文献类型：期刊文献

英文题名：miR-297 modulates multidrug resistance in human colorectal carcinoma by down-regulating MRP-2

作者：Xu, Ke[3,4];Liang, Xin[3,4];Shen, Ke[3,4];Cui, Daling[3,4];Zheng, Yuanhong[3,4];Xu, Jianhua[1,2];Fan, Zhongze[1,2];Qiu, Yanyan[1,2];Li, Qi[1,2];Ni, Lei[5];Liu, Jianwen[3,4]

机构：[1]Shanghai Univ Tradit Chinese Med, Dept Clin Oncol, Putuo Hosp, Shanghai 200062, Peoples R China;[2]Shanghai Univ Tradit Chinese Med, Inst Canc, Shanghai 200062, Peoples R China;[3]E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Sch Pharm, Shanghai 200237, Peoples R China;[4]E China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, Shanghai 200237, Peoples R China;[5]Shanghai Jiao Tong Univ, Dept Resp, Ruijin Hosp, Sch Med, Shanghai 200025, Peoples R China

年份：2012

卷号：446

起止页码：291

外文期刊名：BIOCHEMICAL JOURNAL

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000308767500013)】；

基金：This work was supported by the Shanghai Committee of Science and Technology [grant numbers 11DZ2260600 and 10ZR14274001 and the Ministry of Education of China.

语种：英文

外文关键词：colorectal carcinoma; microRNA (miRNA); microRNA array; multidrug resistance (MDR); multictrug resistance-associated protein 2 (MRP-2)

摘要：Colorectal carcinoma is a frequent cause of cancer-related death in men and women. miRNAs (microRNAs) are endogenous small non-coding RNAs that regulate gene expression negatively at the post-transcriptional level. In the present study we investigated the possible role of microRNAs in the development of MDR (multidrug resistance) in colorectal carcinoma cells. We analysed miRNA expression levels between MDR colorectal carcinoma cell line HCT116/L-OHP cells and their parent cell line HCT116 using a miRNA microarray. miR-297 showed lower expression in HCT116/L-OHP cells compared with its parental cells. MRP2 (MDR-associated protein 2) is an important MDR protein in platinum-drug-resistance cells and is a predicted target of miR297. Additionally miR-297 was down-regulated in a panel of human colorectal carcinoma tissues and negatively correlated with expression levels of MRP-2. Furthermore, we found that ectopic expression of miR-297 in MDR colorectal carcinoma cells reduced MRP-2 protein level and sensitized these cells to anticancer drugs in vitro and in vivo. Taken together, our findings suggest that miR-297 could play a role in the development of MDR in colorectal carcinoma cells, at least in part by modulation of MRP-2.