c-Myc silencing impedes cell proliferation and enhances cytotoxicity of cisplatin in non-small cell lung cancer

被引:0
|
作者
Liu, Xiang [1 ]
Wu, Chen [2 ]
Wu, Yanhu [1 ]
Tang, Yihu [1 ]
Du, Jin [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Cardiothorac Surg, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Soochow Univ, Affiliated Hosp 3, Dept Oncol & Tumor Biol Treatment, Changzhou 213003, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2016年 / 9卷 / 09期
关键词
c-Myc; non-small cell lung cancer; cell proliferation; cisplatin; THERAPY; ANGIOGENESIS; EXPRESSION; GROWTH; GENE; P53;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated the expression of c-Myc in non-small cell lung cancer (NSCLC) tissues and explored the effect of c-Myc silencing on cell proliferation and cisplatin cytotoxicity. mRNA expression levels of c-Myc in 84 NSCLC tissue samples and corresponding para-cancerous tissues were detected by real-time PCR. c-Myc small interfering RNA (siRNA) was transfected into NSCLC H1299 cells by Lipofectamine 2000. Real-time PCR was carried out to validate the transfection efficiency. Cell Counting Kit-8 was used to evaluate cell proliferation. Cisplatin toxicity experiments using CCK-8 assays showed cytotoxicity of cisplatin plus c-Myc gene silencing in NSCLC cells. The c-Myc mRNA level in NSCLC tissues was significantly higher than that in corresponding para-cancerous tissues (P < 0.05). c-Myc siRNA was successfully transfected into H1299 cells. The proliferation rates of H1299 cells after c-Myc silencing at 24, 48 and 72 h were lower than those of control groups (P < 0.05). The combination of c-Myc silencing and cisplatin had the most cytotoxic effect on H1299 cells compared with individual and control groups (P < 0.05). c-Myc may act as an oncogene in NSCLC and could be a potential target for NSCLC gene therapy.
引用
收藏
页码:9199 / 9205
页数:7
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