Review Article

MicroRNA as a Therapeutic Target in Cardiac Remodeling

Table 6

Summary of reported miRNAs and their targets in angiogenesis.

miRNAsTargetsEffector cellsSignal pathwaysReferences

Proangiogenesis
miR-126Spred-1HEPCsVEGF
PIK3R2HEPCsVEGF[156, 157]
CCN1HEPCsTEN/AKT

miR-130aGAXHUVECs and EGM-2Transcription
HOXA5HUVECs and EGM-2Transcription[158, 159]
PTENMI mousePI3K/Akt

miR-17–92 clusterTsp1HUVECsVEGF
CTGFHUVECsTGFβ[160]
BMP4HUVECsBmp4/Smad

miR-210Ephrin-A3,HUVECsVEGF[81, 161, 162]
PTP1bMHL-1CsVEGF

miR-146aVEGFhMSCsShh[65]

miR-296HGSHBMVECs[163]

miR-378SuFuU87 cellsShh[164, 165]
Fus-1U87 cellsShh

miR-132p120RasGAPHUVECsRas[166]

miR-23/27Sprouty2,HUVECsERK-MAPK [167]
Sema6AHUVECsVECF

miR-27bDll4,LLC1 and ATCCDll4/Notch [168]
PPARγLLC1 and ATCCPPAR

miR-24GATA2,HVSMCs and HUVECscGMP-PKG[169, 170]
PAK4HVSMCs and HUVECsTGF-β1/Smads
eNOSMI mouse, HUVECs and HMVECsPI3K/Akt

Antiangiogenesis
miR-214XBP1HUVECsVEGF[171]

miR-34 familySIRT1HUVECs, HMVECs and HAECsAMPK[172174]
vinculinLNA-antimiR-34–treated MI mice and H9c2 cellFAK1
Pofut1LNA-antimiR-34–treated MI mice and H9c2 cellNotch
Notch1LNA-antimiR-34–treated MI mice and H9c2 cellNotch
VEGFLNA-antimiR-34–treated MI mice and H9c2 cellVEGF
Sema4bLNA-antimiR-34–treated MI mice and H9c2 cellVECF

miR-29a/101aTGFb-1MI ratsTGFb pathway[175]

miR-15b-5pAKT3HUVECsPI3K-Akt[176]

miR-100mTORESMCs, VSMCsmTOR[177]

miR-200bZEB1/SIP1MDCKCs and HBCCsmTOR[178181]
GATA2Dermal wound-edge ECsVEGF
VEGFR2Dermal wound-edge ECsVEGF
Flt1HUVECsVEGF
KDRHUVECsVEGF

miR-503cdc25AHUVECs, HMVECs and HVSMCsMAPK [182]
CCNE1HUVECs, HMVECs and HVSMCsNotch

miR-15aFGF2HUVECsPI3K-AKT[183, 184]
VEGFHUVECsVEGF

miR-320IGF-1MCECs, NRCMsPI3K-Akt[185, 186]
Hsp20MCECs, NRCMsRNA degradation
Ets2MCECs, NRCMsPI3K-Akt

miR-329CD146HUVECs, HMECsVEGF and TNF-α[187]

miR-92aITGA5RMUG-S, OVISE and RMG-1Rho/ROCK[188190]

CCNE1: cyclin E1; cdc25A: cell division cycle 25A; CTGF: connective tissue growth factor; Dll4: delta-like protein 4; eNOS: endothelial nitric oxide synthase; Ets2: Euro Truck Simulator 2; FGF2: fibroblast growth factor 2; FGFR1: fibroblast growth factor receptor 1; GATA2: GATA binding protein 2; GAX: gaseous oxygen; HGS: hepatocyte growth factor-regulated tyrosine kinase substrate; HOXA5: homeobox A5; IGF-1: insulin-like growth factor 1; ITGA5: integrin subunits a5; mTOR: mechanistic target of rapamycin; PIK3R2: phosphoinositol-3 kinase regulatory subunit 2; Pofut1: protein O-fucosyltransferase 1; Pparγ: peroxisome proliferator-activated receptor γ; PTEN: phosphatase and tensin homolog; Sema4b: semaphorin 4B; Sema6A: semaphorin 6A; SIP1: Smad interacting protein 1; SIRT1: Sirtuin 1; Sprouty2: sprouty homolog 2; Tsp1: thrombospondin-1; VEGF: vascular endothelial growth factor; VEGFR2: vascular endothelial growth factor receptor 1; XBP1: X-box binding protein 1; ZEB1: zinc finger E-box-binding homeobox 1; FAK: focal adhesion kinase; HUVECs: human umbilical vein ECs; EGM-2: endothelial growth medium 2; MHL-1Cs: mouse HL-1 cardiomyocytes; hMSCs: human mesenchymal stem cells; Shh: sonic hedgehog signaling; HBMVECs: human brain microvascular endothelial cells; LLC1: Lewis lung carcinoma; ATCC: RAW 264.7 mouse macrophage cell lines; HVSMCs: human vascular smooth muscle cells; HUVECs: human umbilical vein endothelial cells; HMVECs: human microvascular ECs; HAECs: human aortic endothelial cell; ESMCs: endothelial smooth muscle cells; VSMCs: vascular smooth muscle cells; HVSMCs: human VSMCs cells; MDCKCs: Madin-Darby canine kidney cells; HBCCs: human breast cancer cells; dermal wound-edge ECs: dermal wound-edge endothelial cells; MCECs: mouse cardiac endothelial cells; NRCMs: neonatal rat cardiomyocytes; HMECs: human microvascular endothelial cells.