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Research Article | Open Access
Su-Lim Kim, Hack Sun Choi, Ji-Hyang Kim, Dong Kee Jeong, Ki-Seok Kim, Dong-Sun Lee, "Dihydrotanshinone-Induced NOX5 Activation Inhibits Breast Cancer Stem Cell through the ROS/Stat3 Signaling Pathway", Oxidative Medicine and Cellular Longevity, vol. 2019, Article ID 9296439, 16 pages, 2019. https://doi.org/10.1155/2019/9296439
Dihydrotanshinone-Induced NOX5 Activation Inhibits Breast Cancer Stem Cell through the ROS/Stat3 Signaling Pathway
Cancer stem cells (CSCs) are known to mediate metastasis and recurrence and are therefore a promising therapeutic target. In this study, we found that dihydrotanshinone (DHTS) inhibits CSC formation. DHTS inhibited mammosphere formation in a dose-dependent manner and showed significant tumor growth inhibition in a xenograft model. This compound reduced the CD44high/CD24low- and aldehyde dehydrogenase- (ALDH-) expressing cell population and the self-renewal-related genes Nanog, SOX2, OCT4, C-Myc, and CD44. DHTS induced NOX5 activation by increasing calcium, and NOX5 activation induced reactive oxygen species (ROS) production. ROS production reduced the nuclear phosphorylation levels of Stat3 and secreted IL-6 levels in the mammospheres. DHTS deregulated the dynamic equilibrium from non-stem cancer cells to CSCs by dephosphorylating Stat3 and decreasing IL-6 secretion and inhibiting CSC formation. These novel findings showed that DHTS-induced ROS deregulated the Stat3/IL-6 pathway and induced CSC death. NOX5 activation by DHTS inhibits CSC formation through ROS/Stat3/IL-6 signaling, and DHTS may be a promising potential therapeutic agent against breast CSCs.
Breast cancer is a common cancer and a leading cause of cancer death among women . Although widespread mammography and adjuvant therapy with polychemotherapy and tamoxifen for early breast cancer have reduced the mortality of breast cancer [2, 3], breast cancer is the most dangerous disease due to recurrence and metastasis. CSCs were first identified in leukemia  and were later found at various solid tumors . CSCs are known as cancer stem-like cells. Additionally, various types of cancer were originated from CSCs [6–8]. This subpopulation changes into tumor through self-renewal and differentiation [9, 10]. The Sonic hedgehog (Shh), Stat3, nuclear factor-κB (NF-κB), Wnt/β-catenin, TGF-β, and Notch signaling pathways are critical self-renewal factors of CSCs [11–14]. CSCs have drug resistance and radioresistance properties resulting in recurrence of cancer . Therefore, targeting of CSCs is important in cancer therapy. CSCs express specific proteins, including Oct4, Sox2, Nanog, and aldehyde dehydrogenase-1 (ALDH) . ALDH refers to a group of enzymes that oxidizes genotoxic aldehyde, and the ALDH activity is used as a CSC marker of leukemia and head and neck, bladder, bone, colon, liver, lung, pancreatic, prostate, thyroid, and cervical cancers . ALDH is also a therapeutic target of CSCs . The subpopulation of breast cancer expressing CD44high/CD24low in clinical specimens had a high capacity to form tumors . Signal transducer and activators of transcription 3 (Stat3) are frequently activated in CSCs, and mammosphere formation is related to the JAK1/2-Stat3 pathway. Secreted IL-6 activates the JAK1/2-Stat3 pathway and upregulates Oct4 gene expression. The IL-6/JAK1/2/STAT3 signaling pathway plays an important role in the conversion of non-stem cancer cells (NSCCs) into CSCs . Blocking the Stat3 signaling pathway inhibits the growth of CD44high/CD24low stem cell-like breast cancer cells . The NF-κB transcription factor is constitutively activated in tumor cells, including colon, breast, and liver cancers , and is regulated by the IκB kinase (IKK) complex. The NF-κB-specific inhibitor pyrrolidine dithiocarbamate (PDTC) inhibits breast cancer stem-like cells .
Reactive oxygen species (ROS) production of cancer cells occurs via multiple mechanisms, and ROS are produced in the mitochondria and by NADPH oxidase (NOX). ROS can play dual functions as important mediators and signal molecules or as damaging factors. As breast CSCs produce lower levels of ROS than tumor cells do, breast cancer stem-like cells are radioresistant . Because ROS are a major mediator of ionizing radiation-induced cell death, CSCs showed less DNA damage than NSCCs did . NOX is a ROS-generating enzyme that can be found not only within the plasma membrane [NOX1–5 and dual oxidase (DUOX) 1-2] but also in the endoplasmic reticulum (NOX2, NOX4, and NOX5), mitochondrial membrane (NOX4), and nuclear membrane (NOX4 and NOX5), as well as in the specialized membrane microdomains caveolin and lipid rafts (NOX1) . NOX5 has Ca2+-binding EF hands in the N-terminal. Compared with those of the other NOX members, the function and regulation of NOX5 in tumorigenesis and CSCs are largely unknown.
Dihydrotanshinone (DHTS) is a component of the well-known traditional Chinese medicinal plant Salvia miltiorrhiza and is used to treat cardiovascular disease, hepatitis, inflammation, and cancer [26, 27]. Previous studies have shown that DHTS has various biological functions, including liver protection, anti-inflammation, osteoclast differentiation, and tumor cell apoptosis [26, 28–31]. Although DHTS is effective in human cancer cell apoptosis, the exact mechanism of cancer cell apoptosis is poorly understood. In this study, we found that DHTS can selectively inhibit breast CSCs through NOX5/ROS/Stat3/IL-6 signaling and may be a promising potential therapeutic agent against breast CSCs.
2. Materials and Methods
Tissue culture plates, including 6- and 24-well ultralow attachment cluster plates, were obtained from Corning (Tewksbury, MA, USA). DHTS I, crytotanshinone, tanshinone I, and tanshinone II A were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA). Cell growth was assayed using a CellTiter 96® AQueous One Solution kit (Promega, Madison, WI, USA). The ALDEFLUOR™ Kit was obtained from STEMCELL Technologies Inc. (Vancouver, BC, Canada). Chemicals such as MβCD were obtained from Sigma-Aldrich Co. (St. Louis, MO, USA).
2.2. Cell Culture and Mammosphere Formation
Two cancer cell lines, MCF-7 and MDA-MB-231, were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). We followed the method of . Two cancer cell lines were grown in Dulbecco’s modified essential medium (DMEM; HyClone, Logan, UT, USA) with 10% fetal bovine serum (FBS; HyClone), 100 U/mL penicillin, and 100 μg/mL streptomycin (HyClone). Two breast cancer cell lines were maintained at 37°C in a humidified incubator with 5% CO2. Cells were plated at a density of cells in T75 culture flasks. For mammosphere formation, single cell-suspended cancer cell lines were seeded at a density of (MCF-7) and cells (MDA-MB-231)/well in ultralow-attachment 6-well plates containing 2.5 mL of complete MammoCult™ Medium (Stemcell Technologies). Two breast cancer cell lines were incubated in a 5% CO2 incubator at 37°C for 7 days.
2.3. Automated Counting of Mammospheres
We followed the method of . At 7 days of culture, a color scale image of the mammospheres was acquired by placing the culture plate on a scanner (PowerLook 1100, UMAX, Seattle, WA, USA). Images at resolutions of 300 or 600 dpi were analyzed using the software program NICE downloaded from https://www.nist.gov/services-resources/software/nists-integrated-colony-enumerator-nice . For counting, regions of interest were created by choosing the desired number of rows and columns (e.g., for a 6-well plate), and regions of interest were determined by moving and resizing the individual regions after selecting the elliptical setting and the selected images were automatically counted. The mammosphere formation was calculated by the mammosphere formation efficiency (MFE, %), which corresponds to the number of mammospheres per well/the number of total cells per .
2.4. Cell Proliferation
A CellTiter 96® Aqueous One Solution assay kit was used to measure the proliferation rate of MCF-7 and MDA-MB-231 cells. We followed the method of  Two breast cancer cells were cultured in a 96-well plate in the presence of DHTS (0.25, 0.5, 1, 2, and 4 μM) for 24 h. We followed the manufacturer’s protocol, and the optical density was determined by using a plate reader (Dynex Revelation, Dynex Ltd., Billingshurst, UK). Each series of data were determined in triplicate.
2.5. Colony Formation
MDA-MB-231 cells were seeded at a low density in a 6-well plate and treated with 1 μM DHTS. After 1 day, the media were replaced with fresh media and cultured for 10 days. The grown colonies were counted. We followed the method of .
2.6. Cell Migration
MDA-MB-231 cells were seeded in a 6-well plate and grown at 90% confluency. The scratch was made through the cell layer using a sterile white micropipette tip. After the samples were washed with new media, breast cancer cells were treated with DHTS. We followed the method of . Wounded areas were photographed with a light microscope at 10x after 16 h.
2.7. Flow Cytometric Analysis of CD44 and CD24 Expression
Expression of CD44 and CD24 was determined by FACS analysis in MDA-MB-231 cells. We followed the method of . After the cells were harvested and dissociated using 1x Trypsin/EDTA, one million cells were suspended and labeled with FITC-conjugated anti-human CD44 and PE-conjugated anti-human CD24 antibodies (BD Pharmingen, San Diego, CA, USA) and incubated at 4°C for 20 min. Then, the cells were washed three times with 1x PBS and analyzed by flow cytometry (Accuri C6, BD, San Jose, CA, USA).
2.8. Measurement of ROS Activity Using DCFDA (2,7-Dichlorofluorescein Diacetate) and the CellROX Green Dye Detection Method
Cancer cells were cultured in 96-well cell imaging plates and treated with DHTS (1 μM) or DMSO for 24 h. ROS were detected using DCFDA. DHTS-treated cancer cells were cultured, and the media were aspirated. The cancer cells were washed with 1x PBS and incubated with PBS containing 10 μM DCFDA dye and 5 μM CellROX Green for 30 min at room temperature. DCFDA and CellROX Green dye solution were removed and washed with 1x PBS. Finally, 0.1 mL PBS was added to 96-well plates, and the samples were observed under a phase-contrast fluorescence microscope (Lionheart FX live cell imager, Biotek, Winooski, VT, USA).
2.9. Calcium Assay Using the Fluo-4 NW Dye
A Fluo-4 NW calcium assay kit was used to measure the calcium levels of two breast cancer cell lines. The two breast cancer cell lines were grown in a 96-well plate in the presence of DHTS (0, 2, and 4 μM) for 24 h. We followed the manufacturer’s protocol (Molecular Probes, Wisconsin, USA), and 100 μL of the dye loading solution was added to a 96-well plate containing breast cancer cells. The plate was incubated at 37°C for 30 min, and the relative fluorescence was recorded using a flow cytometer (Accuri C6, BD, San Diego, CA, USA) and a phase-contrast fluorescence microscope (Lionheart FX live cell imager, Biotek).
2.10. Aldehyde Dehydrogenase (ALDH) Activity
ALDH activity was measured using a commercial ALDEFLUOR kit (Stemcell Technologies, Vancouver, BC, Canada). We followed the method of . The ALDH inhibitor diethylaminobenzaldehyde (DEAB) was used as a negative control. The breast cancer cells were treated with 1 μM DHTS for 1 day, and ALDH-positive cells were analyzed with the ALDEFLUOR assay. ALDH-positive and ALDH-negative cells were assayed using flow cytometry (Accuri C6, BD, San Diego, CA, USA).
2.11. RT-PCR and Real-Time RT-PCR
Total RNA was isolated using TaKaRa MiniBEST (TaKaRa, Tokyo, Japan) according to the supplier’s protocol. We followed the method of . For RT-PCR, 1 μg of total RNA was used for RT-PCR using the One-Step RT-PCR reagent (Qiagen, Germantown, MD, USA). The PCR cycle conditions consisted of 95°C for 0.5 min, 60°C for 0.5 min, and 72°C for 0.5 min followed by a 10 min extension at 72°C. Primers specific to NOX1–NOX5, DUOX1, and DUOX2 mRNAs were as follows: NOX1 primers (P197757_F and P197757; Bioneer, Daejeon, South Korea), NOX2 primers (P301247-F and P301247-R; Bioneer, Daejeon, South Korea), NOX3 primers (P225943_F and P225943_R; Bioneer, Daejeon, South Korea), NOX4 primers (P176436_F and P176436_R; Bioneer, Daejeon, South Korea), NOX5 primers (P210846_F and P210846_R; Bioneer, Daejeon, South Korea), DUOX1 primers (P218762_F and P218762_R; Bioneer, Daejeon, South Korea), and DUOX2 primers (P294520_F and P197757; Bioneer, Daejeon, South Korea). Primers for human β-actin, 5-TGTTACCAACTGGGACGACA-3 and 5-GGGGTGTTGAAGGTCTCAAA-3, were used as an internal control. The levels of transcripts also were determined by a One Step PrimeScript RT-PCR kit using SYBR Green according to the manufacturer’s instructions (TaKaRa, Tokyo, Japan). One-step RT-PCR reaction was carried out in 100 ng of total RNA, 10 μL of 2x One Step RT-PCR Buffer, 1 μL PrimeScript 1 step Enzyme Mix, and 10 μM of PCR forward primer and reverse primer of CD 44 (forward: 5-AGAAGGTGTGGGCAGAAGAA-3, reverse: 5-AAATGCACCATTTCCTGAGA-3), NANOG (forward: 5-ATGCCTCACACGGAGACTGT-3, reverse: 5-AAGTGGGTTGTTTGCCTTTG-3), OCT4 (forward: 5-AGCAAAACCCGGAGGAGT-3, reverse: 5-CCACATCGGCCTGTGTATATC-3), SOX2 (forward: 5-TTGCTGCCTCTTTAAGACTAGGA-3, reverse: 5-CTGGGGCTCAAACTTCTCTC-3), c-Myc (forward: 5-AATGAAAAGGCCCCCAAGGTAGTTATCC-3, reverse: 5-AGCAAAACCCGGAGGAGT-3), and β-actin (forward: 5-TGTTACCAACTGGGACGACA-3, reverse primer: 5-GGGGTGTTGAAGGTCTCAAA-3) for a final volume of 25 μL per reaction. The relative mRNA expression levels of the target genes were calculated using the comparative CT values. At least four independent PCR procedures were performed to allow for statistical analysis. The PCR products were normalized to that of the β-actin gene as an internal control.
2.12. Western Blot Analysis
We followed the method of . Proteins isolated from mammospheres treated with DHTS were separated on 10% SDS-PAGE and transferred to a polyvinylidene difluoride membrane (Millipore, Bedford, MA, USA). PVDF membranes were blocked in 3% bovine serum albumin (BSA) in PBS-Tween 20 (0.1%, v/v) at room temperature for 1 hour. The PVDF membranes were incubated in blocking solution with primary antibodies at 4°C overnight. The primary antibodies used were Stat3, p65, lamin B (Santa Cruz Biotechnology), pStat3 (Cell Signaling, Beverly, MA, USA), and NOX2 (AB Frontier, Seoul, Korea). An antibody against β-actin (Santa Cruz Biotechnology) was used as a control. After PVDF membranes were washed with PBS-Tween 20 (0.1%, v/v), the membranes were incubated with HRP-conjugated secondary antibodies and enhanced using the chemiluminescence detection kit (Santa Cruz Biotechnology, Santa Cruz, CA, USA).
2.13. Electrophoretic Mobility Shift Assays (EMSA)
We followed the method of . EMSA was analyzed using a chemiluminescent EMSA kit according to the manufacturer’s protocol (Thermo Scientific, IL, USA). The biotin upper and lower strands of the Stat3 probe (5-CTTCATTTCCCGGAAATCCCTA-Biotin-3 and 5-TAGGGATTTCCGGGAAATGAAG-Biotin-3) were synthesized. Nuclear extracts were isolated from two breast cancer cells as described previously . The biotin-labeled probes were incubated with DHTA-treated nuclear proteins in a final volume of 20 μL EMSA buffer containing poly[dI-dC] for 30 min. The mixtures were electrophoresed on a 6% native PAGE gel in 0.5x TBE at 4°C and visualized using a chemiluminescent nucleic acid detection kit (Thermo Scientific, Waltham, MA USA).
2.14. Small Interfering RNA (siRNA)
To determine the effect of NOX2 and NOX5 on mammosphere formation, we treated MDA-MB-231-derived mammospheres with human NOX2 siRNA (NM_000397.3; Bioneer, Daejeon, South Korea) and NOX5 siRNA (NM_001184779.1; Bioneer, Daejeon, South Korea) (or scrambled siRNA control; Bioneer, Daejeon, South Korea). For transfection of the siRNA, the cancer cells were seeded into 6-well plates for 24 h, and transfection was performed using Lipofectamine 2000 (Thermo Scientific) according to the manufacturer’s protocol. The levels of NOX2 and NOX5 protein were determined by western blot analyses using anti-NOX2 and anti-NOX5 antibodies.
2.15. Chemotherapy of the Breast Cancer Cell-Bearing Immunodeficient BALB/C Nude Female Nude Mice
Female BALB/C nude mice (4–5 weeks old) were purchased from Orient Bio (Seongnam, Korea) and kept in animal facilities for 1–2 weeks. A total of 14 breast cancer cell-bearing BALB/C female nude mice were divided into two groups. The 7 mice in the negative control group received no chemotherapy. However, the volumes of control mouse tumors were measured every three days and then calculated using the formula (width2 × length)/2 (Figure 2). Seven nude mice received DHTS using mammary fat pad injection with an optimized dosage of 10–50 mg/kg. All animal experiments and procedures were conducted with a protocol approved by the Institutional Animal Care and Use Committee of Jeju National University. At the end of the experiment, mice were sacrificed, and tumor specimens were taken, photographed, and weighed.
2.16. Statistical Analysis
All data are presented as deviation (SD). Data were analyzed using Student’s -test. A value lower than 0.05 was considered statistically significant (GraphPad Prism 5 Software, San Diego, CA, USA).
3.1. Effect of Tanshinones on Mammosphere Formation in Breast Cancer Cells
To evaluate whether tanshinones can suppress the formation of the mammosphere, we added different concentrations of tanshinones to the MCF-7- and MDA-MB-231-derived mammospheres. As shown in Figure 1(a), DHTS produced the most potent inhibitory effect on mammosphere formation. DHTS inhibited the formation of primary mammospheres derived from MCF-7 and MDA-MB-231 cancer cells. Not only were the numbers of mammospheres decreased by 50% to 95% but also the size of the mammospheres was decreased (Figure 1(c)). We examined the proliferative effect of DHTS on two breast cancer cells by MTS assays. There was inhibition of cell proliferation with ≥2 μM (MDA-MB-231 and MCF-7 cells) after 24 h of stimulation (Figure 1(b)). DHTS inhibited the migration and colony formation of MDA-MB-231 cells (Figures 1(d) and 1(e)).
3.2. DHTS Inhibits Tumor Growth in a Xenograft Model
As DHTS showed antiproliferative effects on breast cancer cells in vitro, we examined whether DHTS inhibited tumorigenicity in a xenograft tumor model. The tumor volume in the DHTS-treated group was smaller than that in the control group (Figures 2(a) and 2(b)). Additionally, tumor weights in the DHTS-treated group were lower than those in the control group (Figure 2(c)). Mice in the DHTS-treated group and control group showed similar body weights (Figure 2(a)). These results demonstrated that DHTS effectively inhibited tumorigenicity in a xenograft model.
3.3. Effect of DHTS on Proportion of CD44high/CD24low- and ALDH-Expressing Breast Cancer Cell Line
MDA-MB-231 cells were treated with DHTS for 1 day, and the CD44high/CD24low-expressing population of cancer cells was investigated. DHTS decreased the CD44high/CD24low-expressing population of MDA-MB-231 cancer cells (Figure 3(a)). MDA-MB-231 cells were subjected to an ALDEFLUOR assay to investigate the effect of DHTS on the proportion of ALDH-expressing cancer cells. DHTS decreased the proportion of ALDH-expressing cancer cells from 1.2% to 0.6% (Figure 3(b)). These results showed that DHTS effectively reduced expression of CSC markers.
3.4. DHTS Induces ROS Generation, and NAC Reverses DHTS-Induced Mammosphere Inhibition
Generally, increased ROS have been shown to kill CSCs, and low levels of ROS are associated with the stemness of stem cells and CSCs . We examined the levels of ROS in breast cancer cells under DHTS. As shown in Figure 4(a), DHTS induced ROS generation in a concentration-dependent manner in MDA-MB-231 cells. N-Acetylcysteine (NAC) reversed DHTS-induced ROS production. To determine whether DHTS-induced ROS inhibit mammosphere formation, we performed a mammosphere formation assay with NAC. NAC reversed DHTS-induced mammosphere inhibition (Figure 4(b)). ROS production plays an important role in DHTS-induced mammosphere death.
3.5. DHTS-Induced Mammosphere Formation Inhibition Is Dependent on NADH Oxidase
To test NOX-dependent ROS production, we determined the effect of the NOX inhibitor diphenyleneiodonium (DPI) on mammosphere formation. DPI pretreatment attenuated DHTS-induced mammosphere inhibition (Figure 4(c)). These results showed that NOX plays a key role in DHTS-mammosphere death and that DHTS is involved in the NOX-dependent pathway.
3.6. NOX5, but Not NOX2, Is Involved in DHTS-Induced ROS Production and DHTS-Induced Mammosphere Inhibition
We showed that DHTS regulates mammosphere formation through activation of ROS-generating NOX and then investigated which NOX regulates DHTS-induced mammosphere inhibition. We analyzed the mRNA expression of the NOX isoforms NOX1–5 and DUOX1–2 in MCF-7 and MDA-MB-231 cells and their mammospheres. Our data showed the expression of distinct isoforms of NOX2 and NOX5 in MCF-7 and MDA-MB-231 cells and their mammospheres (Figure 5(a)), and a previous paper showed similar data . The transcripts and proteins of NOX2 and NOX5 were distinctly expressed in breast cancer cells and mammospheres. The major NOX proteins are NOX2 and NOX5, and their protein levels under DHTS were not changed (Figure 5(b)). To test the effect of NOX2 and NOX5 on mammosphere formation, we performed siRNA-inducing silencing of NOX2 and NOX5 expression, which did not reduce the mammosphere formation in MDA-MB-231 cancer cells (Figures 5(c) and 5(d)). These results showed that NOX activation plays a key role in DHTS-induced mammosphere death. To assess DHTS-dependent mammosphere formation inhibition by NOX2 and NOX5, we used methyl-β-cyclodextrin (MβCD) for a functional study of NOX2 and NOX5. As a cholesterol-sequestering agent, MβCD can selectively and rapidly remove cholesterol and cause disruption of lipid rafts ; this molecule has been reported to possess free radical scavenging activity and to protect against oxidative stress caused by the addition of hydrogen peroxide . The NOX enzyme activity of breast cancer was decreased by MβCD . To select a proper concentration of MβCD for the mammosphere formation assays, we added MβCD to the mammospheres. We found that 1 mM of MβCD did not affect mammosphere formation, but 5 mM of MβCD dramatically inhibited mammosphere formation (Figure 5(e)). We tested the effect of DHTS on mammosphere formation using 1 mM MβCD. The inhibitory effect of DHTS on mammosphere formation was ameliorated by MβCD. These data showed that DHTS-induced ROS production was ameliorated by MβCD. To explain the relationship between NOX and ROS production, we tested the release of NOX proteins from the mammospheres. Our data showed that MβCD decreases the NOX5 protein level, but not the NOX2 level, in a concentration-dependent manner, and DHTS-dependent mammosphere formation inhibition is related to ROS production by NOX5 enzyme activation (Figures 5(f) and 5(g)).
3.7. Localization of ROS under DHTS in MDA-MB-231 Cells
To test the localization of ROS after DHTS treatment in breast cancer cells, we added DHTS to the cells and stained the cancer cells with the fluorogenic probe CellROX Green Reagent to visualize ROS. We examined the levels of ROS in breast cancer cells under DHTS. As shown in Figure 5(h), DHTS induced ROS generation in MDA-MB-231 cells. To determine where DHTS-induced ROS are located, we merged the ROS Green Reagent with the Hoechst nuclear dye. Our data showed that ROS are localized at the cell membrane (Figure 5(h)).
3.8. DHTS Triggers Mammosphere Death by ROS-Induced Calcium Release
Activation of the NOX5 enzyme requires calcium . We assessed calcium release under DHTS treatment using the Fluo-4 NW calcium assay method. DHTS induced calcium release from breast cancer cells in a concentration-dependent manner (Figure 6(a)). DHTS-induced calcium release was ameliorated by NAC (Figure 6(a)). These data showed that DHTS induced calcium release and then ROS production. We examined whether DHTS inhibits mammosphere formation using the calcium chelator BAPTA-AM. The number of DHTS-treated mammospheres was decreased, and DHTS and BAPTA-AM treatment ameliorated the inhibition of mammosphere formation (Figures 6(b) and 6(c)). These data showed that DHTS triggers mammosphere death by ROS-induced calcium release.
3.9. Effect of DHTS on the Stat3 Pathway Activation and Secreted IL-6 in Mammospheres
The ROS-mediated activation of the STAT3 signaling pathway was involved in cellular senescence . To determine the biological function of DHTS, we examined the Stat3 and NF-κB pathways in mammosphere-derived MDA-MB-231 cells under DHTS treatment. DHTS can reduce the nuclear pStat3 protein level compared to DMSO treatment. But DHTS could not reduce the nuclear p65 protein level (Figure 7(a)). We did EMSA to analyze Stat3/DNA binding using a Stat-binding oligonucleotide that binds Stat3 protein . As shown in Figure 7(b), DHTS reduced the ability of Stat3 protein to bind the Stat3 probe (Figure 7(b), lane 3). The specificity of the pStat3/Stat probe oligonucleotide was assayed using an excess unlabeled oligonucleotide self-competitor (Figure 7(b), lane 4) and a mutated-Stat oligonucleotide competitor (Figure 7(b), lane 5). These data suggest that DHTS inhibits the Stat3 signaling pathway. IL-6 cytokine plays an important role in the formation of mammosphere . To determine the level of secreted IL-6, we did Western blot analysis in mammosphere-cultured solution by using an anti-IL-6. After DHTS treatment, Western blot data indicated that DHTS reduced the level of secreted IL-6. An internal control was used to count numbers of cancer cell/well with/without DHTS (Figure 7(c)). To determine whether DHTS induces dephosphorylation of Stat3, we examined pStat3 levels with NAC. NAC could reverse DHTS-induced dephosphorylation of Stat3 (Figure 7(d)). These results showed that ROS/Stat3 signaling plays a key role in DHTS-induced mammosphere death.
3.10. Effect of DHTS on Transcriptional Levels of Self-Renewal Gene in CSCs and Proliferation of Mammospheres
To test whether DHTS regulates the transcriptional levels of self-renewal genes, we examined the transcriptional levels of self-renewal genes using by real-time RT-PCR. DHTS reduced the expression of self-renewal genes of Nanog, Sox2, Oct4, c-Myc, and CD44 in CSCs (Figure 7(e)). To assay whether DHTS regulates mammosphere growth, we treated DHTS on mammospheres, and cancer cell numbers were counted. DHTS killed cancer cells in the mammospheres, and a decreased cancer cell number was observed in DHTS-treated mammospheres. DHTS led to a decrease in mammosphere proliferation (Figure 7(f)).
Breast cancer is one of the major causes of morbidity and mortality in women. Although mortality of breast cancer has decreased due to widespread mammography screening and adjuvant therapy containing tamoxifen and chemotherapy, this cancer is a fatal disease in females . The CSCs are involved in self-renewal and differentiation, similar to normal stem cells, and contribute to drug resistance of cancer patients . The original CSC research was mainly based on leukemia stem cells. Solid tumor stem cells derived from breast cancer were isolated for the first time in 2003 . Many CSCs were isolated from cancer patients and cancer cell lines. As CSCs from cancer patients are limited, CSCs of cancer cell lines were useful in cancer research.
Our results show evidence for DHTS as an antitumor and anti-CSC agent of breast cancer: (1) DHTS inhibited the proliferation of breast cancer cells and the size and formation of the mammospheres (Figure 1); (2) DHTS inhibited cell migration and colony formation of cancer cells (Figure 1); (3) DHTS suppressed tumor growth of mice in vivo (Figure 2); (4) DHTS reduced the CD44high/CD24low and ALDH-positive populations in cancer cells (Figure 3); (5) DHTS inhibited mammosphere formation through ROS production, and DHTS-induced mammosphere inhibition was ameliorated by NAC (Figure 4); (6) A NOX inhibitor, DPI, ameliorated DHTS-induced mammosphere inhibition. The major NOX proteins of breast CSCs are NOX2 and NOX5, and DHTS induced mammosphere formation inhibition, which is dependent on NOX5 activation by calcium release (Figures 5 and 6). (7) DHTS inhibited the Stat3 signal pathway of the mammospheres (Figure 7). DHTS reduced the secretory IL-6 level, which is an important cytokine of CSCs (Figure 7) , and induced a decrease in mammosphere growth (Figure 7). DHTS can be an anticancer agent by targeting breast cancer and CSCs.
Recent studies have shown that DHTS inhibits breast adenocarcinoma through G1 arrest and apoptosis and induces ROS-dependent apoptosis in colon cancer cells [26, 48]. CSCs in human and mouse breast tumors have lower ROS levels than the corresponding nontumorigenic cells , and this low level of ROS seems to be associated with high expression of ROS-scavenging molecule . CSCs have a high antioxidant capacity to maintain cellular ROS and a strongly increased antioxidant property for CSC survival and drug resistance.
The NOX family is a group of transmembrane proteins able to transport electrons from NADPH and to reduce oxygen to the ROS superoxide anion (O2·−) and hydrogen peroxide (H2O2) . In mammals, NOX1 to NOX5 and DUOX1 and DUOX2 comprise the seven NOX proteins . Our data showed that NOX proteins of breast CSCs are primarily NOX2 and NOX5. DTHS-induced CSC inhibition occurs via the NOX5 enzyme. NOX5 activation is dependent on EF hands (helix-loop-helix motifs) that bind calcium ions . For the first time, we showed that NOX5 activation is essential for breast CSC death (Figure 6). ROS generated by NOX enzymes induced activation of Stat3 and autophagy of cancer cells . We assessed the Stat3 signal after DHTS-induced ROS production. DHTS inhibited the Stat3 signal of CSCs and IL-6 production (Figure 7). The Stat3 signaling pathway is a critical factor in the function of normal stem cells and plays an important role in breast CSCs. The nuclear translocation of phosphorylated Stat3 by DHTS was tested in breast mammospheres. We showed that DHTS reduced the nuclear translocation of phosphor-Stat3 (Figure 7(a)). Breast CSCs are resistant to different anticancer agents and responsible for breast cancer relapse. The constitutively activated phosphor-Stat3 is responsible for 30–60% of primary breast cancer. Our data indicated that DHTS reduced the protein levels of nuclear pStat3 and Stat3 DNA-binding activity. DHTS inhibited formation of mammosphere via the blocking of the Stat3 signaling pathway (Figure 7).
Tumors composed of multicellular types are heterogeneous: cancer cells, CSCs, cancer-associated fibroblasts, macrophages, and tumor-infiltrating lymphocytes. Solid tumors have CSCs and NSCCs, and equilibrium between CSCs and NSCCs is controlled by secreted IL-6 . The IL-6 antibody blocked the CSC formation . The cytokine IL-6 and IL-8 regulated self-renewal of CSCs . Blockade of secretory IL-6 using anti-IL-6 can be a useful tool for targeting CSCs. DHTS inhibited the secretion of IL-6 and can be a candidate for inhibition of IL-6 secretion in solid tumor (Figure 7). IL-6 is important in the formation of mammospheres. Because the presence of secretory IL-6 is correlated with a poor prognosis in cancer patients, the regulation of intratumoral IL-6 is important for cancer treatment .
DHTS is a naturally occurring compound extracted from S. miltiorrhiza, a Chinese medicinal plant, and has been reported to have cytotoxicity to a variety of tumor cells. DHTS has been shown to induce apoptosis via induction of endoplasmic reticulum stress . DHTS can target breast CSCs by blocking inflammatory pathways containing NOX5/ROS/Stat3 signaling and IL-6. Our data showed that DHTS may be used as a new breast cancer chemopreventive agent.
The data used to support the findings of this study are available from the corresponding author upon request.
Highlights. Dihydrotanshinone (DHTS) induced NOX5 activation by increasing calcium, and NOX5 activation induced reactive oxygen species (ROS) production. ROS production reduced the nuclear phosphorylation levels of Stat3 and secreted IL-6 levels in the mammospheres. DHTS deregulated the dynamic equilibrium from non-stem cancer cells to CSCs by dephosphorylating Stat3 and decreasing IL-6 secretion and inhibiting CSC formation. These novel findings showed that DHTS-induced ROS deregulated the Stat3/IL-6 pathway and induced CSC death. NOX5 activation by DHTS inhibits CSC formation through ROS/Stat3/IL-6 signaling, and DHTS may be a promising potential therapeutic agent against breast CSCs.
Conflicts of Interest
The authors declare no potential conflicts of interest with data presentation in this article.
Su-Lim Kim and Hack Sun Choi contributed equally to this work.
We thank Dr. William M. Nauseef for providing the NOX-5 antibody. This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF), which is funded by the Ministry of Education (NRF-2016R1A6A1A03012862 and NRF-2017R1A2B1011756).
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