Effect of plasmid-mediated stable interferon-γ expression on proliferation and cell death in the SKOV-3 human ovarian cancer cell line

被引:5
|
作者
Lv, Huiming [1 ]
Zhang, Huiya [1 ]
Wu, Jiaolei [1 ]
Guan, Yongmei [1 ]
机构
[1] Harbin Med Coll, Affiliated Hosp 1, Reprod Unit, Harbin, Peoples R China
关键词
Interferon-gamma; immunotherapy; ovarian carcinoma vaccine; plasmid vector; proliferation; IFN-GAMMA; CARCINOMA-CELLS; 1ST-LINE TREATMENT; INDUCED APOPTOSIS; GENE-TRANSFER; IN-VITRO; THERAPY; GROWTH; CARBOPLATIN; ACTIVATION;
D O I
10.3109/08923973.2010.543685
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: High interferon-gamma (IFN-gamma) expression in tumors has been reported to be a favorable prognostic marker. Continuous exposure of ovarian cancer cells to IFN-gamma was previously shown to result in significant growth inhibition and apoptosis. Our goal in this study was to evaluate the effect of plasmid-mediated stable IFN-gamma expression on the SKOV-3 human ovarian carcinoma cell line. Methods: SKOV-3 cells were stably transfected with the pEGFP-IFN-gamma plasmid. IFN-gamma mRNA was detected by RT-PCR and IFN-gamma protein expression was measured by ELISA. Proliferation and cell death in transfected SKOV-3 cells were measured by methyl-thiazolyl tetrazolium (MTT) assay and Hoechst 33258 staining, respectively and compared with untransfected and empty vector-transfected cells. Results: pEGFP-IFN-gamma SKOV-3 cells efficiently expressed and secreted IFN-gamma. They exhibited significantly decreased cellular proliferation when compared with control untransfected or empty vector-transfected cells (P < 0.05). The mode of cell death was primarily apoptosis. Conclusions: Stable expression of IFN-gamma significantly inhibits the proliferation of ovarian carcinoma cells and has the potential to be used in clinical applications to treat ovarian carcinoma in the future.
引用
收藏
页码:498 / 503
页数:6
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