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Signal transducer and activator of transcription 3 (STAT3) is activated in majority of ovarian tumors and confers resistance to cisplatin treatment in patients with ovarian cancer. We have reported previously that diindolylmethane (DIM) inhibits the growth of ovarian cancer cells. However, to date the exact mechanism by which DIM induces growth suppressive effects has not been clear. In this report the mode of action of DIM is investigated.
Six human ovarian cancer cell lines and an ovarian tumor xenograft animal model were used to study the effect of diindolylmethane alone or in combination with cisplatin.
Diindolylmethane treatment induced apoptosis in all six ovarian cancer cell lines. Phosphorylation of STAT3 at Tyr-705 and Ser-727 was reduced by DIM in a concentration-dependent manner. In addition, diindolylmethane treatment inhibited nuclear translocation, DNA binding, and transcriptional activity of STAT3. Interleukin (IL)-6-induced phosphorylation of STAT3 at Tyr-705 was significantly blocked by DIM. Overexpression of STAT3 by gene transfection blocked DIM-induced apoptosis. In addition, DIM treatment reduced the levels of IL-6 in ovarian cancer cells and in the tumors. DIM treatment also inhibited cell invasion and angiogenesis by suppressing hypoxia-inducible factor 1α (HIF-1α) and vascular epithelial growth factor (VEGF). Importantly, diindolylmethane treatment potentiated the effects of cisplatin in SKOV-3 cells by targeting STAT3. Oral administration of 3 mg diindolylmethane per day and subsequent administration of cisplatin substantially inhibited in vivo tumor growth. Western blotting analysis of tumor lysates indicated increased apoptosis and reduced STAT3 activation.
These findings provide a rationale for further clinical investigation of DIM alone or in combination for chemoprevention and/or chemotherapy of ovarian cancer.
Ovarian cancer continues to be a major worldwide gynecological malignancy. Approximately 25,000 new cases are diagnosed each year in the USA, and 15,000 patients die of this malignancy . Currently, no sufficiently accurate screening tests to diagnose this malignancy are available. Consequently, it is detected only in its late stages leading to minimal survival rates after diagnosis. At stage III, ovarian cancer metastasizes and spreads to the surrounding organs such as the peritoneum and stomach. By stage IV, ovarian cancer spreads to distant metastatic organs such as the lungs and liver. Cisplatin is a well established platinum drug used to treat various cancers, including ovarian cancer [2,3]. Patients treated with cisplatin often relapse or do not respond to the treatment. In addition, at higher doses cisplatin exerts side effects such as nephrotoxicity and ototoxicity in patients . Several reports suggest that signal transducer and activator of transcription 3 (STAT3) overexpression is positively associated with cisplatin resistance .
The STATs are a novel class of transcription factors that are positively associated with the growth and survival of cells . STAT3 is a receptor tyrosine kinase that is activated either by upstream receptor kinases such as Janus activated kinases (JAKs) or cytokines such as interleukin (IL)-6 . When IL-6 binds to its receptors, it activates STAT3 by phosphorylating it at Tyr-705. Activation of STAT3 at Tyr-705 leads to formation of a homodimer that translocates to the nucleus, where it binds to the promoter regions of several genes that transactivate STAT3-responsive genes such as Mcl-1, survivin and cyclin D1 [8-10]. It is also phosphorylated at Ser-727, which is not required for DNA binding activity but is important for its maximal transcriptional activity. STAT3 activates vascular endothelial growth factor (VEGF), thereby promoting neovascularization in tumors . It also regulates hypoxia-inducible factor 1α (HIF-1α) and vascular epithelial growth factor (VEGF) during hypoxia, leading to hypoxia-induced angiogenesis [12,13].
Previously published reports suggest that STAT3 is overexpressed in various tumors, including ovarian tumors . A recent clinical study scored 322 patients for overexpression of phosphorylated (p)-STAT3 and observed that 303 patients were positive for hyperactivation of STAT3, accounting for 94% of the study group . Furthermore, various reports indicate the role of STAT3 in resistance of ovarian cancer to chemotherapy . Since STAT3 is involved in various aspects of cancer growth ranging from tumor initiation, angiogenesis, and metastasis, it represents an attractive target for intervention.
3,3'-Diindolylmethane (DIM), an active metabolite of indole-3-carbinol, is present in cruciferous vegetables . Accumulating epidemiological evidence indicates an inverse relationship between intake of cruciferous vegetables and the risk of ovarian cancer . Several studies, including those from our laboratory, have suggested that DIM possesses chemopreventive and therapeutic properties [17-19]. Moreover, DIM was shown to be non-toxic to normal cells . A recently concluded DIM clinical trial demonstrated that 50% of cervical cancer patients showed improvement . It is also currently in clinical trials for prostate cancer . The effects of DIM were recently discussed in detail by Banerjee et al. . In our previous study, we showed that DIM exhibits antiproliferative properties in ovarian cancer cells by causing G2/M cell cycle arrest . However, the mechanism by which DIM inhibits proliferation of ovarian cancer cells was not clear.
In the present study, we provide evidence that DIM induces apoptosis in ovarian cancer cells by blocking the activation of STAT3 and its downstream effector molecules, while IL-6 treatment or overexpression of STAT3 significantly protects ovarian cancer cells from DIM-induced apoptosis. Our results also show that DIM suppresses angiogenesis and metastasis. In addition, DIM potentiates the effect of cisplatin in inducing apoptosis and inhibiting angiogenesis and metastasis. As a proof of concept, in vivo efficacy of DIM alone and in combination with cisplatin also was evaluated.
BR-DIM was a kind gift from Dr Michael Zeligs (Bio Response, Boulder, CO, USA). Cisplatin was obtained from Novaplus (Bedford, OH, USA). Antibodies against cleaved (Cl)-caspase 3, Cl-poly(ADP-ribose) polymerase (PARP), p-STAT3 (Tyr-705), STAT3, Mcl-1, and survivin were obtained from Cell Signaling Technology (Danvers, MA, USA). VEGF antibody was obtained from R&D systems (Minneapolis, MN, USA), Lamin B was from Santa Cruz Biotechnologies (Santa Cruz, CA, USA), and p-STAT3 (Ser-727) and HIF-1α were obtained from Abcam Inc. (Cambridge, MA, USA). Actin antibody, IL-6, MCDB105 and Medium 199 were procured from Sigma Aldrich (St Louis, MO, USA). RPMI and McCoy 5A were purchased from Mediatech (Manassas, VA, USA). NE-PER nuclear fractionation kit was from Thermo Scientific. EZ-TFA transcription factor assay kit was obtained from Upstate (Millipore, Billerica, MA, USA). Dual luciferase kit was bought from Promega (Madison, WI, USA). The VEGF Elisa kit was from Invitrogen (Carlsbad, CA, USA) and FuGENE 6 was obtained from Roche (South San Francisco, CA, USA). IL-6 secretion ELISA kit was from ebiosciences (San Diego, CA, USA).
SKOV-3, OVCAR-3 and TOV-21G cells lines were procured from American Type Culture Collection (ATCC; Manassas, VA, USA). SKOV-3 cells were maintained in McCoy's 5A medium supplemented with 10% fetal bovine serum (FBS). OVCAR-3 cells were maintained in RPMI medium supplemented with 20% FBS, 10 mM sodium pyruvate, 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), 10 mg/l bovine insulin and 4.5 g/l glucose. Human normal ovarian surface epithelium cells (NOSE) were a kind gift from Dr Jinsong Liu at MD Anderson, Houston, TX, USA. NOSE cells were previously transfected with the SV40 early region expressing large T and small t antigens as described elsewhere . NOSE and TOV21G cells were maintained in 1:1 mixture of MCDB105 and Medium 199 supplemented with 15% FBS. The A2780 cell line (a kind gift from Dr Thomas Hamilton, Fox Chase Cancer Center, Philadelphia, PA, USA) was maintained in RPMI media supplemented with 10% FBS and 2.7 units/ml insulin. OVCAR-429 and OVCAR-433 (a kind gift from Dr Laurie Hudson, University of New Mexico) were maintained in Dulbecco's modified Eagle medium (DMEM) with 10% FBS. A 1% antibiotic mixture was used in all the above media. All the cell lines were maintained at 37°C in a humidified incubator circulated with 5% CO2/95% air. The cell survival assay was performed as described by our group previously .
SKOV-3 cells were plated at a density of 0.3 × 106 cells per well in a six-well plate and allowed to attach overnight. Cells were then treated with or without DIM. After 24 h cells were exposed to IL-6 for 15 minutes, washed, suspended in binding buffer, and incubated for 15 minutes with annexin V-FITC (BD Biosciences, San Jose, CA, USA). Fluorescence was measured using a C6 Accuri flow cytometer (Ann Arbor, MI, USA) with a minimum of 10,000 events per sample as previously described by our group .
SKOV-3, OVCAR-3, TOV-21G and A2780 cells were exposed to varying concentrations of DIM alone or in combination with cisplatin. Cells were collected, lysed, and about 20 to 80 μg protein was subjected to SDS gel electrophoresis followed by immunoblotting as previously described by our group .
SKOV-3, OVCAR-3, TOV-21G, or A2780 cells were plated at a density of 1 × 106 in 100 mm culture dishes and exposed to different concentrations of DIM for 24 h. Nuclear fraction was extracted using NE-PER kit from Thermo Scientific according to the manufacturer's instructions.
DNA binding activity of STAT3 was measured by Universal EZ-TFA transcription factor assay colorimetric kit. SKOV-3 or OVCAR-3 cells were treated with or without DIM for 24 h. Nuclear extracts were used to determine the specific STAT3 DNA binding activity as previously described by our group .
Transcriptional activity of STAT3 was determined in SKOV-3 and OVCAR-3 cells by transfecting the cells with 2 μg pLuc-TK/STAT3, which encoded firefly luciferase under the control of STAT3 promoter, and with 0.2 μg of a pRL-TK, which constitutively expressed Renilla luciferase, the latter as a transfection efficiency control. At 24 h after transfection, cells were treated with or without DIM for 24 h. Whole cell lysates were collected using passive lysis buffer provided by dual luciferase reporter assay kit. Renilla and firefly luciferase activities were measured by a luminometer. Firefly luciferase activities were corrected for Renilla values and then normalized relative to dimethylsulfoxide (DMSO) control as previously described .
SKOV-3, OVCAR-3, or TOV-21G cells were treated with 75 μM DIM for 24 h followed by incubation with 10 ng/ml IL-6 for 15 minutes. Cells were then processed for apoptosis assay or western blotting as described above.
Since HIF-1α is proteasomally degraded, SKOV-3 and OVCAR-3 cells were pretreated with 10 μM MG132 for 1 h and then treated with 75 μM DIM for 6 h. In another experiment, after DIM treatment, cells were treated with or without 10 ng/ml IL-6 for 15 minutes. Samples were processed for western blotting as described above.
A total of 0.3 × 106 SKOV-3 cells were plated in McCoy's 5A medium containing 10% FBS without antibiotics and allowed to attach overnight. Complexes were prepared by incubating 2 μg STAT3α plasmid with 6 μl FuGENE 6 transfection reagent in 100 μl McCoy media without serum or antibiotic for 1 h. These complexes were then added to the cells. At 6 h after transfection, the media was replaced by regular media. After 24 h of transfection, cells were further treated with or without DIM for 24 h.
A total of 0.3 × 106 SKOV-3 cells were plated in McCoy's 5A medium containing 10% FBS without antibiotics and allowed to attach overnight. Complexes were prepared by incubating 2 μg STAT3 shRNA with 6 μl FuGENE 6 transfection reagent in 100 μl McCoy media without serum or antibiotic for 1 h. These complexes were then added to the cells. At 6 h after transfection, media was replaced by regular media. After 24 h of transfection, cells were processed for apoptosis assay as described above.
About 10,000 SKOV-3, OVCAR-3 or OVCAR-429 cells were plated per well in a 96-well plate. Cells were starved overnight followed by treatment with DIM for 24 h. After 24 h, medium was collected and processed for measuring secreted IL-6 levels using ELISA kit according to manufacturer's instructions.
Aortic ring spouting assay was performed as previously described . In brief, 1 mm long rings were excised from rat thoracic aorta. The rings were submerged in 350 μL Matrigel (BD Biosciences) containing 50 ng/ml IL-6. After a 24-h incubation, DIM, cisplatin, or both were added to the rings and incubated for an additional 3 to 5 days. The aortic rings that formed microvascular-like sprouts were photographed under light microscope (Olympus Inc., PA, USA) and the results were quantified by ImageJ V.1.43 software provided by NIH.
Secreted VEGF levels in DIM treated SKOV-3 and OVCAR-3 cell culture medium were measured using ELISA kit according to manufacturer's instructions.
Wound healing assay was performed as described previously . Confluent monolayers of SKOV-3; OVCAR-3; and TOV-21G cells in six well plates were scratched with a 1 ml pipette tip and incubated in respective medium containing 50 μM DIM. Cells were photographed under a light microscope (Olympus) at 0, 24 and 48 h and the results were quantified by ImageJ software (NIH).
Cell invasion was performed according to the manufacturer's instructions in transwell Boyden's chambers with 8.0 μm pore size filters (BD Biosciences). Briefly, cells were serum starved overnight and harvested by trypsinization. A suspension of 20,000 SKOV-3 cells in 600 μL McCoy medium containing 1% serum were seeded on the upper well of the Boyden's chamber and the lower chamber was filled with 1.5 ml of media containing 1% serum. After incubation for 2 h, DIM or cisplatin or both were added to the upper chamber whereas 10% FBS and 20 ng/ml VEGF was added to the lower chamber as chemoattractant. After incubation for 24 h, cells from the upper chamber were removed by wiping with a cotton swab, and the filter was fixed with 10% trichloroacetic acid (TCA) and stained with 0.4% (w/v) sulforhodamine B (SRB) solution. The filters containing stained cells were removed from the transwell chambers and individually transferred to individual wells in a 96-well plate. The SRB dye retained on the filter was extracted with 10 mM Tris buffer and the absorbance was measured at 570 nm using a microplate reader (BioTek Instruments, VT, USA). Assays were performed in duplicates and data was expressed as percent migration with control.
Female athymic nude mice, 4 to 6 weeks old, were purchased from Charles River Laboratories (Wilmington, MA, USA). The use of mice and their treatment was approved by Institutional Animal Care and Use Committee (IACUC), Texas Tech University Health Sciences Center, and all the experiments were carried out in strict compliance with regulations. Mice were fed with antioxidant-free AIN-76A special diet for a week before starting the experiment. About 5 × 106 SKOV-3 cells were injected subcutaneously into both right and left flanks. Eight mice were assigned randomly to each group. Since each mouse was implanted two xenografts, each group had 16 tumors. Once each mouse achieved a tumor of about 90 mm3, the control group received PBS whereas mice in the treatment group received 3 mg DIM suspended in PBS by oral gavage every day. At day 34, 5 mg/kg cisplatin was injected intraperitoneally to the treatment group mice. Beginning on the 7th day after cell implantation, tumor volume was measured three times a week using vernier calipers until day 48, as previously described by our group . On day 48 the mice were killed and tumors were removed for western blot analysis.
Around 5,000 cells in 0.1 ml medium were plated per well in 96 well plates and allowed to attach overnight. Desired concentrations of DIM were added to the cells and incubated at 37°C for 24 h. The cells were then processed and stained with 0.4% SRB solution and the absorbance was read at 570 nm using a Biotek plate reader as described by our group previously .
All the statistical analyses were performed using Prism 5.0 (GraphPad Software Inc., San Diego, CA, USA). The data represents mean values with SD. The Student's t test was used to compare the control and treated groups. In experiments involving more than three groups, non-parametric analysis of variance followed by Bonferroni post hoc multiple comparison test was used. All statistical tests were two sided. Differences were considered statistically significant when the P value was less than 0.05.
We previously reported that DIM inhibits the growth of ovarian cancer cells by causing cell cycle arrest ; however, the exact mechanism was not clear. The apoptosis-inducing effect of DIM was determined in ovarian cancer cells using annexin V-FITC. Treatment of SKOV-3 cells with 50 μM or 75 μM DIM for 24 h resulted in an approximately 2.8-fold to 5.2-fold increase in apoptosis (Figure (Figure1A).1A). To rule out the cell specific effects of DIM, we evaluated DIM-induced apoptosis in five other ovarian cancer cell lines. Our results showed that apoptosis induced by DIM was nearly 3.6-fold to 5.2-fold higher in OVCAR-3, 4.9-fold to 7.1-fold higher in TOV-21G, 10.1-fold to 11.8-fold higher in A2780, fourfold to fivefold higher in OVCAR-429 and threefold to fourfold higher in OVCAR-433 cells (Figure (Figure1A).1A). Apoptosis-inducing effects of DIM were further confirmed by western blot analysis that revealed the cleavage of caspase 3 and PARP in DIM-treated ovarian cancer cells (Figure (Figure1B).1B). These results clearly establish that DIM induces apoptosis in ovarian cancer cells.
Our next step was to investigate the mechanism by which DIM induces apoptosis. STAT3 is activated in almost 90% of ovarian cancers. Overexpression of STAT3 was reported in stage III and IV ovarian tumors . We hypothesized that DIM induces apoptosis in ovarian cancer cells by inhibiting STAT3, and then systematically tested our hypothesis. SKOV-3, OVCAR-3, TOV-21G, A2780, OVCAR-429 and OVCAR-433 cells treated with varying concentrations of DIM were subjected to western blotting. Our results clearly show that DIM substantially inhibits the activation of STAT3 by suppressing phosphorylation at Tyr-705 and Ser-727 (Figure 2A i-vi). The protein levels of STAT3 decreased modestly with DIM treatment. Our results further show that the expression of Mcl-1 and survivin were drastically decreased by DIM treatment in a concentration-dependent manner in all four cell lines (Figure 2A i-iv). Regulated by STAT3, both Mcl-1 and survivin have been implicated in cancer growth. These results demonstrate that DIM targets STAT3 pathway in ovarian cancer cells.
Once phosphorylated at Tyr-705, STAT3 forms a homodimer and translocates into the nucleus where it gets involved in the transcription of cell survival genes such as Mcl-1, survivin. Our results show that nuclear translocation of STAT3 was blocked by DIM treatment in SKOV-3, OVCAR-3, TOV-21G and A2780 cells (Figure 2B i-iv) and strengthen our hypothesis that DIM inhibits the growth of ovarian cancer cells by blocking STAT3.
Upon translocating to the nucleus, STAT3 binds to specific response elements in the promoter regions of its responsive genes. Since we observed that DIM blocked the nuclear translocation of STAT3, our next step was to determine whether DIM can inhibit DNA binding and transcriptional activity of STAT3. DNA-binding activity of STAT3 was determined by Universal EZ-TFA transcription factor colorimetric assay using the nuclear lysates of cells treated with or without DIM. Our results show that DIM treatment resulted in approximately 60% inhibition of DNA binding activity in SKOV-3 cells (Figure 2C i). Around 30% inhibition of DNA binding activity was observed in OVCAR-3 cells by DIM (Figure 2C ii).
We then evaluated the transcriptional activity of STAT3 by luciferase assay. We observed a dramatic reduction in STAT3 transcriptional activity by DIM treatment. In SKOV-3 and OVCAR-3 cells, transcriptional activity was reduced by 80% (Figure 2D i, ii). Similarly, in TOV21G and A2780 cells, transcriptional activity decreased by 90% (Figure 2D iii, iv).
STAT3 can be activated by IL-6, a cytokine that binds to its receptor and phosphorylates at Tyr-705. Exposing SKOV-3 or OVCAR-3 cells to 10 ng/ml IL-6 for 15 minutes led to an enormous activation of STAT3 (Figure 3A,B). However, IL-6 treatment failed to induce a significant activation of STAT3 in DIM treated cells (Figure 3A i, B i, C). STAT3 protein level was not affected by IL-6 treatment (Figure 3A i). We further observed that IL-6 treatment significantly blocked DIM-induced cleavage of caspase 3 and PARP (Figure (Figure3A).3A). These results were confirmed by annexin staining showing that IL-6 significantly blocked DIM-induced apoptosis (Figure 3A ii). Similarly, in OVCAR-3 cells, apoptosis induced by DIM was significantly blocked by IL-6 (Figure 3B ii).
To further strengthen our observation that DIM-induced apoptosis was mediated by STAT3 inhibition in ovarian cancer cells, we transiently transfected SKOV-3 cells with STAT3 encoding plasmid for 24 h, resulting in an almost twofold increase in the expression of STAT3 (Figure 3E i). Correspondingly, phosphorylation of STAT3 at both Tyr-705 and Ser-727 also increased substantially. STAT3 overexpression completely protected SKOV-3 cells from DIM-induced apoptosis as evaluated by cleavage of caspase 3 and PARP (Figure 3E i). These observations were further confirmed by annexin V apoptosis assay by flow cytometry (Figure 3E ii). Taken together, our results clearly indicate that apoptosis induced by DIM was almost completely blocked in the cells overexpressing STAT3 (Figure 3D ii), establishing STAT3 as a target of DIM in ovarian cancer cells.
To address whether or not inhibition of STAT3 induces apoptosis in ovarian cancer cells, we silenced STAT3 using shRNA in SKOV-3 cells. Supporting our hypothesis, our results show that silencing STAT3 resulted in about 35% apoptosis in SKOV-3 cells suggesting the critical role of STAT3 in ovarian cancer cells (Figure (Figure3D).3D). Our results are in agreement with a previously published study that showed that STAT3 specific inhibitor (AG490) induced apoptosis in ovarian cancer cells .
IL-6, a cytokine, activates STAT3 by phosphorylating it at Tyr-705. High levels of circulating IL-6 were observed in ovarian cancer patients . Since we observed that DIM can suppress IL-6-induced activation of STAT3 in ovarian cancer cells, we hypothesized that DIM mediated inhibition of STAT3 is in fact by inhibition of IL-6. We therefore measured IL-6 secretion by ovarian cancer cells using a commercial ELISA kit. Our results demonstrate that DIM drastically blocks the secretion of IL-6 in SKOV-3, OVCAR-3 and OVCAR-429 cells (Figure 3F i-iii). Reduction in IL-6 secretion levels ranged from 60% to 80% in three different cell lines.
Recent literature suggested a novel role of STAT3 in angiogenesis and metastasis. Since DIM suppressed the activation of STAT3 in ovarian cancer cells, we wanted to test whether DIM can inhibit invasion and angiogenesis. We first determined the anti-invasive potential of DIM by evaluating cell migration in a wound healing assay. A wound was made on confluent monolayer cells with a pipette tip and, after washing with fresh medium, cells were treated with or without 50 μM DIM. Our results revealed that after 24 h DIM treatment, SKOV-3 cells migrated into 20% of the wounded area, whereas control cells migrated into 80% of the wounded area, showing the potential anti-invasive property of DIM (Figure (Figure4A).4A). Similar observations were made in OVCAR-3 and TOV-21G cells (Figure 4B, C).
Since several studies have established the role of activated STAT3 in tumor angiogenesis, we next sought to determine the antiangiogenic potential of DIM. We used an aortic ring model where microvessel sprouting occurs in response to growth stimulatory signals. Treatment with IL-6 induced a massive microvessel formation on rat aortic rings after 24 h of incubation. However, microvessel sprouting was drastically reduced in aortic rings treated with DIM (Figure (Figure4D4D).
STAT3 positively regulates HIF-1α and VEGF under hypoxia. VEGF has also been shown to be regulated by STAT3 in an HIF-1α-dependent manner . Under normal conditions, HIF-1α is constitutively synthesized and subjected to proteasomal degradation to maintain minimal levels. In order to determine the effect of DIM on HIF-1α expression, cells were treated with MG132, a known proteasomal inhibitor, in the presence or absence of DIM. Our results show that HIF-1α expression was drastically increased after 6 h of MG132 treatment. However, treatment of SKOV-3 or OVCAR-3 cells with DIM after MG132 treatment did not result in the accumulation of HIF-1α (Figure (Figure4E).4E). These results indicate that DIM suppresses HIF-1α induction (Figure (Figure4E).4E). To delineate the role of STAT3 in DIM-mediated HIF-1α down regulation, cells were treated with IL-6, which activates STAT3 phosphorylation, leading to the induction of HIF-1α. Our results further show that IL-6-induced HIF-1α expression was significantly attenuated by DIM (Figure (Figure4F).4F). VEGF expression, which normally is regulated by HIF-1α, was also substantially reduced by DIM treatment (Figure (Figure4F).4F). These results provide critical evidence that DIM inhibits angiogenesis in ovarian cancer cells by downregulating HIF-1α and VEGF through STAT3.
We wanted to determine whether DIM can potentiate the effect of cisplatin, a drug used to treat ovarian cancer patients. Cisplatin usually is associated with several side effects such as renal toxicity and reduction of white and red blood cells. Moreover, tumors often become resistant to cisplatin therapy. Hence, enhancing the effect of cisplatin at low doses by agents that are non-toxic may be a better strategy, not only for effective treatment but also to reduce harmful side effects. To test whether or not DIM potentiates the effect of cisplatin, SKOV-3 cells were treated with 20 μM or 50 μM DIM for 24 h followed by exposure to 10 μM cisplatin for an additional 24 h. It is important to mention that the IC50 of cisplatin in SKOV-3 cells is 40 μM; we used one-quarter of the IC50 concentration. Growth inhibition in combination treatment was significantly higher as compared to either treatment alone (Figure (Figure5A).5A). We observed around 50% to 70% reduction in the survival of SKOV-3 cells treated with a combination of DIM and cisplatin as compared to 28% by cisplatin alone (P < 0.001). We calculated the combination index (CI) for DIM and cisplatin combination treatment in SKOV-3 cells. CI values for the combination of cisplatin with 20 μM and 50 μM DIM treatment were 0.45 and 0.56, respectively, indicating the synergistic effect of DIM with cisplatin.
We next wanted to identify the mechanism behind the synergistic effects of DIM with cisplatin. We hypothesized that the enhanced effect of cisplatin by DIM was due to modulation of STAT3 pathway. In agreement with our hypothesis, combination treatment strongly suppressed the activation of STAT3 at Tyr-705 or Ser-727 as compared to cisplatin only treatment (Figure (Figure5B).5B). Mcl-1 also was downregulated in a similar manner. It is important to note that survivin, which is a positive regulator of growth and a major downstream target of STAT3, was drastically upregulated by cisplatin treatment alone. Nonetheless, DIM completely blocked cisplatin-mediated upregulation of survivin in the combination treatment (Figure (Figure5B).5B). Increased cleavage of caspase 3 and PARP by combination treatment indicated significantly more apoptosis as compared to either treatment alone. Furthermore, combination treatment completely abolished the phosphorylation and reduced the expression of STAT3 in the nuclear fraction of cells (Figure (Figure5C).5C). Similarly, transcriptional activity of STAT3 was also significantly suppressed by combination treatment (Figure (Figure5D5D).
We then wanted to know if combination treatment could inhibit angiogenesis in a rat aorta model. Our data showed that after 72 h, microvessel sprouting in rat aorta was not suppressed by cisplatin treatment (Figure (Figure5E).5E). However, combination treatment completely blocked microvessel sprouting (Figure (Figure5E).5E). The combination treatment of DIM with cisplatin also significantly blocked the invasion of the cells as evaluated by the Boyden's chamber technique (Figure (Figure5F).5F). However, cisplatin alone had hardly any inhibitory effect on the invasion of cells (Figure (Figure5F).5F). We also tested whether DIM alone or in combination inhibited VEGF secretion. Our results clearly demonstrate that DIM treatment in combination with cisplatin decreased the VEGF secretion by 60% as compared to control or cisplatin treatment only in both SKOV-3 and OVCAR-3 cells (Figure (Figure5G5G).
We demonstrated that DIM induces apoptosis in ovarian cancer cells and enhances the effect of cisplatin by inhibiting STAT3 pathway in culture models. To validate these effects in vivo, we performed a tumor xenograft assay. About 5 × 106 SKOV-3 cells were injected subcutaneously into both the right and left flanks of female athymic nude mice. Once each mouse had a tumor of about 90 mm3, they were randomized into four groups. DIM treatment started 24 days after tumor implantation, and cisplatin treatment began 10 days later. Our results demonstrated that DIM alone and in combination treatment substantially retarded the growth of SKOV-3 tumors as compared to control or cisplatin treatment. For example, at day 48 the average tumor volume in control mice and cisplatin-treated mice was around 400 mm3 and 300 mm3, respectively, whereas the average tumor volume in mice that received DIM alone or in combination with cisplatin was 210 mm3 and 138 mm3, respectively (Figure (Figure6A).6A). The combination treatment suppressed tumors by 65% as compared to controls. Interestingly, there was no significant change in the weight of mice treated with DIM as compared to mice in the control group. The weight of mice declined significantly in response to cisplatin treatment. However, the decline in weight in the combination treatment group was not as significant as in the mice receiving cisplatin treatment alone (Figure 6A ii). To determine whether DIM-mediated tumor growth suppression was due to inhibition of STAT3, tumor lysates were subjected to western blotting. As shown in Figure Figure6B,6B, p-STAT3 (Tyr-705), STAT3, and Mcl-1 were downregulated in the tumors of mice treated with DIM alone or in combination with cisplatin as compared to control or cisplatin treatment. Furthermore, cleavage of caspase 3 and PARP increased significantly in the tumors of mice treated with combination, yet again confirming that DIM suppressed tumor growth by inducing apoptosis in vivo. Furthermore, IL-6 levels in tumor lysates from DIM treated mice were significantly less as compared to levels in the tumor lysates from control mice (Figure (Figure6D).6D). Taken together, our results clearly establish that DIM induces apoptosis in ovarian cancer cells in vitro and in vivo by targeting the STAT3 pathway and synergistically enhancing the effects of cisplatin.
In order to determine whether DIM is toxic to normal ovarian cells, we treated NOSE cells with various concentrations of DIM for 24 h. Interestingly, our results showed that DIM treatment caused minimal reduction in the survival of non-tumorigenic ovarian cells (Figure (Figure7A).7A). At a concentration as high as 120 μM, DIM reduced the survival of NOSE cells by about 25%, whereas a 75% reduction in survival was observed in TOV-21G ovarian cancer cells (Figure (Figure7A).7A). These results indicate that DIM is minimally toxic to normal ovarian surface epithelial cells.
To gain further insight into the effect of DIM on p-STAT3, NOSE cells were treated with varying concentrations of DIM for 24 h. Surprisingly, we observed phosphorylation of STAT3 in these cells and 75 μM DIM significantly reduced STAT3 phosphorylation (Figure (Figure7B).7B). Although STAT3 is mainly known to be activated and/or overexpressed in tumorigenic cells, a few recent studies have suggested that IL-6 and STAT3 are activated at low levels in normal ovaries [14,32]. However, the exact mechanism and role of activated STAT3 in normal ovaries is not clear. Our results clearly show that STAT3 is a target of DIM.
Our results demonstrate that DIM suppresses the growth of ovarian cancer cells and potentiates the effect of cisplatin in vitro and in vivo by targeting STAT3 signaling without being toxic to normal ovarian cells. To the best of our knowledge, this is the first report demonstrating STAT3 as a target of DIM. Accumulated evidence indicates the involvement of STAT3 in the transformation of normal cells into malignant ones [30,33]. STAT3 is overexpressed in ovarian tumors and is associated with ovarian tumorigenesis . A recent study demonstrated that STAT3 is activated in 94% of ovarian cancer patients . Furthermore, STAT3 is also implicated in resistance to chemotherapy in ovarian cancer . Our studies showed that DIM-induced apoptosis in various ovarian cancer cells was mediated by substantially suppressing the phosphorylation of STAT3 at Tyr-705 and Ser-727. Tyrosine phosphorylation is mainly associated with oncogenic status of STAT3. The effects of DIM were not specific to only SKOV-3 cells as similar observations were made in various other ovarian cancer cell lines such as OVCAR-3, TOV-21G, A2780, OVCAR-429 and OVCAR-433. These studies agree with previous reports that demonstrate that inhibiting constitutive activation of STAT3 by STAT3 inhibitor AG490 inhibits tumor growth .
Unphosphorylated STAT3 resides in the cytoplasm and is activated by phosphorylation. Once phosphorylated at Tyr-705, STAT3 dimerizes and translocates into the nucleus [35,36]. Around 86% of ovarian tumor tissues have activated STAT3 in the nucleus and not in the cytoplasm . Our results clearly show that the nuclear translocation and activation of STAT3 was substantially reduced by DIM treatment. Inhibition of nuclear translocation in turn inhibits DNA binding activity and transcriptional activity of STAT3 [37,38]. Specific DNA binding of STAT3 leads to transcriptional activation of several downstream molecules such as survivin and Mcl-1. These results demonstrate that DIM treatment blocks the transcriptional and DNA binding activity of STAT3 and downregulates the expression of survivin and Mcl-1. Our observations confirm previous studies indicating that STAT3 inhibition downregulates survivin or Mcl-1 in various cancers [27,39,40]. It is noteworthy that a gene expression profiling of a previous study showed that survivin is a target of DIM . Survivin overexpression is implicated in resistance to cisplatin-induced apoptosis [42,43]. Our results showed that survivin expression was substantially upregulated by cisplatin treatment in ovarian cancer cells. However, DIM treatment completely abolished the overexpression of survivin by cisplatin, suggesting a potential role of DIM in reducing cisplatin-mediated resistance.
Various cytokines and growth factors can activate STAT3. IL-6 is well known to activate STAT3 by phosphorylation at Tyr-705. DIM not only eliminated constitutive activation of STAT3, but also blocked IL-6 mediated activation of STAT3. In addition, to convincingly establish STAT3 as a target of DIM, cells were transfected with STAT3 expression plasmid to activate STAT3 in ovarian cancer cells. Induction of apoptosis by DIM was almost completely blocked in cells overexpressing IL-6 or STAT3, demonstrating that induction of apoptosis in our model was mediated through STAT3 downregulation. Our data indicating that DIM induces apoptosis by inhibiting STAT3 was also supported by our STAT3 knockout studies, which demonstrated the induction of apoptosis when STAT3 was knocked out by shRNA. These results agree with a previous study showing the role of STAT3 in suppressing apoptosis in pancreatic cancer cells . Furthermore, DIM treatment dramatically reduced the secretion of IL-6 not only in ovarian cancer cells but also in tumors. Interestingly, a recent study reported higher IL-6 levels in ovarian cancer patients . This study indicated the IL-6-STAT3-HIF axis as an important target for therapy in ovarian cancer . Our results show that DIM treatment alone or in combination with cisplatin inhibited neovascularization induced by IL-6, suggesting the antiangiogenic potential of DIM. HIF-1α and VEGF play an important role in angiogenesis. HIF-1α is short lived and degrades proteasomally; however, MG132 blocks the degradation of HIF-1α. Our results show that HIF-1α expression retained by MG132 was suppressed as early as 6 h after DIM treatment. IL-6 also activated HIF-1α, which clearly indicates that HIF-1α perhaps is regulated through STAT3 in ovarian cancer cells. It is obvious that inhibition of HIF-1α by DIM was mediated through STAT3 in our model [13,44]. VEGF is another important regulator of angiogenesis and its expression in cancer cells has been shown to correlate with activation of STAT3 . Previous reports have suggested that overexpression of STAT3 increases VEGF expression, leading to angiogenesis . Hence disrupting the activation of STAT3 would inhibit VEGF, blocking angiogenesis . Our results demonstrated that DIM inhibits both VEGF expression and VEGF secretion. This explains the mechanism of the antiangiogenic effects of DIM in ovarian cancer cells in our study.
Cisplatin is a frontline drug used in the treatment of advanced ovarian cancer . Nonetheless, only 15% of patients treated with cisplatin achieve long-term survival; the rest experience persistent or recurrent disease . Moreover, cisplatin is associated with cytotoxicity and resistance to chemotherapy [48,49]. STAT3 activation or overexpression is associated with cisplatin resistance . Our results demonstrate that DIM potentiates the effect of cisplatin at one-quarter of its IC50 concentration by inhibiting the activation of STAT3. Combination treatment blocked phosphorylation of STAT3 at both Tyr-705 and Ser-727 when compared to cisplatin treatment alone. Likewise, VEGF secretion and angiogenic sprouting were noticeably reduced in combination treatment as compared to cisplatin alone. These results agree with previous studies that demonstrated inhibition of STAT3 by an analog of aspirin potentiated the effects of cisplatin . The CI provides qualitative information about the nature of drug interaction. CI values less than 1, equal to 1 or greater than 1 indicate synergistic, additive or antagonistic effects, respectively. Our CI values for the combination treatment at both the concentrations of DIM with cisplatin were less than 1, showing the synergistic effects of DIM with cisplatin.
Oral administration of 3 mg DIM per day substantially suppressed the growth of established ovarian tumors, indicating the tumor regression potential of DIM. However, complete regression of tumors was not observed with DIM. When given with cisplatin treatment, DIM further retarded the growth of tumors. The tumors from DIM or DIM plus cisplatin-treated mice clearly demonstrated inhibition of STAT3 signaling and increased apoptosis. Similar to our in vitro observations, cisplatin treatment caused a drastic increase in the expression of survivin in the tumors, which was completely suppressed by DIM in combination treatment. Interestingly, mice that received DIM did not show any significant change in body weight when compared with the weight of control mice. However, the mice that received cisplatin and DIM showed a decrease in weight, though this was not as drastic as in the mice that received only cisplatin, suggesting that DIM may reduce the systemic toxicity associated with cisplatin. DIM is a major indole compound present in cruciferous vegetables, and is consumed on a daily basis . A recent single dose phase I clinical trial suggested that 200 mg DIM is well tolerated not only by healthy volunteers but also in patients with cervical cancer [21,52]. In the same study 200 mg single dose produced a mean Cmax of 104 ng/ml and mean area under curve (AUC) of 553 h ng/ml. The half-life of this dose was 2.6 ± 0.7 h. Interestingly a single dose of DIM alone caused a significant clinical improvement in patients with stage II and stage III cervical intraepithelial neoplasia (CIN) . Administration of 2 mg/kg/day DIM via an oral route showed improvement in pap smear results, human papillomavirus (HPV) status, and improved CIN by 1 to 2 grades . Several pharmacokinetic studies on DIM have stated that up to 300 mg in a single dose of DIM can be tolerated by humans , indicating that our dose of DIM falls within the accepted and tolerated dose. Cisplatin in our studies was given intraperitoneally at a dose of 5 mg/kg twice a week, which is 14 mg/m2 when converted to the equivalent human dose . The weekly dose of cisplatin ranges from 40 to 140 mg/m2 in humans. We administered cisplatin twice a week, with an additive effect of 28 mg/m2, which is much lower than the regular dosage typically given to patients with cancer. If a low dose of cisplatin can be given to patients without the loss of any therapeutic effect but with reduced side effects, it would represent a significant breakthrough in clinical practice. Nevertheless, further clinical studies are needed to show that DIM can reduce the side effects of cisplatin.
In conclusion, our results firmly establish that DIM induces apoptosis in ovarian cancer cells by inhibiting STAT3 signaling. Our results also provide evidence that DIM inhibits the invasion of ovarian cancer cells and angiogenesis by inhibiting HIF-1α and VEGF, which are regulated by STAT3. Importantly, DIM potentiated the effect of cisplatin both in culture and in vivo by inhibiting STAT3. Taken together, the findings from our study provide support for the use of DIM alone or in combination with cisplatin in preclinical and clinical settings in the management of ovarian cancer patients.
For the first time, our study demonstrates that DIM targets STAT3 to suppress the growth of ovarian tumor cells in vitro and in vivo. Importantly, DIM inhibits angiogenesis and invasion of ovarian cancer cells. Our results also show that targeting STAT3 potentiates the effect of cisplatin both in culture as well as in a tumor xenograft model.
The authors declare that they have no competing interests.
Both PKK and SKS were responsible for designing the study, analyzing the data and writing the manuscript. Experiments were performed by PKK. Both authors read and approved the final manuscript.
The pre-publication history for this paper can be accessed here:
This work was supported in part by R01 grants CA106953 and CA129038 (to SKS) awarded by National Cancer Institute, NIH. We thank Dr Jacqueline Bromberg (Sloan Kettering Memorial Cancer Center, NY, USA) for providing STAT3α and STAT-Luc plasmids, Dr Thomas Hamilton (Fox Chase Cancer Center, PA, USA) for providing A2780 cells, Dr Jinsong Liu (MD Anderson, TX, USA) for providing NOSE cells, Dr Laurie Hudson (University of New Mexico, NM, USA) for providing OVCAR429 and OVCAR433 cells, and Dr Michael Zeligs (Bio Response, CO, USA) for providing BR-DIM for our studies. The technical help of Srinivas Reddy Boreddy and Kartick C Pramanik with the in vivo experiment is greatly appreciated.