Cisplatin-induced caspase activation mediates PTEN cleavage in ovarian cancer cells: a potential mechanism of chemoresistance
© Singh et al.; licensee BioMed Central Ltd. 2013
Received: 27 November 2012
Accepted: 27 April 2013
Published: 10 May 2013
The phosphatase and tensin homolog deleted on chromosome 10 (PTEN) tumor suppressor protein is a central negative regulator of the PI3K/AKT signaling cascade and suppresses cell survival as well as cell proliferation. PTEN is found to be either inactivated or mutated in various human malignancies. In the present study, we have investigated the regulation of PTEN during cisplatin induced apoptosis in A2780, A270-CP (cisplatin resistant), OVCAR-3 and SKOV3 ovarian cancer cell lines.
Cells were treated with 10μM of cisplatin for 24h. Transcript and protein levels were analysed by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) and western blotting, respectively. Immunofluorescence microscopy was used to assess the intracellular localization of PTEN. Proteasome inhibitor and various caspases inhibitors were used to find the mechanism of PTEN degradation.
PTEN protein levels were found to be decreased significantly in A2780 cells; however, there was no change in PTEN protein levels in A2780-CP, OVCAR-3 and SKOV3 cells with cisplatin treatment. The decrease in PTEN protein was accompanied with an increase in the levels of AKT phosphorylation (pAKT) in A2780 cells and a decrease of BCL-2. Cisplatin treatment induced the activation/cleavage of caspase-3, -6, -7, -8, -9 in all cell lines tested in this study except the resistant variant A2780-CP cells. In A2780 cells, restoration of PTEN levels was achieved upon pre-treatment with Z-DEVD-FMK (broad range caspases inhibitor) and not with MG132 (proteasome inhibitor) and by overexpression of BCL-2, suggesting that caspases and BCL-2 are involved in the decrease of PTEN protein levels in A2780 cells.
The decrease in pro-apoptotic PTEN protein levels and increase in survival factor pAKT in A2780 ovarian cancer cells suggest that cisplatin treatment could further exacerbate drug resistance in A2780 ovarian cancer cells.
KeywordsCisplatin Caspases Cancer Apoptosis PTEN
The tumor suppressor phosphatase and tensin homolog (PTEN) is negative regulator of the PI3K/AKT pathway . Decrease in PTEN levels could lead to increase in phosphorylation and activation of AKT, which further promotes cell survival and proliferation . Phosphatase activity of PTEN is known to be responsible for the regulation of apoptosis, proliferation and cell migration [3, 4]. Epigenetic and genetic changes in PTEN are the crucial factors for PTEN activity and PTEN is mostly found to be deleted or mutated in various human cancers . Ovarian cancer is one of the leading gynecologic malignancy. After surgical intervention for ovarian cancer, cisplatin based chemotherapy is the mainstay for treatment. Major challenge to fight ovarian cancer is the development of chemoresistance. In spite of the extensive research in the field of cancer, certain mechanism of chemoresistance remained unresolved.
Chemotherapeutic drugs like cisplatin are known to act by inducing apoptosis. During apoptosis, a structurally related group of cysteine proteases known as caspases mediate protein cleavage [6, 7]. Caspases can be classified into two groups, more precisely initiator and effector caspases. Initiator caspases group includes caspase-6, -8, -9, and −10; they are responsible in initiating a proteolytic cascade by activating the pro-caspases to amplify the death signal. The second group, consists of caspase-2, -3, and −7, are known as effector caspases; they are activated by the initiator caspases . A plethora of caspase substrates have been identified till date and the list is expanding fast .
Previous studies suggest that PTEN can be regulated at the transcriptional and post-translational levels through multiple molecular pathways [10–12]. Recently, it has been found that microRNAs can also target PTEN, regulate AKT signaling pathway and induce cisplatin chemoresistance in ovarian cancer cells . Treatment with cisplatin activates the caspases cascades in the cells, which further leads to the induction of apoptosis [14–16]. Recent study from our lab determined that cisplatin induced activation of caspase-3 can cleave tumor suppressor Par-4 protein, associated with selective killing of cancer cells, suggesting that activated caspases could target cellular proteins involved in tumor suppression . It has been shown that caspase-3 can cleave PTEN in HEK293 cellular extracts and furthermore demonstrated that C-terminal cleavage by caspase-3 is negatively regulated by phosphorylation of Ser370 and/or Ser385. Based on these studies, we hypothesize that cisplatin induced caspase activation could target PTEN in ovarian cancer cells. The outcomes of the present study indicate that cisplatin mediated caspases activation leads to the cleavage of PTEN which results in AKT phosphorylation in ovarian cancer cells suggesting that cisplatin based chemotherapy could induce chemoresistance by targeting PTEN in ovarian cancer cells.
Cisplatin treatment decreases PTEN protein levels
Cisplatin treatment promotes phosphorylation of AKT
Proteasomal degradation of PTEN in presence of cisplatin
Caspases activation and levels of anti-apoptotic molecules
Role of caspases in PTEN protein degradation
PTEN is a putative tumor suppressor protein and a key regulatory molecule of AKT signaling pathway. PTEN possesses lipid phosphatase activity against 3-phosphoinostides opposing PI3K, finally negatively regulating AKT phosphorylation . In the present study, we demonstrate the role of caspases in the regulation of PTEN levels during cisplatin induced apoptosis. In this study we have found that cisplatin induced activation of multiple caspases leads to proteolytic cleavage of PTEN in A2780 cells. Cisplatin treatment induced PTEN degradation in A2780 cells is indicative of post-translational regulation. The activation of AKT by PIP3 production initiates multiple signaling pathways by phosphorylating various downstream targets and by inactivating the inhibitors of cell cycle, protein synthesis glycolysis and angiogenesis. Summarily, it can be said that AKT paves the way for oncogenesis [20, 21]. The decrease in PTEN levels leads to the activated form of AKT which could further promotes cellular proliferation and survival in A2780 cells. We have not observed any change in AKT phosphorylation in A2780-CP, OVCAR-3 and SKOV3 cells which could be due the fact that there was no change in the PTEN levels, suggesting that there is a direct relationship between these two proteins in ovarian cancer cells. In addition, cisplatin prevents the nuclear localization of PTEN in A2780 cells which is in accordance with our previous study. In the latter study XIAP knockdown prevents nuclear localization of PTEN, we have also observed that XIAP levels are decreased upon cisplatin treatment which could prevent the nuclear localization of PTEN in the present study. Proteins can undergo proteasomal degradation under external stimuli [22, 23]. To validate this hypothesis, we pretreated the cells with MG132, a proteasomal inhibitor and subsequently treated with cisplatin. However there was no restoration of PTEN levels in presence of MG132 and cisplatin (Figure 4; Lane 4). Low levels of PTEN was also observed in the only MG132 treated cells because MG132 itself is an apoptotic agent, which further activates caspase-3 (Figure 4; Lane 3) and this activation of caspase −3 could lead to a decrease in the level of PTEN as compared to control (Lane 1). This result is in accordance with previously published report . Collectively the results from the present study suggest that PTEN does not undergo proteasomal degradation in the presence of cisplatin in A2780 cells.
Cisplatin treatment can initiate both the intrinsic and extrinsic pathways of caspases activation . The activation of various initiator and effector caspases in A2780, OVCAR-3 and SKOV3 cells except A2780-CP cells is indicative of the activation of both apoptotic pathways. However, no particular caspases activation difference was observed among individual cell lines. We could not find out the involvement of any particular caspase in the PTEN degradation from these results. Cell fate is determined by a delicate balance between pro-apoptotic and anti-apoptotic factors . XIAP can inhibit caspase-3 and caspase-7 by directly binding to them . Previous studies have shown that IAPs can inhibit caspases directly or indirectly [17, 18] and we have shown that XIAP overexpression can induce chemoresistance in A2780 cells, while XIAP antisense downregulation leaded to increased sensitivity in A2780-CP cells . All the IAPs (BCL-2, cIAP-1, survivin and XIAP) studied in A2780 cells were found be decreased upon cisplatin treatment. However, decreased survivin levels were observed in SKOV3 cells and decreased in cIAP-1 protein levels were seen in OVCAR-3 cells in the presence of cisplatin. As PTEN levels remained stable in SKOV3 and OVCAR-3 cells, we could rule out the role of survivin and c-IAP-1 in caspase mediated PTEN degradation. However, we have observed low endogenous level of BCL-2 in A2780 cells and furthermore BCL-2 level was almost diminished after cisplatin treatment. Decreased levels of BCL-2 could be the reason for higher activation of caspases in A2780 cells owing greater sensitivity than other cell line tested and cleavage of PTEN by activated caspases. Finally, pretreatment with specific caspases inhibitors restored PTEN levels in cisplatin treated cells suggesting the involvement of more than one caspase in PTEN degradation. This result further suggests that PTEN protein sequence contains multiple cleavage sites.
This study provides the first evidence that PTEN protein can be targeted during cisplatin induced caspases activation in A2780 cells. Caspases-mediated decrease in PTEN levels further affect AKT signaling pathway, which plays an important role in regulating chemosensitivity in ovarian cancer. The present study could provide new insights to understand cisplatin-induced chemoresistance in ovarian cancers and could explain underlying mechanisms involved in PTEN regulation.
Human ovarian cancer cell lines A2780, A2780-CP (cisplatin resistant), cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM/F12) supplemented with 2% BGS (Bovine Growth Serum) (Thrmo Scientific, Rockford, IL) and 50μg/ml of gentamicin. OVCAR-3 cells were cultured in RPMI-1640 supplemented with 10% FBS (Fetal Bovine Serum) (Thrmo Scientific, Rockford, IL) and 50μg/ml of gentamicin. SKOV3 cells were cultured in Mc-Coy’s medium supplemented with 10% FBS and 50μg/ml of gentamicin.
Reagents and antibodies
AKT total (9272), phospho-AKT (9271), BCL-2 (2872), C-IAP1 (7065), cleaved-caspase-3 (9661), cleaved-caspase-6 (9761), cleaved-caspase-7 (9491), cleaved-caspase-8 (9748), cleaved-caspase-9 (9505), PTEN (9559), phospho-PTEN (9554), Survivin (3879) and XIAP (2042) antibodies were purchased from Cell Signaling (Danvers, MA). Anti-GAPDH(HRP) antibody (9385) was procured from Abcam Inc. (Cambridge, MA) Cisplatin, Proteasomal inhibitor (MG132), and Hoechst 33248 were obtained from Sigma-Aldrich (St. Louis, MO). Broad range Caspase-3 Inhibitor II [Z-DEVD-FMK (264156)], Caspase-3 Inhibitor VII (219012), Caspase-6 Inhibitor I [Z-VEID-FMK (218757)] and Caspase-8 Inhibitor I [IETD (218773)] were obtained from Calbiochem (San Diego, CA).
Western blot analysis
Following different treatments cells were washed with PBS and submitted to lysis in cold radioimmune precipitation assay (RIPA) lysis buffer containing protease inhibitors (Complete™ from Roche Applied Science) followed by three freeze-thaw cycles. Equal amounts of cell lysates (as determined using Bio-Rad DC protein assay) were separated onto 10%-15% polyacrylamide gels and then transferred onto nitrocellulose membranes (Bio-Rad, Hercules, CA). The membranes were blocked with 5% milk in PBS containing 0.05% Tween 20 for 1h at room temperature, overnight incubated with primary antibody, washed in PBS with 0.05% Tween 20, and probed with horseradish peroxidase-conjugated secondary antibody (Bio-Rad, Hercules, CA). Protein detection was performed using SuperSignal West Femto™ substrate (Thremo Scientific, Rockford, IL), as described by the manufacturer.
RNA isolation and quantitative-RT-PCR (Reverse Transcription-Polymerase Chain Reaction)
Total RNA was isolated from cells using Purelink™ RNA Mini Kit (Cat no. 12183020 Invitrogen, Carlsbad, CA) according to the manufacturer's instructions. First strand cDNA was synthesized from 1μg of RNA using qScript™ cDNA Supemix (Quanta Biosciences Inc. Gaithersburg, MD). Primers used for amplification were as follows: (i) PTEN forward 5’-ACCCCTTCATTGACCTCAACTA-3’ and reverse 5’-TCTCGCTCCTGGAAGATGGTGA-3’ (ii) GAPDH forward 5’-TGAAGGCGTATACAGGAACAAT-3’ and reverse 5’-CGGTGTCATAATGTCTTTCAGC-3’. PCRs were conducted in LightCycler (Roche). Data were analyzed by using LightCycler Software Version 4.1.
Transient transfection using BCL-2 plasmid
BCL-2 (pcDNA3 BCL-2) and empty (pcDNA3) plasmids were purchased from Addgene. One day before transfection, cells were plated at 3×105/well to achieve a confluency of ~70% .Next day cells were transfected with 2μg of expression vector using Fugene6 (Roche, Indianapolis, IN) according to manufacturer’s instructions. Cells were incubated for 48h at 37°C, and the medium was replenished with fresh medium containing cisplatin (10μM). The plates were incubated for an additional 24h before the cells were collected.
Confocal immunofluorescent analysis
Cells were grown on to sterile coverslips in 6 well plates. After cisplatin treatment, cells were fixed with 4% paraformaldehyde for 10min, and washed twice with PBS for 5min. Cells were permeabilized using permeabilizing solution (0.1% Triton, 0.1% sodium citrate) for 10min followed by incubation with Dako blocking serum for 1h. After blocking, cells were incubated with the PTEN primary antibodies or isotypic control antibodies. Both were diluted at a ratio of 1/100 for 1h. After washing with PBS, cells were incubated with fluorescent tag conjugated secondary antibodies (as mentioned in figure legends) for 30min in dark. Cells were counter stained with Hoechst 33248 (0.25μg/ml) for 5min, slides were mounted using slowfade gold anti-fading reagent (Invitrogen) and viewed under Carl Zeiss Axio observerZ1 microscope.
All the experiments were repeated three times. Data were subjected to one-way ANOVA (PRISM software version 4.0; GraphPad, San Diego, CA) followed by Newman-Keuls test to determine the differences between the experimental groups. Differences were considered significant at the level of P < 0.05.
We are grateful to Sophie Parent and Valerie Leblanc for their technical assistance throughout the study. This work has been supported by a grant from the Canadian Institutes for Health Research (MOP-66987). E.A. holds a Canadian Research Chair in Molecular-Gyneco-Oncology.
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