017. View at: Publisher Site | Google Scholar
  65. D. S. Jairajpuri, Z. H. Malalla, N. Mahmood, and W. Y. Almawi, “Circulating microRNA expression as predictor of preeclampsia and its severity,” Gene, vol. 627, pp. 543–548, 2017. View at: Publisher Site | Google Scholar
  66. M. S.-Q. Murphy, R. C. Casselman, C. Tayade, and G. N. Smith, “Differential expression of plasma microRNA in preeclamptic patients at delivery and 1 year postpartum,” American Journal of Obstetrics and Gynecology, vol. 213, no. 3, pp. 367.e1–367.e9, 2015. View at: Publisher Site | Google Scholar
  67. S. E. Kopriva, V. L. Chiasson, B. M. Mitchell, and P. Chatterjee, “TLR3-induced placental miR-210 down-regulates the STAT6/interleukin-4 pathway,” PLoS One, vol. 8, no. 7, article e67760, 2013. View at: Publisher Site | Google Scholar
  68. D. C. Lee, R. Romero, J. S. Kim et al., “miR-210 targets iron-sulfur cluster scaffold homologue in human trophoblast cell lines: siderosis of interstitial trophoblasts as a novel pathology of preterm preeclampsia and small-for-gestational-age pregnancies,” The American Journal of Pathology, vol. 179, no. 2, pp. 590–602, 2011. View at: Publisher Site | Google Scholar
  69. S. Muralimanoharan, A. Maloyan, J. Mele, C. Guo, L. G. Myatt, and L. Myatt, “miR-210 modulates mitochondrial respiration in placenta with preeclampsia,” Placenta, vol. 33, no. 10, pp. 816–823, 2012. View at: Publisher Site | Google Scholar
  70. O. Ishibashi, A. Ohkuchi, M. M. Ali et al., “Hydroxysteroid (17-β) dehydrogenase 1 is dysregulated by miR-210 and miR-518c that are aberrantly expressed in preeclamptic placentas: a novel marker for predicting preeclampsia,” Hypertension, vol. 59, no. 2, pp. 265–273, 2012. View at: Publisher Site | Google Scholar
  71. A. Faria and S. J. Persaud, “Cardiac oxidative stress in diabetes: mechanisms and therapeutic potential,” Pharmacology & Therapeutics, vol. 172, pp. 50–62, 2017. View at: Publisher Site | Google Scholar
  72. R. Retnakaran and B. R. Shah, “Role of type 2 diabetes in determining retinal, renal, and cardiovascular outcomes in women with previous gestational diabetes mellitus,” Diabetes Care, vol. 40, no. 1, pp. 101–108, 2017. View at: Publisher Site | Google Scholar
  73. S. Greco, P. Fasanaro, S. Castelvecchio et al., “MicroRNA dysregulation in diabetic ischemic heart failure patients,” Diabetes, vol. 61, no. 6, pp. 1633–1641, 2012. View at: Publisher Site | Google Scholar
  74. S. Costantino, F. Paneni, T. F. Lüscher, and F. Cosentino, “MicroRNA profiling unveils hyperglycaemic memory in the diabetic heart,” European Heart Journal, vol. 37, no. 6, pp. 572–576, 2016. View at: Publisher Site | Google Scholar
  75. D. Delic, C. Eisele, R. Schmid, G. Luippold, E. Mayoux, and R. Grempler, “Characterization of micro-RNA changes during the progression of type 2 diabetes in Zucker diabetic fatty rats,” International Journal of Molecular Sciences, vol. 17, no. 5, p. 665, 2016. View at: Publisher Site | Google Scholar
  76. J. Osipova, D. C. Fischer, S. Dangwal et al., “Diabetes-associated microRNAs in pediatric patients with type 1 diabetes mellitus: a cross-sectional cohort study,” The Journal of Clinical Endocrinology and Metabolism, vol. 99, no. 9, pp. E1661–E1665, 2014. View at: Publisher Site | Google Scholar
  77. K. S. Amr, H. Abdelmawgoud, Z. Y. Ali, S. Shehata, and H. M. Raslan, “Potential value of circulating microRNA-126 and microRNA-210 as biomarkers for type 2 diabetes with coronary artery disease,” British Journal of Biomedical Science, vol. 75, no. 2, pp. 82–87, 2018. View at: Publisher Site | Google Scholar
  78. L. Badimon, R. Suades, G. Arderiu, E. Peña, G. Chiva-Blanch, and T. Padró, “Microvesicles in atherosclerosis and angiogenesis: from bench to bedside and reverse,” Frontiers in Cardiovascular Medicine, vol. 4, p. 77, 2017. View at: Publisher Site | Google Scholar
  79. A. Y. Olsson, A. Feber, S. Edwards et al., “Role of E2F3 expression in modulating cellular proliferation rate in human bladder and prostate cancer cells,” Oncogene, vol. 26, no. 7, pp. 1028–1037, 2007. View at: Publisher Site | Google Scholar
  80. R. Rampersad and D. M. Nelson, “Trophoblast biology, responses to hypoxia and placental dysfunction in preeclampsia,” Frontiers in Bioscience, vol. 12, no. 1, pp. 2447–2456, 2007. View at: Publisher Site | Google Scholar
  81. H. Ohnishi, T. Oka, S. Kusachi et al., “Increased expression of connective tissue growth factor in the infarct zone of experimentally induced myocardial infarction in rats,” Journal of Molecular and Cellular Cardiology, vol. 30, no. 11, pp. 2411–2422, 1998. View at: Publisher Site | Google Scholar
  82. Y. Nakamura, N. Patrushev, H. Inomata et al., “Role of protein tyrosine phosphatase 1B in vascular endothelial growth factor signaling and cell–cell adhesions in endothelial cells,” Circulation Research, vol. 102, no. 10, pp. 1182–1191, 2008. View at: Publisher Site | Google Scholar
  83. A. Qiao, A. Khechaduri, R. Kannan Mutharasan, R. Wu, V. Nagpal, and H. Ardehali, “MicroRNA‐210 decreases heme levels by targeting ferrochelatase in cardiomyocytes,” Journal of the American Heart Association, vol. 2, no. 2, article e000121, 2013. View at: Publisher Site | Google Scholar
  84. K. Cawley, S. E. Logue, A. M. Gorman et al., “Disruption of microRNA biogenesis confers resistance to ER stress-induced cell death upstream of the mitochondrion,” PLoS One, vol. 8, no. 8, article e73870, 2013. View at: Publisher Site | Google Scholar
  85. Y. L. Liu, S. O. Ang, D. A. Weigent, J. T. Prchal, and J. R. Bloomer, “Regulation of ferrochelatase gene expression by hypoxia,” Life Sciences, vol. 75, no. 17, pp. 2035–2043, 2004. View at: Publisher Site | Google Scholar
  86. K. Takeda, T. Tanaka, W. Shi et al., “Essential role of Stat6 in IL-4 signalling,” Nature, vol. 380, no. 6575, pp. 627–630, 1996. View at: Publisher Site | Google Scholar
  87. L. Huang, Q. Ma, Y. Li, B. Li, and L. Zhang, “Inhibition of microRNA-210 suppresses pro-inflammatory response and reduces acute brain injury of ischemic stroke in mice,” Experimental Neurology, vol. 300, pp. 41–50, 2018. View at: Publisher Site | Google Scholar
  88. S. M. Gysler, M. J. Mulla, M. Guerra et al., “Antiphospholipid antibody-induced miR-146a-3p drives trophoblast interleukin-8 secretion through activation of Toll-like receptor 8,” Molecular Human Reproduction, vol. 22, no. 7, pp. 465–474, 2016. View at: Publisher Site | Google Scholar
  89. G. Spinetti, E. Sangalli, C. Specchia et al., “The expression of the BPIFB4 and CXCR4 associates with sustained health in long-living individuals from Cilento-Italy,” Aging, vol. 9, no. 2, pp. 370–380, 2017. View at: Publisher Site | Google Scholar
  90. J. Liu, J. Mu, C. Zheng et al., “Systems-pharmacology dissection of traditional Chinese medicine compound saffron formula reveals multi-scale treatment strategy for cardiovascular diseases,” Scientific Reports, vol. 6, no. 1, article 19809, 2016. View at: Publisher Site | Google Scholar
  91. V. Ghorbanzadeh, M. Mohammadi, H. Dariushnejad, A. Abhari, L. Chodari, and G. Mohaddes, “Cardioprotective effect of crocin combined with voluntary exercise in rat: role of mir-126 and mir-210 in heart angiogenesis,” Arquivos Brasileiros de Cardiologia, vol. 109, no. 1, pp. 54–62, 2017. View at: Publisher Site | Google Scholar
  92. D. Zhao, H. Liu, and P. Dong, “Antihypertensive effect of azilsartan versus olmesartan in patients with essential hypertension: a meta-analysis,” Irish Journal of Medical Science, vol. 188, no. 2, pp. 481–488, 2018. View at: Publisher Site | Google Scholar
  93. X. Lu, Y. W. Bi, and K. B. Chen, “Olmesartan restores the protective effect of remote ischemic perconditioning against myocardial ischemia/reperfusion injury in spontaneously hypertensive rats,” Clinics, vol. 70, 7 pages, 2015. View at: Publisher Site | Google Scholar
  94. J. Liu, K. H. Narsinh, F. Lan et al., “Early stem cell engraftment predicts late cardiac functional recovery: preclinical insights from molecular imaging,” Circulation: Cardiovascular Imaging, vol. 5, no. 4, pp. 481–490, 2012. View at: Publisher Site | Google Scholar
  95. H. W. Kim, H. K. Haider, S. Jiang, and M. Ashraf, “Ischemic preconditioning augments survival of stem cells via miR-210 expression by targeting caspase-8-associated protein 2,” Journal of Biological Chemistry, vol. 284, no. 48, pp. 33161–33168, 2009. View at: Publisher Site | Google Scholar
  96. J. Nanduri, G. Yuan, G. K. Kumar, G. L. Semenza, and N. R. Prabhakar, “Transcriptional responses to intermittent hypoxia,” Respiratory Physiology & Neurobiology, vol. 164, no. 1-2, pp. 277–281, 2008. View at: Publisher Site | Google Scholar
  97. H. W. Kim, S. Jiang, M. Ashraf, and K. H. Haider, “Stem cell-based delivery of hypoxamir-210 to the infarcted heart: implications on stem cell survival and preservation of infarcted heart function,” Journal of Molecular Medicine, vol. 90, no. 9, pp. 997–1010, 2012. View at: Publisher Site | Google Scholar
  98. T. Wen, L. Wang, X. J. Sun, X. Zhao, G. W. Zhang, and J. Li-Ling, “Sevoflurane preconditioning promotes activation of resident CSCs by transplanted BMSCs via miR-210 in a rat model for myocardial infarction,” Oncotarget, vol. 8, no. 70, pp. 114637–114647, 2017. View at: Publisher Site | Google Scholar
  99. X. Ma, J. Wang, J. Li et al., “Loading miR-210 in endothelial progenitor cells derived exosomes boosts their beneficial effects on hypoxia/reoxygeneation-injured human endothelial cells via protecting mitochondrial function,” Cellular Physiology and Biochemistry, vol. 46, no. 2, pp. 664–675, 2018. View at: Publisher Site | Google Scholar
  100. N. M. Kane, M. Meloni, H. L. Spencer et al., “Derivation of endothelial cells from human embryonic stem cells by directed differentiation: analysis of microRNA and angiogenesis in vitro and in vivo,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 30, no. 7, pp. 1389–1397, 2010. View at: Publisher Site | Google Scholar
  101. J. Xu, Z. Y. Huang, L. Lin et al., “miR-210 over-expression enhances mesenchymal stem cell survival in an oxidative stress environment through antioxidation and c-Met pathway activation,” Science China Life Sciences, vol. 57, no. 10, pp. 989–997, 2014. View at: Publisher Site | Google Scholar
  102. L. Barile, V. Lionetti, E. Cervio et al., “Extracellular vesicles from human cardiac progenitor cells inhibit cardiomyocyte apoptosis and improve cardiac function after myocardial infarction,” Cardiovascular Research, vol. 103, no. 4, pp. 530–541, 2014. View at: Publisher Site | Google Scholar
  103. S. G. Ong, W. H. Lee, M. Huang et al., “Cross talk of combined gene and cell therapy in ischemic heart disease: role of exosomal microRNA transfer,” Circulation, vol. 130, Supplement 1, no. 11, pp. S60–S69, 2014. View at: Publisher Site | Google Scholar
  104. C. Emanueli, A. I. U. Shearn, A. Laftah et al., “Coronary artery-bypass-graft surgery increases the plasma concentration of exosomes carrying a cargo of cardiac microRNAs: an example of exosome trafficking out of the human heart with potential for cardiac biomarker discovery,” PLoS One, vol. 11, no. 4, article e0154274, 2016. View at: Publisher Site | Google Scholar

Copyright © 2019 Yinuo Guan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.