Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway

Abstract

Background

Indirubin is the active component of Danggui Longhui Wan, a traditional Chinese medicine formulation. Due to its anti-inflammation and anti-tumor effects, indirubin has been widely used for the treatment of inflammation, cancer, and other chronic disease. Herein, we aimed to investigate the role and mechanism of indirubin in human ovarian cancer cell proliferation.

Materials and methods

The cell viability was determined by Cell Counting Kit-8 and colony formation assays by treatment with different dosages of indirubin over 72 hours. Apoptosis was examined by flow cytometry with fluorescein isothiocyanate Annexin V Apoptosis Detection Kit. Western blot assay was finally applied to analyze the expression of cancer-related STAT3 pathway and its downstream proteins.

Results

Indirubin was found to significantly inhibit cell viability and induce apoptosis in 2 human ovarian cancer cell lines. Mechanistic studies revealed that indirubin treatment led to reduced levels of phosphorylated-STAT3, thus repressing the downstream pro-survival proteins and elevating pro-apoptosis ones.

Conclusion

Our study provided the evidence for anti-survival activity of indirubin by inhibiting cell viability and inducing apoptosis in human ovarian cancer cells, which involved impaired STAT3 signaling pathway. Our findings further support indirubin as a potential drug candidate against human ovarian cancer.

Keywords:

• indirubin
• ovarian cancer
• cell viability
• STAT3 signaling

Introduction

Ovarian cancer is the most common and second lethal type of gynecological cancer affecting women worldwide.^1,2 Due to lack of evident symptoms, most of patients with ovarian cancer are diagnosed at the advanced stage, leading to a 5-year survival rate ranging from 25% to 30%.³ Besides, high recurrence rate and chemo-resistance also contribute to poor prognosis and high mortality among these patients.^4,5 Therefore, a refined investigation of the therapy strategies and identification of novel agents for ovarian cancer, especially high-grade ovarian cancer, are urgently required to improve the survival rate of this disease.

Till now, numerous natural products (mostly plant extracts) have been used to treat human diseases, including cancers.^6,7 They constitute the basis for multiple prescriptions in traditional Chinese medicine and appear as a complementary approach to treat cancers.⁸ Danggui Longhui Wan is a compound from traditional Chinese medicine consisting of 11 herbal medicines, and is used for treating chronic myeloid leukemia.⁹ Among the 11 medicinal ingredients, Qing Dai (indigo naturalis) appears to be closely associated with the anti-leukemic activity, which is composed of high levels of indigo dye and a minor but active component indirubin. It has been discovered that indirubin and its derivatives are strong inhibitors of cyclin-dependent kinases (CDKs) by competing with ATP binding at the catalytic site, resulting in G2/M arrest and apoptosis in cancer cells.^10,11 Indirubin derivative has been proved to inhibit tumor cell growth in many types of cancer cell lines and induced apoptosis.¹² Indirubin derivative E738 has been identified as a novel dual inhibitor of JAKs and SFKs, which leads to inhibition of STAT3 signaling.¹³ And indirubin derivative 6BIO has been reported to exert the unique property of increasing stress tolerance and, in parallel, partially suppressing the nutrient-sensing pathway signaling.¹⁴ Moreover, indirubin has been reported to decrease the susceptibility to influenza virus and promote the expression of interferon-β and interferon-inducible transmembrane 3 through promoting mitochondrial antiviral signaling pathway.¹⁵ Over the last 2 decades, numerous studies relevant to anti-tumor activity of indirubin have been reported in the literature. However, whether it possesses oncotherapy potential in ovarian cancer remains unclear.

In this study, we focus our work on investigating the effect of simple indirubin on cell survival, including cell proliferation and apoptosis, in 2 different ovarian cancer cell lines and elucidate the significant cytotoxic mechanisms of this compound against ovarian cancer cells.

Materials and methods

This work was approved by the review board of The First Affiliated Hospital of Fujian Medical University.

Cell culture and reagent

Human cervical cancer cell lines A2780 and OVCAR3 were purchased from the cell bank of Shanghai Institute of Biochemistry and Cell Biology (Shanghai, China). The cells were cultured in Roswell Park Memorial Institute 1640 medium with 10% fetal bovine serum (Thermo Fisher Scientific, Waltham, MA, USA), 100 U/mL of penicillin and 100 µg/mL of streptomycin (Thermo Fisher Scien tific) in a 5% CO₂ incubator at 37°C. Indirubin was purchased from Sigma-Aldrich (San Francisco, CA, USA). Colivelin was purchased from Santa Cruz Biotechnology (sc-361153, Santa Cruz, CA, USA).

Cell Counting Kit-8 (CCK-8) assay

Cell viability assay was performed by CCK-8 methods. Briefly, cells were seeded in 96-well plate overnight at a density of 2×10³ per well, and then treated with different concentrations of indirubin (2 and 5 µM) for 0, 24, 48, or 72 hours, respectively. After incubation, 10 µL Cell Counting Kit-8 (Dojindo, Tokyo, Japan) was added into each well for 1 hour. The OD of each sample was detected at 450 nm using a microplate reader. The experiments were performed in triplicate.

Colony formation assay

Cell viability assay was performed by colony formation assay and crystal violet staining methods. Briefly, the cells were seeded into a 6-well plate at 5×10³ per well. After 12 hours, the cells were treated with indirubin at the concentration of 5 µM at 37°C. The culture medium was refreshed every 2 days. Ten days later, the cells were washed twice with PBS and fixed in 4% paraformaldehyde for 30 minutes. After washing twice with PBS buffer, the cells were stained with 1% crystal violet staining buffer for 30 minutes. The plates were then aspirated, washed, and allowed to air dry, followed by photograph by digital camera.

Flow cytometry analysis

Cell apoptosis assay was conducted by flow cytometry with fluorescein isothiocyanate (FITC) Annexin V Apoptosis Detection Kit (BD Biosciences, San Jose, CA, USA) as per the manufacturer’s protocol. Briefly, the cells were treated with different concentrations of indirubin (0, 0.5, 1, 2, 5, 10, and 20 µM) for 72 hours, followed by harvesting and suspending in binding buffer at a concentration of 1.5×10⁶ cells/mL. Then, 5 µL FITC Annexin V and 5 µL propidium iodide staining solution were added to 200 µL of the cell suspension. The mixture was incubated for 30 minutes at room temperature in dark and cells apoptosis was detected by BD FACSVerse™ (BD Biosciences). Apoptosis rate of cancer cells were analyzed by BD FACSuite software.

Western blot assay

A2780 and OVCAR3 cells were treated with different concentrations of indirubin (2 and 5 µM) or pretreated with 0.5 µM colivelin. Forty-eight hours later, the cells were washed by PBS and harvested by RIPA buffer (Beyotime, Shanghai, China) with 1 mM phenylmethylsulfonyl fluoride (Beyotime) on ice for 30 minutes. After centrifuging at 13,000 g at 4°C for 15 minutes, the supernatant fractions were collected and the protein concentration was quantified using a BCA Protein Assay Kit (Beyotime). The remaining supernatant was mixed with 2× loading buffer and boiled at 100°C for 15 minutes. The same amounts of protein were separated using 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis and then transferred to nitrocellulose membrane (Millipore, Billerica, MA, USA). After transferring, the membrane was blocked with 5% fat-free milk in PBST (PBS with Tween 20). Primary antibodies were incubated at 4°C overnight, and secondary antibodies were incubated at room temperature for 1 hour. The membranes were washed in PBST and the proteins of interest were visualized using enhanced chemiluminescence Western blotting substrate (Pierce, Rockford, IL, USA). β-actin was used as an internal control. Anti-p-STAT (Tyr705) (1:1,000, #9145), anti-t-STAT3 (1:1,000, #9139), anti-Bcl-xL (1:1,000, #2764), anti-bax (1:1,000, #2774), anti-cleaved caspase 3 (1:1,000, #9664), and anti-β-actin (1:5,000, #3700) antibodies were from Cell Signaling Technology (San Jose, CA, USA). Anti-Cyclin D1 (1:1,000, sc-450) and anti-C-myc (1:1,000, sc-4084) antibodies were from Santa Cruz (Dallas, TX, USA).

Statistical analysis

All data were analyzed by GraphPad Prism 7.0 software. Comparison between groups was performed by one-way ANOVA followed by Student–Newman–Keuls test. The data were presented as mean ± SD. A P-value <0.05 was considered as statistically significant. All experiments were repeated thrice independently.

Results

Indirubin inhibits cell viability of human ovarian cancer cells

To characterize the cytotoxicity of indirubin on human ovarian cancer cells, we first treated 2 different ovarian cancer cell lines, A2780 and OVCAR3, with increasing dosages of indirubin (0, 0.5, 1, 2, 5, 10, and 20 µM) for 72 hours. Then cell viability was analyzed by CCK-8 assay. The results shown in Figure 1A revealed a similarly decreased cell viability following treatment with indirubin at >2 µM concentrations. And the half maximal inhibitory concentration value of indirubin for each cell line was ~4 µM. By treating the 2 cell lines with either 2 or 5 µM indirubin for 3 days continuously, we observed a similar time-dependent inhibition of cell viability, and that 5 µM indirubin made the faster suppression (Figure 1B and C). In addition, treatment with 5 µM indirubin significantly inhibited colony formation in both A2780 and OVCAR3 cell lines (Figure 1D). These results indicate that indirubin represses cell viability of ovarian cancer cells in vitro.

Figure 1 Indirubin inhibited cell viability in ovarian cancer cells.

Notes: (A) A2780 and OVCAR3 cells were incubated with indirubin at different concentrations (0, 0.5, 1, 2, 5, 10, and 20 µM) for 72 hours. (B, C) A2780 and OVCAR3 cells were exposed to indirubin (2 and 5 µM), respectively, for different time points (0, 24, 48, and 72 hours). Cell viability was measured using CCK-8 assays. (D) Colony formation assay of A2780 and OVCAR3 cells was treated with indirubin (2 and 5 µM), respectively. The right panel shows the quantitative results. Each experiment was performed in triplicate independently. The data are presented as mean ± SD. *P<0.05, **P<0.01, ***P<0.001 vs control group.
Abbreviation: CCK-8, Cell Counting Kit-8.

Indirubin induces apoptosis of human ovarian cancer cells

To examine whether indirubin represses cell viability via inducing cell apoptosis in the 2 ovarian cancer cell lines tested, we then evaluated the apoptosis rate of indirubin-treated cells through flow cytometry with FITC Annexin V Apoptosis Detection Kit. As shown in Figure 2A–C, after incubation with increasing concentrations of indirubin (0, 0.5, 1, 2, 5, 10, and 20 µM) for 72 hours, Annexin V-labeled cell apoptosis increased with the increased dosage of indirubin. These results suggested that indirubin treatment induces the apoptosis of ovarian cancer cells in vitro.

Figure 2 Indirubin induced apoptosis in ovarian cancer cells.

Notes: A2780 (A) and OVCAR3 (B) cells were treated with indirubin at different concentrations (0, 0.5, 1, 2, 5, 10, and 20 µM) for 72 hours. Flow cytometry analysis showed indirubin induced higher apoptosis with increasing doses of indirubin. (C) Early and late apoptotic events of A2780 cells treated without or with different dose of indirubin were detected by flow cytometry. Top left quadrant indicates non-apoptotic cells; top right quadrant represents late apoptosis events; bottom right quadrant represents early apoptosis cells; and bottom left quadrant represents living cells. Each experiment was performed in triplicate independently. The data are presented as mean ± SD. **P<0.01, ***P<0.001 vs control group.

Cell viability inhibitory effects of indirubin was associated with the inhibition of STAT3 signaling

To further explore the molecular mechanism of anti-viability action of indirubin, we investigated the effect of indirubin on the cancer-related STAT3 signaling pathway. We found that indirubin caused downregulation of phospho-STAT3 (Tyr705) dose-dependently in both A2780 and OVCAR3 cells (Figure 3A and B). As is known, STAT3, activated by phosphorylation, plays a key role as a critical transcription activator in cell proliferation. We then analyzed the expression of STAT3 downstream genes. Results showed that indirubin significantly inhibited the expression of Cyclin D1 and C-myc (Figure 3A and B). On the other hand, STAT3 is also involved in the inhibition of apoptosis. Consistently, we found that the pro-apoptosis Bax and cleaved caspase 3 were activated, whereas the anti-apoptotic Bcl-xL was repressed by indirubin in the 2 cell lines dose-dependently (Figure 4A and B). These findings suggested that indirubin exerts anti-viability effects by inhibiting the activation of STAT3 signaling.

Figure 3 Indirubin-mediated expression of survival-related protein altered.

Notes: (A) Western blot assay showed that indirubin downregulated the phosphorylated level of STAT3 and the expression of survival related protein Cyclin D1, C-myc with increasing concentrations in A2780 and OVCAR3 cells. Each experiment was performed in triplicate independently. (B) Quantitative results shown by ImageJ software. **P<0.01; ***P<0.001.

Figure 4 Indirubin-mediated expression of apoptosis-related protein altered.

Notes: (A) Western blot assay showed that indirubin downregulated the expression of anti-apoptosis protein Bcl-xL and upregulated pro-apoptosis protein Bax, cleaved caspase 3 with increasing concentrations in A2780 and OVCAR3 cells. Each experiment was performed in triplicate independently. (B) Quantitative results shown by ImageJ software. *P<0.05; **P<0.01; ***P<0.001.

Colivelin partly reversed the indirubin-induced suppression of cell viability and phosphorylation of STAT3

To investigate whether indirubin played anti-viability roles through the phosphorylation of STAT3, colivelin, a STAT3 activator, was used in our system. A2780 cells were pretreated with 0.5 µM colivelin or dimethyl sulfoxide (DMSO) for 1 hour, followed by treated with or without 5 µM indirubin for 72 hours. The Western blot assay results showed that colivelin significantly induced the phosphorylation of STAT3, while indirubin significantly inhibited it. Moreover, we found that pretreatment of colivelin could partly reverse the indirubin-induced suppression of STAT3 phosphorylation (Figure 5A). Next, flow cytometry assay showed that colivelin also reversed the cell apoptosis phenotype induced by indirubin (Figure 5B). In order to make our conclusion more solid, we repeated the treatment in OVCAR3 cells (Figure 5C). CCK-8 assay showed that cell viability inhibition induced by indirubin was significantly impaired by pretreatment of colivelin (Figure 5D). Overall, these results suggested that indirubin exerts anti-viability effects partly through the activation of STAT3 signaling pathway.

Figure 5 Colivelin could partly reverse the indirubin-induced suppression of cell proliferation and phosphorylation of Stat3.

Notes: (A) A2780 cells were pretreated with 0.5 µM colivelin (Stat3 activator) or DMSO for 1 hour and followed by treatment with or without 5 µM indirubin. Seventy-two hours later, the cells were harvested for Western blot assay. (B) A2780 cells were pretreated with 0.5 µM colivelin or DMSO for 1 hour and followed by treatment with or without 5 µM indirubin. Seventy-two hours later, the cells were harvested for flow cytometry analysis. (C) OVCAR3 cells were pretreated with 0.5 µM colivelin or DMSO for 1 hour and followed by treatment with or without 5 µM indirubin. Seventy-two hours later, the cells were harvested for Western blot assay. (D) OVCAR3 cells were exposed to 5 µM indirubin with or without 0.5 µM colivelin for 72 hours. Cell viability was measured by CCK-8 assays. The data are presented as mean ± SD. *P<0.05, **P<0.01, ***P<0.001 vs control group.
Abbreviation: NS, not significant.

Discussion

As an active component of the traditional Chinese herbal medicine, Danggui Longhui Wan, indirubin is known for treatment of chronic myelogenous leukemia.⁹ Besides, recent studies demonstrate that indirubin as well as its derivatives act as potent inhibitors against CDKs and display potent growth inhibitory effects in human cancer cells.^16,17 Specifically, indirubin inhibits the proliferation of a wide range of cancer cells, for example, lung cancer cell lines A549 and LXFL529L, breast cancer cell line MCF-7, prostate cancer cell line PC-12, and leukemic cell line K-562.^10,11,16,18 Among most of these cell lines, indirubin inhibited cells proliferation in a dose-dependent manner. Induction of cell apoptosis could also be caused by arresting of cell cycle in the G1/S or G2/M by indirubin.^10,17 It remains unclear if other mechanisms exist for explaining the apoptosis induction by indirubin.

Liu et al reported the anti-survival effect of MLS-2384 (a new 6-bromoindirubin derivative) on variant cancer cells, including ovarian cancers.¹⁹ Yu et al demonstrated an inhibitory effect of (2Z, 3E)-6-bromoindirubin-3′-oxime (a bromoindirubin derivative, known as “BIO”) on cell proliferation, cell cycle, migration, and invasion in ovarian cancer cells.²⁰ In the present study, we conducted experiments on 2 different ovarian cancer cell lines. Our results showed that simple indirubin significantly inhibited cell viability and induced apoptosis in ovarian cancer cells. Detailed mechanism studies revealed that indirubin repressed the expression of phosphorylated-STAT3, thus repressing the downstream pro-survival proteins and elevating pro-apoptosis ones. Mechanistic studies by using STAT3 activator showed that indirubin exerts anti-viability effects partly through activation of STAT3 signaling pathway.

As is known, signal transducer and activator of transcription (STAT) proteins play an important role in cancer cell survival.^21,22 Among the protein family members, STAT3 is often constitutively activated in many human cancer cells, and has been implicated as a promising target for cancer therapy.²¹ Its persistent signaling significantly contributes to oncogenesis by promoting cell proliferation and preventing apoptosis.²² STAT3 activates tumorigenesis through directly upregulating of genes encoding apoptosis inhibitors and cell cycle regulators like Bcl-xL, Cyclin D1, and C-myc.^21,22 The link between indirubin and STAT3 activation has also been discovered by several other groups previously.^23–25

Conclusion

Our study provided solid evidence for anti-survival activity of indirubin by inhibiting cell viability and inducing apoptosis in human ovarian cancer cells, which involved impaired STAT3 signaling. Therefore, indirubin is a potent inhibitor of the STAT3 signaling and can serve as a potential drug candidate against human ovarian cancer.

Disclosure

The authors report no conflicts of interest in this work.