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Resveratrol (RSV), a natural polyphenols, has been suggested to induce cell cycle arrest and activate apoptosis-mediated cell death in several cancer cells, including prostate cancer. However, several molecular mechanisms have been proposed on its chemopreventive action, the precise mechanisms by which RSV exerts its anti-proliferative effect in androgen-independent prostate cancer cells remain questionable. In the present study, we show that RSV activates autophagic cell death in PC3 and DU145 cells, which was dependent on stromal interaction molecule 1 (STIM1) expression. RSV treatment decreases STIM1 expression in a time dependent manner and attenuates STIM1 association with TRPC1 and Orai1. Furthermore, RSV treatment also decreases ER calcium storage and store operated calcium entry (SOCE), which induces endoplasmic reticulum (ER) stress thereby activating AMPK and inhibiting the AKT/mTOR pathway. Similarly, inhibition of SOCE by SKF-96365 decreases the survival and proliferation of PC3 and DU145 cells and inhibits AKT/mTOR pathway and induces autophagic cell death. Importantly, SOCE inhibition and subsequent autophagic cell death caused by RSV was reversed by STIM1 overexpression. STIM1 overexpression restored SOCE, prevent the loss of mTOR phosphorylation and decreased the expression of CHOP and LC3A in PC3 cells. Taken together, for the first time, our results revealed that RSV induces autophagy mediated cell death in PC3 and DU145 cells through regulation of SOCE mechanisms, including down regulating STIM1 expression and trigger ER stress by depleting ER calcium pool.
Prostate cancer (PCa) is the most commonly diagnosed cancer in the male population of western decent and is the leading cause of cancer related death in men who are older than 65 [1,2]. Anti-androgen therapy is remarkable in the early stages of prostate tumors development since the growth is completely dependent on androgens. However, in majority of cases, the tumor progress to androgen insensitive stage where androgen is not required for their growth, for which currently no successive therapy is available . Therefore, a better understanding of the mechanism(s) and identification of novel target molecules that control the androgen insensitive prostate cancer cell proliferation and the development of novel therapeutic drugs, are essentially needed in the near future.
Prostate epithelial cells express a large number of Ca2+ permeable channels that are required to regulate different cellular functions including proliferation and differentiation. Loss of Ca2+ homeostasis modulation, could be at least in part, the mechanisms where the prostate cancer epithelial cells become resistant to apoptotic stimuli which ultimately leads to uncontrolled proliferation and invasion [4,5]. Recent studies have suggested that intracellular Ca2+ as well as Ca2+ channels play a major role in PCa progression [6,7]. For example, double knockdown of alpha1D-adrenergic receptor (alpha1D-AR) and transient receptor potential vanilloid type 1 (TRPV1) inhibit noradrenalin induced PC3 cell proliferation by suppressing Ca2+ influx, and reducing the activation of phospholipase C (PLC), protein kinase C (PKC) and extracellular signal-regulated kinase 1/2 (ERK1/2) pathways . Similarly, other studies have shown that calcium influx through TRPC6, TRPV6, TRPM8 and T-type Ca2+ channels participate in the proliferation of prostate cancer cells [9-12]. On the other hand, massive Ca2+ influx via the store operated Ca2+ entry (SOCE) mechanism induces apoptosis mediated cell death in several cancer cells [5,13]. Therefore studying the Ca2+ permeable channels and its downstream signaling pathways may be effective in the identification of novel drug targets that could be used for tumor regression.
SOCE is an important cellular mechanism that ensure the optimal refilling of endoplasmic reticulum (ER) /sarcoplasmic reticulum (SR) Ca2+ stores, activation of several Ca2+ mediated pro and anti-survival mechanisms and gene transcription. In excitable and non-excitable cells, SOCE is mediated by store operated Ca2+ channels (SOCs) which are located in the plasma membrane and depletion of ER Ca2+ stores activates the SOCs mediated Ca2+ influx (known as SOCE). Interestingly, changes in ER Ca2+ levels and SOCs function play a crucial role in the establishment of an androgen independent apoptosis resistance phenotype of prostate cancer [5,14,15]. Members of TRPC family particularly, TRPC1 and TRPC4 have been identified as the promising molecular candidates for SOCs in androgen-dependent LNCaP cells [16,17] and notably, recent studies have identified two other molecular components of SOCs, Orai1 and STIM1 [18,19]. Stromal interaction molecule 1 (STIM1) is a single transmembrane ER/SR resident protein with NH2-terminal Ca2+ binding EF hand directed to the lumen of the ER that functions as a signal transducer from ER to SOCs. Upon store depletion, STIM1 translocates to plasma membrane where it interacts with TRPC1 and/or Orai1 to initiate SOCE . Several studies have shown that SOCE and SOCs are involved in cell cycle progression, proliferation and migration [9,20], but its role in prostate cancer as well as downstream signaling mechanism is still not yet established.
Dietary polyphenols are the most abundant natural antioxidants in the human food and recent reports suggested the efficacy of natural antioxidants in controlling the growth and migration of various cancers . Studies have suggested that dietary intake of natural antioxidants could halt cancer progression. Resveratrol (trans-3,4′ ,5-trihydroxystilbene; RSV), a natural polyphenolic antioxidant found in a wide variety of fruits including grapes, raspberries, and other plants. Several in vitro and in vivo studies have suggested the growth inhibitory efficacy of RSV in several types of cancer cells, notably leukemia, breast, colon, liver, lung, thyroid and other epithelial cancers [21,22]. Importantly, the anti-carcinogenic effect of RSV in prostate cancer has been shown and it’s widely associated with changes in the expression of cell cycle regulating molecules such as, cyclin A, cyclin E, cdc2 and Rb. Several other studies have also noticed that RSV inhibits the proliferation of androgen dependent and independent prostate cancer cell lines by activating the apoptotic pathway [23,24]. Moreover, RSV regulates the expression of PSA (prostate specific antigen) by an androgen receptor (AR) dependent and AR-independent mechanism, and also RSV enhances the effect of anti-AR drug bicalutamide [23-25]. However, the role of SOCE in RSV mediated anti-cancer effect and the precise mechanisms by which RSV exerts its anti-proliferative effect in androgen-independent prostate cancer cell lines remain unanswered. Thus, we have investigated whether SOCE is involved in prostate cancer cell proliferation and does RSV affects cell viability through SOCs dependent Ca2+ pathways. To address this, we have used two androgen-independent prostate epithelial cells PC3 and DU145 along with control RWPE-1 cells. The results from our study suggest that RSV inhibits prostate cancer proliferation by downregulating STIM1 thereby inhibiting SOCE and initiating autophagic cell death.
Control prostate cell line RWPE1 (CRL 11609) and prostate cancer cell line DU145 (HTB-81) and PC3 (CRL1435) cells were obtained from the American Type Culture Collection (Manassas, VA). Cells were cultured in their respective medium along with various supplements as suggested by ATCC. Cells were maintained at 37°C with 95% humidified air and 5% CO2 and were passaged as needed. Culture medium was changed twice weekly and cells were maintained in complete media, until reaching 90% confluence. For overexpression HA-STIM1 was used and 5 ug of plasmid DNA was transfected using Lipofectamine 2000 in Opti-MEM medium as per supplier’s instructions and assayed after 24 hours.
The ten thousand cells were plated in 96 well plate and synchronized by stimulating with 10% FBS. Then pulsed with BrdU for 2 h before BrdU incorporation was measured as per manufacturer’s instructions (Roche). For viability assays, cells were seeded on 96-well plates at a density of 0.5×105 cells/well. Cell viability was measured by using the Vybrant MTT cell proliferation assay kit (Molecular Probes, Invitrogen). Absorbance was read at 570 nm (630 nm as a reference) on a microplate reader (Molecular Devices). Cell viability was expressed as a percentage of the control culture.
Immunoprecipitation and Western blotting. Immunoprecipitations were carried out as described earlier . RIPA buffer was used to prepare the total cell lysates. Following stimulation, cells were lysed with RIPA buffer and used for immunoprecipitation. Protein concentrations were determined using the Bradford reagent (Bio-Rad) and and 25-50 ug of proteins were resolved in 4%–12% NuPAGE gels, followed by Western blotting with the desired antibodies. Crude membrane was prepared from DU145 and PC3 cells as described previously . Proteins were resolved on 4-12% Bis-Tris gels (Invitrogen), transferred to PVDF membranes and probed with respective antibodies. Peroxidase conjugated respective secondary antibodies were used to label the proteins. The proteins were detected by enhanced chemiluminescence detection kit (SuperSignal West Pico; Pierce). Antibodies that were used in this study are from Cell Signaling Technology (Danvers, MA) and Alomone Labs (TRPC1 and Orai1 antibodies). All other reagents used were of molecular biology grade obtained from Sigma chemicals unless mentioned otherwise.
PC3 and DU145 cells were transiently transfected with GFP-LC3 by using Lipofectamine 2000 in Opti-MEM medium as described by the manufacturer. After 24 h, cells were treated with RSV for 24h and then fixed in 4% formaldehyde for 10 min. Cells were then washed thrice with PBS and images were collected using a MRC1024-krypton/argon laser scanning confocal equipped with a Zeiss LSM 510 Meta photomicroscope.
Cells were incubated with 2 μM fura-2 (Molecular Probes) for 45 min, washed twice with Ca2+ free SES (Standard External Solution, include: 10 mM HEPES, 120 mM NaCl, 5.4 mM KCl, 1 mM MgCl2, 10 mM glucose, pH 7.4) buffer. For fluorescence measurements, the fluorescence intensity of Fura-2-loaded control cells was monitored with a CCD camera-based imaging system (Compix) mounted on an Olympus XL70 inverted microscope equipped with an Olympus 40× (1.3 NA) objective. A monochrometer dual wavelength enabled alternative excitation at 340 and 380 nm, whereas the emission fluorescence was monitored at 510 nm with an Okra Imaging camera (Hamamatsu, Japan). The images of multiple cells collected at each excitation wavelength were processed using the C imaging, PCI software (Compix Inc., Cranbery, PA), to provide ratios of Fura-2 fluorescence from excitation at 340 nm to that from excitation at 380 nm (F340/F380). Fluorescence traces shown represent [Ca2+]i values that are averages from at least 30-40 cells and are a representative of results obtained in at least 3-4 individual experiments.
For patch clamp experiments, coverslips with cells were transferred to the recording chamber and perfused with an external Ringer’s solution of the following composition (mM): NaCl, 145; CsCl, 5; MgCl2, 1; CaCl2, 1; Hepes, 10; Glucose, 10; pH 7.3 (NaOH). Whole cell currents were recorded using an Axopatch 200B (Axon Instruments, Inc.). The patch pipette had resistances between 3 −5 M after filling with the standard intracellular solution that contained the following (mM): cesium methane sulfonate, 150; NaCl, 8; Hepes, 10; EGTA, 10; pH 7.2 (CsOH). With a holding potential 0mV, voltage ramps ranging from −100mV to +100mV and 100ms duration were delivered at 2s intervals after whole cell configuration was formed. Currents were recorded at 2 kHz and digitized at 5–8 kHz. pClamp 10.1 software was used for data acquisition and analysis. Basal leak were subtracted from the final currents and average currents are shown. All experiments were carried out under room temperature.
Data analysis was performed using Origin 7.0 (OriginLab). Statistical comparisons were made using Student’s t test (2-tailed). Experimental values are expressed as mean ± SEM. Differences in the mean values were considered to be significant at P < 0.05 or P<0.01 or P < 0.001.
Ca2+ not only function as a second messenger, but have also been shown to be critical for cell proliferation and migration . Importantly, increase in Ca2+ signaling have been shown to activate the immediate early genes that are responsible for inducing resting cells to re-enter the cell cycle and has been suggested to be a target for anticancer therapy [28,29]. We thus evaluated the role of increasing Ca2+ concentration in prostate cancer cell proliferation and/or their survival. Importantly, increasing extracellular Ca2+ concentration showed a dose dependent increase in cell survival in prostate cancerous cells (DU145 and PC3) (Figure 1A and B). Although in the presence of increasing extracellular Ca2+ RWPE1 cells also showed a moderate increase in cell survival, the amount of increase in cell proliferation was relatively less when compared with cancer cells (data not shown). We next evaluated if cell proliferation was also increased under these conditions and again both DU145 and PC3 cells showed a significant increase in BrdU incorporation in the presence of increasing extracellular Ca2+ (Figure 1C and D). Overall, these data suggest that increasing extracellular Ca2+ is important for the increase of cell proliferation of prostate cancer cells.
Agonist-stimulated Ca2+ entry has been suggested to play an essential role in regulating cell survival and increasing cell proliferation. Importantly, in non-excitable cells both Orai1 and TRPC1 has been shown to be important for Ca2+ entry that are activated by agonist-mediated ER store depletion a phenomenon termed as SOCE. Thus, we next evaluated the expression of these Ca2+ entry channels in prostate cells. Although, no change in TRPC1 or Orai1 levels were observed in control and prostate cancer cells, a decrease in STIM1 levels was observed in control RWPE1 cells, when compared with prostate cancer cells (DU145 and PC3) (P<0.05; Figure 1E and F). STIM1 has been recently identified as a key Ca2+ entry regulator that is present in the ER and sense ER Ca2+ levels . Furthermore, upon store depletion STIM1 has been shown to interact with TRPC1 and Orai1 channels to initiate Ca2+ entry via SOCE that could be essential for cell proliferation and survival . Importantly, the functional interaction between STIM1 and TRPC1/Orai1 was also increased in prostate cancer cells when compared with control RWPE1 cells (Figure1G and H). Overall, these data indicate that Ca2+-mediated increase in cell proliferation and survival of prostate cancer cells, is perhaps due to increased STIM1 expression. In addition, increase in STIM1-TRPC1/Orai1 interaction could also facilitate Ca2+ entry via the SOCE mechanism that could promote cell survival and proliferation of prostate cancer cells.
Resveratrol (RSV) an antioxidant agent mainly concentrated in red grapes has been shown to decrease the risk of many cancers ; however the mechanism is not well defined. Thus we next evaluated if addition of resveratrol decreases cell proliferation and survival of prostate cancer cells. Cells treated with RSV for 24h showed a dose dependent decrease in the cell survival of prostate cancerous cells (PC3 and DU145) (Figure 2A and B). Similarly, cell proliferation was also decreased and both PC3 and DU145 cells, showed a significant decrease in BrdU incorporation (Figure 2C and D). Data presented in figure 1 suggest that increase in STIM1 expression and its interaction with TRPC1/Orai1 could be critical for increased cell proliferation/survival of prostate cancer cells. Therefore we also evaluated the expression of TRPC1, Orai1 and STIM1 in control and RSV treated prostate cancer cells. Importantly, no change in the overall or surface expression of TRPC1 or Orai1 was observed upon RSV treatment. In contrast a decrease in total STIM1 levels was observed in RSV treated cancer cells (P<0.05; Figure 2E-H). We and others have previously shown that upon store-depletion STIM1 is targeted to the ER-PM junctions where it interacts with TRPC1 channels [30,31]. Thus, co-immunoprecipitation experiments using STIM1 antibodies were performed in control and store-depleted conditions. Addition of thapsigargin (Tg, SERCA pump blocker), showed an increase in STIM1-TRPC1 interaction in both PC3 and DU145 cells, which was also decreased in RSV treatment cells (Figure 2I). These data suggest that RSV inhibit STIM1-TRPC1 functional interaction that could inhibit Ca2+ entry and induce cell death in prostate cancer cells.
Data presented thus far indicate that Ca2+ is essential for the proliferation/survival of prostate cancer cells and RSV treatment not only inhibit STIM1 expression, but also inhibit Tg-induced association between TRPC1 and STIM1. Furthermore, as TRPC1 is activated via STIM1, and this association is important for SOC-mediated Ca2+ entry, we next evaluated if SOCE is altered upon RSV treatment. To evaluate SOC-mediated Ca2+ entry, ER Ca2+ stores were depleted by the addition of thapsigargin (Tg, 2 μM). Importantly, in the absence of extracellular Ca2+ the increase in [Ca2+]i evoked by Tg (first peak) was significantly decreased in both PC3 and DU145 cells following RSV treatment, when compared with untreated cells (Figure 3A and B). Addition of external Ca2+ (1 mM), which initiates SOC-mediated Ca2+ entry, was also decreased in RSV treated PC3 and DU145 cells (Figure 3A and B), indicating that RSV treatment inhibits SOCE, which could be critical for decreasing cell proliferation/survival.
To establish the identity of the SOC channel, electrophysiological recordings were performed in prostate cancer cells. In PC3 cells, addition of Tg induced an inward current which was non-selective and reversed between 0 and −5mV (P<0.05; Figure 3C, D and F). The currents shown in figure 3C were recorded at a holding potential of −80 mV and I/Vs curves were developed using a ramp protocol where current density was evaluated at various membrane potential and plotted. Importantly, the channel properties were similar to those previously observed with TRPC1 channels , suggesting that TRPC1 could contribute to the endogenous SOC-mediated Ca2+ entry channel in PC3 cells. Similar results were also obtained with DU145 cells and the Tg induced inward currents were similar as observed with PC3 cells (data not shown) also the I/V curves were similar between the two cells (Figure 3E). Also, SKF 96365, a nonspecific TRPC channel blocker was used that showed a decrease in these inward currents in both PC3 and DU145 cells (data not shown). Importantly, addition of RSV significantly decreased SOC currents in both PC3 and DU145 cells without altering the current-voltage (I-V) relationship (Figure 3C-F). Collectively, these results suggest that RSV decreases ER Ca2+ by diminishing SOC-mediated Ca2+ entry, which could lead to the activation of the UPR in these cells that together would induce cell death.
To understand the mechanism(s) of RSV mediated decrease in cell survival, we investigated the unfolded protein response (UPR) as loss of ER-Ca2+ has been shown to induce ER stress . UPR markers (GRP78 and CHOP) were upregulated at the protein levels in RSV-treated cells, whereas no change in GRP94 was observed (Figure 4A). Quantification of GRP78 was shown in Figure 4C (P<0.05). Furthermore, RSV was previously shown to induce autophagy, thus we next evaluated the induction of autophagy in control and RSV treated cancer cells. Importantly, in both PC3 and DU145 cells, RSV treatment showed an increase in LC3B-II, but did not showed an increase in Beclin1 (P<0.05; Figure 4B and C), suggesting that perhaps the autophagy induced by RSV is independent of Beclin1. In addition, 100μM RSV treatment resulted in accumulation of GFP-LC3 puncta in PC3 and DU145 cells, however lower dose of RSV, 10μM failed to show a significant accumulation of GFP-LC3 when compared with control untreated cells (Figure 4D and E). Since the RSV-induced autophagy was independent of Beclin1, we next investigated if it was mediated via the mTOR pathway. Furthermore, Ca2+ entry has been shown to activate the AKT/mTOR pathway, which is essential for inhibition of cell death. Importantly, RSV treatment attenuated the activation of mTOR, a kinase that regulates cell survival, in both PC3 and DU145 cells (Figure 4F). Activation of p70S6K and S6ribo that are downstream of mTOR were also inhibited in the presence of RSV (Figure 4F). Finally, RSV treatment also significantly decreased AKT1 phosphorylation (AKT473) without affecting total AKT1 levels in prostate cancer cells (Figure 4F). Quantification of phospho-mTOR, phospho- AMPKα and phospho-AKT473 were shown in Figure 4G (P<0.05). These results strongly suggest that RSV-mediated loss of Ca2+ influx could be essential for the activation of the protective AKT1/mTOR activation in prostate cancer cells.
To better understand the link between Ca2+ influx and cell survival, we inhibited SOCE. Addition of SKF96365 that has been shown to block SOC-mediated Ca2+ entry , significantly decreased Tg-induced Ca2+ entry in PC3 cells (Figure 5A and B). Similar results were also obtained with DU145 cells where SKF96365 treatment inhibited SOC-mediated Ca2+ entry (data not shown). Importantly, increasing SKF96365 concentration significantly decreased cell survival in both DU145 and PC3 cells (Figure 5C and D). Similarly, cell proliferation was also decreased under these conditions and again both DU145 and PC3 cells showed a significant decrease in BrdU incorporation in the presence of increasing SKF96365 (Figure 5E and F). Consistent with these data, SKF96365 treatment also showed an increase in LC3A/B in PC3 and DU145 cells (P<0.05; Figure 5G and H); however the effect in PC3 cells was more prominent. Our data presented in figure 4 also showed that the AKT/ mTOR pathway was important and, SKF96365 treatment inhibits the activation of mTOR and AKT1 in both PC3 and DU145 cells (Figure 5I). Together, these data suggest that inhibition of Ca2+ entry leads to decreased cell proliferation/survival of prostate cancer cells via the inhibition of the AKT/ mTOR pathway.
To further establish that indeed RSV-mediated loss in Ca2+ influx (due to loss of STIM1 expression) is essential for cell death, we overexpressed STIM1 in PC3 cells. Expression of STIM1 plasmid, showed increased STIM1 expression, whereas no increase in control actin levels was observed (Figure 6A). Importantly, RSV-dependent inhibition of SOC-mediated Ca2+ entry was also restored in cells that overexpress STIM1 (Figure 6B and C). Finally, both cell survival and cell proliferation was restored in cells that overexpress STIM1 and were treated with various doses of RSV (Figure 6D and E). Furthermore, phosphorylation of mTOR was also restored in STIM1 overexpressing cells that were treated with RSV (Figure 6F and G). Consistent with these results, both LC3A and CHOP expression that induces cell death, were decreased in STIM1 overexpressing cells that were treated with RSV (Figure 6F and G). Overall, these results suggest that increase in STIM1 expression, restores RSV-dependent loss in Ca2+ entry and inhibits RSV-mediated inhibition of cell proliferation and survival. These results also suggest a mechanism as why some cancer cells are resistant to cell death upon RSV treatment- as a threshold of STIM1 expression is perhaps critical for RSV-mediated cells death.
Cytosolic Ca2+ mediates several cellular signaling pathways that are related to proliferation, differentiation, and migration of tumor cells . The Ca2+ influx from the extracellular space and Ca2+ release from the intracellular sources determine the cytosolic Ca2+ concentration. Previously, we have shown that increase in serum Ca2+/Mg2+ ratio promote prostate cancer epithelial cell proliferation by activating TRPM7, which function as an endogenous MagNuM channel in prostate cancer cells. Furthermore, decrease in the Ca2+ to Mg2+ ratio, facilitated Ca2+ entry and led to an increase in cell proliferation of cancer cells . Therefore, changes in the expression or function of Ca2+ channels could affect the cytosolic Ca2+ homeostasis and its dependent cellular process, such as proliferation and survival. Moreover, the role of Ca2+ in autophagic cell death has also been recently elucidated in cancer cells and studies have also shown that the cytosolic Ca2+as a major regulator of both basal and induced autophagy .
Interestingly, the anti-carcinogenic activity of dietary polyphenol, RSV has been widely studied both in vitro and in vivo tumor models, including prostate cancer [21,22,25]. It is well known that RSV induces cell cycle arrest, inhibits cell proliferation and activates apoptosis in androgen-independent prostate cancer cells [24,37]. The present study, in conjunction with previous studies, demonstrates that RSV inhibits prostate cancer cell proliferation and induces autophagy in PC3 and DU145 cells. Several mechanisms have been shown to mediate the antiproliferative effects of RSV in prostate cancer cells, however the precise mechanism of RSV-mediated growth inhibition and the involvement of Ca2+ remain unclear. Several phase I and phase II clinical trials are currently in progress at the National Institute of Health (http:/clinicaltrials.gov) for therapeutic effect of RSV against several cancer types including patients with colon cancer and lymphoma , however there are no results from prostate cancer patients. Understanding the downstream signaling mechanisms of resveratrol-induced cell death may facilitate the development of additional therapeutic targets for the androgen-independent prostate cancer prevention and treatment. The results of this study demonstrate that STIM1 is an important target of RSV for inhibiting cell proliferation and to activate ER stress mediated autophagic cell death in androgen-independent prostate cancer epithelial cells.
Store operated Ca2+ entry is the predominant Ca2+ influx mechanism in prostate cancer cells. Substantial progress has been made throughout the last two decades in the elucidation of the key players of SOCE and mechanisms responsible for SOCE activation in both excitable and non-excitable cells. Importantly, these studies have identified an involvement of TRPCs and/or Orai1 channels in SOCE. Indeed, Stim1 have also been identified recently as the molecular switch that modulate SOC channels and its significance in SOCE have been elucidated in androgen-dependent prostate cancer cells [15,39]. Nevertheless, it is unclear about the targets and mechanisms by which SOCE exerts its effects on cell function and survival in androgen-independent prostate cancer cells. The data presented here show that SOCE is increased in androgen-independent cells, DU145 and PC3 when compared with normal prostate epithelial cells, RWPE1. MTT assay and BrdU incorporation demonstrated that external Ca2+ mediates the survival and proliferation of DU145 and PC3 cells. These results are consistent with other reports showing that the anti-proliferative effect of external Ca2+ and SOCE in cancer cell [6,20,40]. Moreover, ER Ca2+ depletion and subsequent Ca2+ influx through SOCE have been previously shown to be critical in promoting growth arrest and apoptosis of prostate cancer epithelial cells [4,13].
To address the role of SOCs, we studied the expression of TRPC1, Orai1 and STIM1 level in normal and prostate cancer cell. Our results clearly showed that there were no significant difference in the protein levels of TRPC1 and Orai1; whereas STIM1 levels were increased in cancer cells when compared with control cells. Moreover, the interaction of STIM1 with TRPC1 and Orai1 was also increased in cancer cells. STIM1 is an ER resident protein, monitor the Ca2+ level in the ER by luminal EF Ca2+ binding domain and translocate upon store depletion to plasma membrane to activate SOCE channels . These results suggest that STIM1 interaction with either Orai1 or TRPC1 causes an increase in SOCE in androgen-independent prostate cancer cells. Studies have also shown that molecular components of SOCs, particularly Orai1, TRPC1 and STIM1 seem to play a crucial role in cell proliferation and migration in several human cancers notably, breast, renal, cervical, and lung cancers indicating that inhibition of SOCE suppresses tumorigenicity [41,42]. The data presented here supports the hypothesis that Ca2+ entry through SOCE channels may activate the Ca2+ dependent signaling process such as proliferation and survival that are critical for carcinogenesis, in androgen-independent prostate cancer cells.
Our current study demonstrates that RSV prevents cell proliferation and induces cell death in a dose-dependent manner. Interestingly, 100μM RSV for 24h, abolishes both ER Ca2+ release as well as SOCE in DU-145 and PC-3 cells by decreasing STIM1expression. However, the expression pattern of TRPC1 and Orai1 was not affected upon RSV treatment, but, RSV treatment decreases the STIM1-TRPC1 interaction upon store depletion. Previous study has shown that alteration in the expression of SOC’s, particularly Orai1, contribute to the increased resistance of prostate cancer cell towards induction of apoptosis. Our data substantiate the recent study indicating that STIM1 may play an important role in the development of prostate cancer and inhibition of its expression induces cell death in PC3 cells . A growing number of studies have also shown that blockade or knockdown of STIM1 or TRPC1 significantly inhibits the proliferation and migration of cancer cell [41,43]. However, the underlying mechanisms seem to involve the reduction of SOCE upon STIM1 knockdown which suppress the carcinogenic cytosolic Ca2+ signaling in cancer cells. Our data is quite promising in which we found that RSV induces cell death by decreasing STIM1 expression and subsequent SOCE in androgen independent DU145 and PC3 cells. Several pieces of our data also support the conclusion that RSV inhibits prostate cancer cell proliferation by reducing SOCE. For example, RSV decreases the expression of STIM1 and dissociates the association of TRPC1-STIM1 and Orai1-STIM1 in DU145 and PC3 cells. Inhibition of SOCE by SKF-96365 decreases the survival and proliferation of DU145 and PC3 cells whereas, restoration of SOCE via STIM1 overexpression attenuated the RSV induced cell death. Overall, these results suggested that STIM1 is a primary target of RSV for mediating its anti-carcinogenic activity. However, it should be noted that RSV also regulates several other mechanisms including ER stress and autophagy via STIM1 and SOCE dependent manner.
Resveratrol was shown to induce pro-apoptotic endoplasmic reticulum stress in several cancer cells [44,45]. However, the exact mechanisms that proceed the cancer cells to ER stress under RSV treatment is not yet unveiled. Depletion of ER Ca2+ is known to cause ER stress and the current study have shown that RSV decreases SOCE, a vital mechanisms for ER Ca2+ store refilling, which ultimately could result in the depletion of ER Ca2+ store in DU145 and PC3 cells. As expected, Ca2+ release from the internal stores was significantly decreased upon RSV treatment. The shortage of ER Ca2+ may causes a deterioration in the protein folding in the lumen of the ER and causes ER stress [33,46]. Consistent with this, we found that RSV significantly induced ER stress, such as upregulation of GRP78/Bip, and CHOP/GADD153 protein. Induction of GRP78, also called Bip, may be a pro-survival mechanism of the cells, since it assists in the folding of nascent unfolded proteins, prevents the Ca2+ efflux from the ER to the cytosol, and alleviating ER stress induced apoptotic stimuli . However, if the ER stress persists, cells induce the expression of CHOP, a unique transcription factor that mediates the ER stress induced apoptosis. Induction or overexpression of CHOP sensitizes cells to ER stress mediated apoptosis whereas knockdown or deletion of protects the cell from apoptosis . However, our results have shown that RSV treatment in DU145 and PC3 cells resulted in increased autophagy. Based on our results we may hypothesis that treatment of prostate cancer cells with RSV will lead to ER Ca2+ depletion and subsequent ER stress, which itself might also be a trigger for autophagy.
Autophagy is a catabolic process for the degradation and recycling of macromolecules and organelles, which is activated during stress conditions. Autophagy has a dual role in cancer cells likely this could be a survival or cell death mechanisms. For example, autophagy mediated cell death is the predominant cell death mechanisms in response to certain anti-cancer drugs [49,50]. On the contrary, autophagy activates pro-survival mechanisms that attenuates anti-cancer drug induced apoptosis . Several natural compounds, such as curcumin, paclitaxel, oridonin, quercetin and fisetin, have been shown to induce autophagy mediated cell death in a variety of tumor cells [52,53]. Thus, dietary natural compounds that induce autophagy may be of potential use as anticancer agents. Several studies have also shown that RSV is capable of inducing autophagy in different cancer cell line models [52,53]. Scarlatti and colleagues reported that RSV activates noncanonical Beclin-1–independent autophagy in MCF-7 cells . Similarly, RSV promotes autophagic cell death in chronic myelogenous leukemia cells through both JNK-mediated p62 expression and AMPK activation, and stimulates both apoptosis and autophagy in ovarian carcinoma cells [55,56]. Opipari et al., reported that resveratrol inhibited cell proliferation and induced autophagocytosis in ovarian carcinoma cell lines . Several studies have further shown that resveratrol induces apoptosis mediated cell death in a variety of cancer cells including prostate cancer cell lines [25,52,53]. In this study, we observed that in androgen-independent prostate cancer cells, RSV activates ER stress-mediated autophagy that was independent of Beclin1. LC3 is widely considered the marker for autophagy since during autophagosome formation, LC3 (cytosolic microtubule associated protein light chain 3) is processed and conjugated with phosphatidylethanolamine (PE) and inserted into autophagic vesicle membranes [58,59]. The expression and accumulation of LC3 was robustly increased in RSV treated cells, albeit only at higher doses, which confirms that RSV induced autophagic flux.
Several signaling pathways are known to regulate autophagy including the ERK, PI3K class I and II, and mTOR. The mTOR signaling pathways regulate various cellular process including autophagy through coordinating several signaling molecules such as S6K, 4EBP-1 and AKT. The mTOR/AKT pathway is an important signaling mechanism that regulates different cellular process including cell survival, proliferation, apoptosis and autophagy [60,61]. Indeed it has been shown that the mTOR/AKT pathway is critical for prostate tumor growth and survival, especially when the PTEN, a tumor suppressor gene, is mutated . Moreover, overexpression and uncontrolled activation of AKT have been identified in several human cancers including prostate cancer [63,64]. Similarly, inactivation of mTOR pathway shown to inhibit prostate cancer cell growth, migration and invasion . Interestingly, the role of mTOR in SOCE activation has been elucidated recently in tuberous sclerosis complex-related tumor development. The present study has shown that mTORC1 activates SOCE, and augmented SOCE by hyperactive mTORC1-STIM1 cascade may contribute to the benign nature of tuberous sclerosis complex (TSC)-related tumors. Interestingly, mTORC1 inhibitor, rapamycin suppressed the SOCE by decreasing the expression of STIM1 in tuberous sclerosis complex 2(TSC2) deficient MEF cells . Hence, it is suggested that to develop a drug that can inhibit both mTOR and other signaling molecules PI3K/AKT would be an effective strategy in treating prostate cancer. Consistent with these studies, we observed that RSV treatment activates the AMPK and inhibits the mTOR/AKT phosphorylation. The results suggest that RSV induces autophagy through regulating mTOR/AKT pathways. However, the RSV induced autophagy was abolished in STIM1 overexpressed PC3 cells. The STIM1 overexpression reverts the RSV induced SOCE suppression, ER stress and cell death which indicates that RSV targets SOCE via suppressing STIM1 and deplete ER store causes ER stress induced autophagic cell death in androgen-independent prostate cancer cells. Moreover, the signaling pathways by which RSV regulates autophagy induction and exerts its anti-carcinogenic effects are far from being completely elucidated. Although several studies suggest that increase in intracellular Ca2+ may contribute to anti-carcinogenic effect, this has never been clearly proven. Nevertheless, further investigations are needed to elucidate the molecular mechanisms by which STIM1 regulate prostate cancer cell proliferation and survival.
In conclusion, SOCE is crucially involved in the survival and proliferation of androgen-independent prostate cancer cell lines, DU145 and PC3, and resveratrol treatment attenuates SOCE and induce autophagy mediated cell death. The mechanisms involves altered expression of STIM1 and subsequent SOCE influx which cause an ER stress response in DU145 and PC3 cells. ER stress further potentiate the autophagy mediated cell death through regulating mTOR/AKT pathways. To the best of our knowledge, this is the first report that RSV induces autophagic cell death by regulating the function of STIM1 and subsequent SOCE.
We thank the confocal facility at UND which is partially supported by the NIH COBRE grant (P30GM103329). We duly acknowledge grant support from the NIH (DE017102) awarded to B.B.S.