Comparative evaluation of the treatment efficacy of suberoylanilide hydroxamic acid (SAHA) and paclitaxel in ovarian cancer cell lines and primary ovarian cancer cells from patients
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In most patients with ovarian cancer, diagnosis occurs after the tumour has disseminated beyond the ovaries. In these cases, post-surgical taxane/platinum combination chemotherapy is the "gold standard". However, most of the patients experience disease relapse and eventually die due to the emergence of chemotherapy resistance. Histone deacetylase inhibitors are novel anticancer agents that hold promise to improve patient outcome.
We compared a prototypic histone deacetylase inhibitor, suberoylanilide hydroxamic acid (SAHA), and paclitaxel for their treatment efficacy in ovarian cancer cell lines and in primary patient-derived ovarian cancer cells. The primary cancer cells were isolated from malignant ascites collected from five patients with stage III ovarian carcinomas. Cytotoxic activities were evaluated by Alamar Blue assay and by caspase-3 activation. The ability of SAHA to kill drug-resistant 2780AD cells was also assessed.
By employing the cell lines OVCAR-3, SK-OV-3, and A2780, we established SAHA at concentrations of 1 to 20 μM to be as efficient in inducing cell death as paclitaxel at concentrations of 3 to 300 nM. Consequently, we treated the patient-derived cancer cells with these doses of the drugs. All five isolates were sensitive to SAHA, with cell killing ranging from 21% to 63% after a 72-h exposure to 20 μM SAHA, while four of them were resistant to paclitaxel (i.e., <10% cell death at 300 nM paclitaxel for 72 hours). Likewise, treatment with SAHA led to an increase in caspase-3 activity in all five isolates, whereas treatment with paclitaxel had no effect on caspase-3 activity in three of them. 2780AD cells were responsive to SAHA but resistant to paclitaxel.
These ex vivo findings raise the possibility that SAHA may prove effective in the treatment of paclitaxel-resistant ovarian cancer in vivo.
KeywordsOvarian Cancer Paclitaxel Ovarian Cancer Cell SAHA Ovarian Cancer Cell Line
histone deacetylase inhibitors
suberoylanilide hydroxamic acid
Ovarian cancer is the most lethal gynaecological neoplasm, accounting for over 6% of deaths from cancer in women . The standard treatment is a combination of surgery and chemotherapy, the latter usually consisting of a taxane/platinum combination. By this regimen, initial response rates of more than 80% are achieved . Unfortunately, in the vast majority of women, diagnosis occurs after the disease has already disseminated beyond the ovaries. These patients typically relapse and eventually die as the tumours become refractory to treatment. Actually, drug resistance is supposed to account for therapy failure and death in more than 90% of ovarian cancer patients with advanced-stage at diagnosis . Novel treatment strategies to overcome drug resistance, thus, are urgently needed.
Drug resistance is generally associated with altered gene expression in the drug-resistant cancer cells in comparison to the drug-sensitive cancer cells. Typically, resistant tumour cells show an upregulation of antiapoptotic proteins and a downregulation of proapoptotic proteins, resulting in a ratio of anti- to proapoptotic proteins favouring survival, as well as an elevated expression of drug efflux pumps, such as P-glycoprotein (Pgp) . In ovarian cancer, cDNA microarray analyses of cisplatin-resistant sublines of KF-1 cells  and paclitaxel-resistant sublines of SK-OV-3 cells  have demonstrated transcriptional changes in genes coding for such proteins. Hence, treatment strategies aiming at reversing the aberrant expression of genes involved in drug response could prove effective in the management of drug-resistant ovarian cancer.
At present, considerable attention focuses on the role of epigenetic modifications in carcinogenesis and the development of drug resistance. As such, histone hypoacetylation has recently been recognized as an important type of epigenetic alteration in human cancers . Histone hypoacetylation, which is associated with condensed chromatin structure and gene silencing, is the result of the aberrant actions of histone acetyltransferases and histone deacetylases. Inhibitors of histone deacetylases (HDIs) are currently emerging as a promising new class of anticancer agents: they can reactivate gene expression and prevent proliferation, activate differentiation, and/or induce apoptosis of tumour cells . In so doing, they e.g. reactivate gene expression of dormant tumour suppressor genes, such as CDKN1A (p21) .
The potent antitumour activity of HDIs has been observed in cell lines originating from different types of human cancers as well as in studies on mice xenograft models of human neoplasia . Importantly, HDIs have been shown both in vitro and in vivo to affect cancer cells while leaving normal cells comparatively unscathed [11, 12]. In addition, the clinical potential of these agents has been documented by several Phase I trials of different HDIs in patients with solid tumours or leukaemias [13, 14, 15, 16, 17, 18]. With respect to ovarian cancer, several preclinical studies have demonstrated the anticancer efficacy of various HDIs in cell lines in vitro [19, 20, 21, 22, 23] and in cell lines implanted into nude mice [24, 25]. However, no information is available about the potential effectiveness of HDIs in primary ovarian cancer cells from patients. Herein, we demonstrate efficient ex vivo activity of the HDI suberoylanilide hydroxamic acid (SAHA) in patient-derived ovarian cancer cells, which display only marginal responsiveness to paclitaxel.
OVCAR-3, SK-OV-3, A2780 and 2780AD ovarian carcinoma cells were kindly provided by Dr. J. Braunger (Altana Pharma, Konstanz, Germany). SK-OV-3 cells were maintained in McCoy's 5a. OVCAR-3, A2780, and 2780AD cells were maintained in RPMI 1640. The medium of OVCAR-3 cells was supplemented with 1.5 g/l sodium bicarbonate, 1.0 mM sodium pyruvate, and 0.01 mg/ml bovine insulin; the medium of 2780AD cells was supplemented with 2.2 μM doxorubicin (Sigma, Deisenhofen, Germany). All media were supplemented with 10% fetal calf serum, 2 mM L-glutamine, 100 units/ml penicillin G sodium, and 100 μg/ml streptomycin sulphate (media and supplements were purchased from Biochrom, Berlin, Germany). Cells were cultivated at 37°C in a humidified 5% CO2 incubator and routinely passaged when 90–95% confluent. Cell viability was determined by the trypan blue exclusion test. Cells were regularly inspected to be free of Mycoplasma with Mycoplasma detection reagents from Roche (Mannheim, Germany).
Isolation of primary ovarian cancer cells from ascites
The use of patient samples was approved prior to the initiation of these studies (University of Greifswald, Research Ethics Committee), and all patients signed consent forms. Ovarian cancer cells were isolated from malignant ascites collected from patients with stage III ovarian carcinomas. Of the five patients whose cells were used in this study, four were untreated, and one had been treated with a single dose of paclitaxel/carboplatin (isolate ASC-OC-4). The four untreated patients were subsequently treated with a palitaxel/carboplatin combination according to the standard protocol for the management of ovarian cancer.
The ascitic fluid was centrifuged at 3000 rpm at room temperature for 10 minutes, and the cellular pellet was washed twice in PBS. The pellet was resuspended in Ham's F12K medium (Biochrom) supplemented with 10% fetal calf serum, 2 mM L-glutamine, 100 units/ml penicillin G sodium, and 100 μg/ml streptomycin sulphate, and plated in T75 flasks. Ascitic fluid typically contains a considerable number of blood cells; however, they do not impede cell plating. After 3–4 weeks of culture, purity of the ovarian carcinoma cells was at least 80%. All experiments described here were performed at culture passages 4–7.
The assays were performed in quadruplicate in 96-well flat-bottom microtiter plates. After a 72-h incubation with either SAHA (Alexis, Grünberg, Germany) or paclitaxel (Sigma), 1/10 volume of Alamar Blue (Biosource, Solingen, Germany) solution was added and cells incubated at 37°C for an additional 3 hours. The absorbance of the wells was measured at 560/595 nm using a Wallac Victor (Perkin Elmer, Rodgau-Jügesheim, Germany) fluorometer. Results are expressed as a percentage of relative cell numbers of control cells.
Caspase-3 activity was measured 24 hours after treatment with drugs using the synthetic fluorogenic substrates Ac-DEVD-AFC (Bachem, Heidelberg, Germany). Cells were lysed in 10 mM Tris-HCl, 10 mM NaH2PO4/NaHPO4 (pH 7.5), 130 mM NaCl, 1% Triton-X-100, and 10 mM Na4P2O7 and then incubated with 20 mM Hepes (pH 7.5), 10% glycerol, 2 mM DTT and 25 μg/ml Ac-DEVD-AFC at 37°C for 2 hours. The release of trifluoromethylcoumarin (AFC) was analyzed on a Wallac Victor fluorometer using an excitation/emission wavelength of 390/510 nm. Relative caspase activities were calculated as a ratio of emission of treated cells to untreated cells.
Cytofluorometric analysis of cell death
To determine cell death, cells were harvested after a 72-h cultivation in the presence of drugs, followed by a 5-min incubation in 2 μg/ml propidium iodide (PI) (Sigma) in PBS at 4°C in the dark. PI uptake was assessed by flow cytometry analysis on a Becton Dickinson (Heidelberg, Germany) FACSCalibur using CellQuest software. 10,000 cells were analyzed in each sample; data were gated to exclude debris. Cyclosporine A (CsA; Alexis) was applied 1 hour before treatment with SAHA or paclitaxel, respectively.
Western blot analysis
Cell were lysed on ice for 15 minutes in 40 mM Tris-HCl (pH 7.4), 150 mM NaCl, 1% Triton X-100, 0.5% sodium deoxycholate, and 0.1% SDS supplemented with a protease inhibitor cocktail (Roche) followed by brief sonification. Protein concentration was assayed using bicinchoninic acid (Pierce, Rockford, IL, USA) according to the manufacturer's instructions. For immunoblotting, 30 μg of total cellular protein per lane were separated by standard SDS-PAGE on 15% gels and electrophoretically transferred to PVDF membranes (Millipore, Eschborn, Germany). After blocking in PBS containing 5% dry milk and 0.05% Tween 20, acetylated histone H3 was immunodetected rabbit anti-acetylated histone H3 (dilution 1:10,000; Upstate Biotechnology, Lake Placid, NY, USA) polyclonal antibodies. Peroxidase-conjugated goat anti-rabbit IgGs (dilution 1:12,500; Dianova, Hamburg, Germany) followed by enhanced chemiluminescence (Amersham Biosciences, Freiburg, Germany) were used for detection.
Comparison of the cytotoxic activities of SAHA and paclitaxel on ovarian cancer cells
To compare the potential activities of SAHA and paclitaxel against ovarian carcinoma cells ex vivo, we performed cytotoxicity assays with cell isolates from five patients with ovarian cancer. Four of the five ascites samples were obtained from untreated patients, one had been treated with a single dose of carboplatin/paclitaxel (ASC-OC-4). As shown in Fig 1B, SAHA evoked a dose-dependent cytotoxic effect in all five isolates. A 72-h exposure to 20 μM SAHA resulted in 21% (ASC-OC-1) to 63% (ASC-OC-4) cell killing. In contrast, four of the five isolates were resistant to paclitaxel (i.e., <10% cell death at 300 nM paclitaxel for 72 hours). Only isolate ASC-OC-4 was susceptible to this agent, with 21% cell killing observed at 72 hours by 300 nM of paclitaxel. These ex vivo observations were in part reflected by the clinical outcome of the chemotherapy: the four patients who had been chemotherapeutically naive at the time of ascites fluid removal were subsequently treated with six cycles of a paclitaxel/carboplatin combination therapy (paclitaxel at a dose of 175 mg/m2 and carboplatin at area under the concentration-time curve of 5 mg/ml/min); in two of them (ASC-OC-1 and -3), no sign of response to treatment was noted.
Comparison of the caspase-3-activating potencies of SAHA and paclitaxel
Assessment of the cytotoxic effects of the combination of SAHA and paclitaxel on ovarian cancer cells
Comparison of SAHA and paclitaxel to induce cell death in drug-resistant ovarian cancer cells
SAHA treatment leads to histone hyperacetylation in ovarian cancer cells
To the best of our knowledge, this is the first study that systematically compares an HDI and a conventional chemotherapeutic agent for their treatment efficacy in patient-derived cancer cells. HDIs hold promise as a powerful new generation of anticancer drugs. Numerous in vitro and animal studies have demonstrated that they can induce differentiation and apoptosis, inhibit cell proliferation, and exert immune stimulatory and antiangiogenic activities [reviewed in [7, 8, 10, 29]]. HDIs have also been shown to enhance the antitumour efficiency of other therapeutic regimens, such as ionizing radiation or chemotherapy. In addition, early-phase clinical trials indicate that HDIs have anticancer activity in a variety of solid and haematological malignancies. However, despite all these studies supporting the development of HDIs for clinical use, no superiority of these agents over conventional antineoplastic agents has yet been directly proven. Here we present evidence that SAHA might be more effective than paclitaxel in the treatment of ovarian cancer.
In order to establish the doses of SAHA and paclitaxel that would induce comparable cell killing in ovarian cancer cells, we initially monitored the cytotoxic activity of these compounds in three ovarian cancer cell lines. SAHA at concentrations of 1 to 20 μM was found to be as efficient in eliciting cell death as paclitaxel at concentrations of 3 to 300 nM. The killing efficiency of the latter was observed to saturate at 100 to 300 nM. This observation is in concordance with findings in clinical studies, in which paclitaxel did not seem to show dose-related efficacy in patients with ovarian cancer . In the patient-derived ovarian cancer cells, SAHA and paclitaxel were of very different effectiveness: while all five isolates responded to SAHA, four of them were unresponsive to paclitaxel. This observation made ex vivo had a correlative in vivo: two patients were resistant to paclitaxel/carboplatin treatment. However, the number of patient samples used was rather small; thus, this study should not be generalised without additional analyses. The doses of SAHA required to induce cell death in the patient-derived cells were relatively high (5–20 μM); these concentrations would be difficult to achieve in patients without severe toxic side effects [16, 18]. Yet, this limitation may be overcome by intraperitoneal administration of SAHA allowing to increase the dose without increasing systemic adverse side effects. An advantage of intraperitoneal chemotherapy in the treatment of ovarian cancer has already been demonstrated in clinical trials [31, 32, 33]. Since HDIs have been shown to cooperate with other treatment regimen in exerting antitumour effects , we also assessed whether SAHA would enhance the cytotoxic activity of paclitaxel in ovarian cancer cells. Yet, no more than additive effects were seen with this combination treatment. However, this observation is consistent with recent studies, which show that pretreatment with HDIs can enhance the cytotoxicity of DNA-targeting agents such as etoposide, but not that of drugs which do not target the DNA, like the antimetabolite 5-fluorouracil or the microtubule-active vincristine [34, 35].
Treatment failure in ovarian cancer therapy is largely due to chemotherapy resistance . One hallmark of chemoresistance is the overexpression of the Pgp drug efflux pump, which confers resistance to a variety of drugs including the taxanes . Here, we have demonstrated that Pgp-overexpressing 2780AD cells are indeed fully resistant to paclitaxel but sensitive to SAHA. This is consistent with previous findings in which SAHA was shown to induce cell death in Pgp-expressing T-cell leukaemia and colon carcinoma cells [36, 37]. So, our data on ovarian cancer cells further substantiate that SAHA is capable of killing cancer cells irrespective of their Pgp status. However, although Pgp expression correlates to chemoresistance in vitro, its in vivo significance in ovarian cancer is unclear . But as histone hypoacetylation is involved in the silencing of a number of chemotherapeutic sensitivity genes, a concerted reexpression of such genes – as accomplished by SAHA as well as other HDIs – holds promise to overcome resistance .
The importance of caspases for SAHA-  as well as for paclitaxel-induced cell death is a controversial issue. Some reports point to a critical role of caspases for SAHA-mediated cell death [35, 40, 41], whereas others suggest a caspase-independent mechanism [37, 42]. Likewise, paclitaxel-triggered cell death has been reported to proceed in a caspase-dependent [43, 44] or -independent [45, 46] manner. Here, in using the activation of caspase-3 as a measure of cytotoxic responsiveness, we do not wish to imply that caspase-3 activation would be a necessary prerequisite for SAHA- or paclitaxel-induced cell death. Clearly, the sheer activation of a caspase does not necessarily implicate its requirement for cell death. As a matter of fact, we did not observe a strict correlation between cytotoxic response and caspase-3 activation, especially in the cell lines: for example, while SAHA and paclitaxel induced comparable cytotoxicity in OVCAR-3 and SK-OV-3 cells, SAHA provoked a much higher increase in caspase-3 activity in these cell lines. Nevertheless, the caspase-3 activities observed in the patient-derived cancer cells corroborate the data obtained by Alamar Blue assay: caspase-3 activity was induced by SAHA in all five isolates, but in only two of them by paclitaxel.
In conclusion, we have shown that SAHA is able to kill paclitaxel-resistant ovarian cancer cells from patients. Since SAHA induced cell death ex vivo, it might be a promising agent for ovarian cancer therapy in vivo. However, such conclusion should be taken cum grano salis due to the small number of patient samples analysed in our study. Nonetheless, as two of the patients showed no response to paclitaxel/carboplatin treatment, it is tempting to speculate that these patients might have benefited from treatment with SAHA.
We thank Andrea Plath for excellent technical assistance.
- 1.Ries LAG, Eisner MP, Kosary CL, Hankey BF, Miller BA, Clegg L, Mariotto A, Feuer EJ, Edwards BK, (eds): SEER Cancer Statistics Review, 1975-2002. National Cancer Institute Bethesda, MD,. 2005, http://seer.cancer.gov/csr/1975_2002/, based on November 2004 SEER data submission, posted to the SEER web site 2005: [http://seer.cancer.gov/csr/1975_2002/]
- 5.Sakamoto M, Kondo A, Kawasaki K, Goto T, Sakamoto H, Miyake K, Koyamatsu Y, Akiya T, Iwabuchi H, Muroya T, Ochiai K, Tanaka T, Kikuchi Y, Tenjin Y: Analysis of gene expression profiles associated with cisplatin resistance in human ovarian cancer cell lines and tissues using cDNA microarray. Hum Cell. 2001, 14: 305-315.PubMedGoogle Scholar
- 11.Butler LM, Agus DB, Scher HI, Higgins B, Rose A, Cordon-Cardo C, Thaler HT, Rifkind RA, Marks PA, Richon VM: Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res. 2000, 60: 5165-5170.PubMedGoogle Scholar
- 12.He LZ, Tolentino T, Grayson P, Zhong S, Warrell RPJ, Rifkind RA, Marks PA, Richon VM, Pandolfi PP: Histone deacetylase inhibitors induce remission in transgenic models of therapy-resistant acute promyelocytic leukemia. J Clin Invest. 2001, 108: 1321-1330. 10.1172/JCI200111537.CrossRefPubMedPubMedCentralGoogle Scholar
- 14.Sandor V, Bakke S, Robey RW, Kang MH, Blagosklonny MV, Bender J, Brooks R, Piekarz RL, Tucker E, Figg WD, Chan KK, Goldspiel B, Fojo AT, Balcerzak SP, Bates SE: Phase I trial of the histone deacetylase inhibitor, depsipeptide (FR901228, NSC 630176), in patients with refractory neoplasms. Clin Cancer Res. 2002, 8: 718-728.PubMedGoogle Scholar
- 15.Gore SD, Weng LJ, Figg WD, Zhai S, Donehower RC, Dover G, Grever MR, Griffin C, Grochow LB, Hawkins A, Burks K, Zabelena Y, Miller CB: Impact of prolonged infusions of the putative differentiating agent sodium phenylbutyrate on myelodysplastic syndromes and acute myeloid leukemia. Clin Cancer Res. 2002, 8: 963-970.PubMedGoogle Scholar
- 16.Kelly WK, Richon VM, O'Connor O, Curley T, MacGregor-Curtelli B, Tong W, Klang M, Schwartz L, Richardson S, Rosa E, Drobnjak M, Cordon-Cordo C, Chiao JH, Rifkind R, Marks PA, Scher H: Phase I clinical trial of histone deacetylase inhibitor: suberoylanilide hydroxamic acid administered intravenously. Clin Cancer Res. 2003, 9: 3578-3588.PubMedGoogle Scholar
- 17.Ryan QC, Headlee D, Acharya M, Sparreboom A, Trepel JB, Ye J, Figg WD, Hwang K, Chung EJ, Murgo A, Melillo G, Elsayed Y, Monga M, Kalnitskiy M, Zwiebel J, Sausville EA: Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma. J Clin Oncol. 2005, 23: 3912-3922. 10.1200/JCO.2005.02.188.CrossRefPubMedGoogle Scholar
- 18.Kelly WK, O'Connor OA, Krug LM, Chiao JH, Heaney M, Curley T, MacGregore-Cortelli B, Tong W, Secrist JP, Schwartz L, Richardson S, Chu E, Olgac S, Marks PA, Scher H, Richon VM: Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer. J Clin Oncol. 2005, 23: 3923-3931. 10.1200/JCO.2005.14.167.CrossRefPubMedPubMedCentralGoogle Scholar
- 22.Strait KA, Warnick CT, Ford CD, Dabbas B, Hammond EH, Ilstrup SJ: Histone deacetylase inhibitors induce G2-checkpoint arrest and apoptosis in cisplatinum-resistant ovarian cancer cells associated with overexpression of the Bcl-2-related protein Bad. Mol Cancer Ther. 2005, 4: 603-611. 10.1158/1535-7163.MCT-04-0107.CrossRefPubMedGoogle Scholar
- 24.Saito A, Yamashita T, Mariko Y, Nosaka Y, Tsuchiya K, Ando T, Suzuki T, Tsuruo T, Nakanishi O: A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors. Proc Natl Acad Sci U S A. 1999, 96: 4592-4597. 10.1073/pnas.96.8.4592.CrossRefPubMedPubMedCentralGoogle Scholar
- 30.Bolis G, Scarfone G, Polverino G, Raspagliesi F, Tateo S, Richiardi G, Melpignano M, Franchi M, Mangili G, Presti M, Villa A, Conta E, Guarnerio P, Cipriani S, Parazzini F: Paclitaxel 175 or 225 mg per meters squared with carboplatin in advanced ovarian cancer: a randomized trial. J Clin Oncol. 2004, 22: 686-690. 10.1200/JCO.2004.03.017.CrossRefPubMedGoogle Scholar
- 31.Alberts DS, Liu PY, Hannigan EV, O'Toole R, Williams SD, Young JA, Franklin EW, Clarke-Pearson DL, Malviya VK, DuBeshter B: Intraperitoneal cisplatin plus intravenous cyclophosphamide versus intravenous cisplatin plus intravenous cyclophosphamide for stage III ovarian cancer. N Engl J Med. 1996, 335: 1950-1955. 10.1056/NEJM199612263352603.CrossRefPubMedGoogle Scholar
- 32.Markman M, Bundy BN, Alberts DS, Fowler JM, Clark-Pearson DL, Carson LF, Wadler S, Sickel J: Phase III trial of standard-dose intravenous cisplatin plus paclitaxel versus moderately high-dose carboplatin followed by intravenous paclitaxel and intraperitoneal cisplatin in small-volume stage III ovarian carcinoma: an intergroup study of the Gynecologic Oncology Group, Southwestern Oncology Group, and Eastern Cooperative Oncology Group. J Clin Oncol. 2001, 19: 1001-1007.PubMedGoogle Scholar
- 40.Henderson C, Mizzau M, Paroni G, Maestro R, Schneider C, Brancolini C: Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors trichostatin-A (TSA) and suberoylanilide hydroxamic acid (SAHA). J Biol Chem. 2003, 278: 12579-12589. 10.1074/jbc.M213093200.CrossRefPubMedGoogle Scholar
- 42.Ruefli AA, Ausserlechner MJ, Bernhard D, Sutton VR, Tainton KM, Kofler R, Smyth MJ, Johnstone RW: The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species. Proc Natl Acad Sci U S A. 2001, 98: 10833-10838. 10.1073/pnas.191208598.CrossRefPubMedPubMedCentralGoogle Scholar
- 44.Friedrich K, Wieder T, Von Haefen C, Radetzki S, Janicke R, Schulze-Osthoff K, Dorken B, Daniel PT: Overexpression of caspase-3 restores sensitivity for drug-induced apoptosis in breast cancer cell lines with acquired drug resistance. Oncogene. 2001, 20: 2749-2760. 10.1038/sj.onc.1204342.CrossRefPubMedGoogle Scholar
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