腺病毒介导的RNA干扰ERCC1基因表达对卵巢癌顺铂化疗的增敏作用

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Abstract Objective To study the enhancement of sensitivity of DDP in ovary carcinoma by expressions of adenovirus-mediated RNA that interferes with ERCC1 genes.Methods SKOV3 cells were infected by direct infection methods and with recombinant adenovirus. Taipan blue dye, MTT, Hoechst staining and flow cytometer were used to draw SKOV3 cell growth curves and doubling time. DDP’sIC50, apoptosis morphology and the cell cycle distribution of ovary carcinoma cell line SKOV3 before and after the recombinant adenovirus infection were detected.Results (1) There was a linear positive correlation between the concentration of DDP and the cell inhibition rate of SKOV3, and the correlation coefficient r=0.9905(P<0.05), while DDP’sIC50 was (7.76±0.37)μg/ml.Ad-HTERT-ERCC1-siRNA had some inhibitory effect on SKOV3.(2)Drug sensitivity test showed that apoptosis of SKOV3 cells increased with the infectious viral titer and the concentration of DDP, and that cell survival rate significantly decreased in a dose-dependent manner.(3)As the infectious viral titer and the concentration of DDP were increased, the cell apoptosis was significantly elevated.(4)The recombinant adenovirus expression vector could increase S stage and cell apoptosis, but decrease G1 stage predominantly.Conclusions The recombinant adenovirus expression vector can effectively enhance DDP’s sensitivity to SKOV3 by inducing the apoptosis of tumor cells and regulating the cycle distribution of tumor cells.

Key words： ovarian carcinoma ERCC1 gene RNA interference recombinant adenovirus expression vector

Received: 05 January 2018

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R731.31

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	Articles by authors
	TIAN Lina
	QU Quanxin
	SHENG Xiaobin
	XU Fuqiang

Cite this article:

TIAN Lina,QU Quanxin,SHENG Xiaobin等. Effect of expressions of adenovirus-mediated RNA interfering with ERCC1 genes on sensitivity of DDP in ovary carcinoma[J]. Med. J. Chin. Peop. Armed Poli. Forc., 2018, 29(4): 361-366.

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http://journal08.magtechjournal.com/Jwk_wjyx/EN/ OR http://journal08.magtechjournal.com/Jwk_wjyx/EN/Y2018/V29/I4/361

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