Regulation of multidrug resistance by microRNAs in anti-cancer therapy

被引:162
作者
An, Xin [1 ,2 ]
Sarmiento, Cesar [2 ]
Tan, Tao [2 ]
Zhu, Hua [2 ]
机构
[1] Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou 510060, Guangdong, Peoples R China
[2] Ohio State Univ, Dept Surg, Davis Heart & Lung Res Inst, Wexner Med Ctr, Columbus, OH 43210 USA
基金
中国国家自然科学基金;
关键词
Multidrug resistance; miRNA; Cancer; Therapy; Autophagy; Redox Homeostasis; GLUTATHIONE-S-TRANSFERASE; BREAST-CANCER CELLS; HUMAN HEPATOCELLULAR-CARCINOMA; P53 PROTEIN EXPRESSION; DRUG-RESISTANCE; GASTRIC-CANCER; DOWN-REGULATION; COLORECTAL-CANCER; MDR1/P-GLYCOPROTEIN EXPRESSION; CISPLATIN RESISTANCE;
D O I
10.1016/j.apsb.2016.09.002
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Multidrug resistance (MDR) remains a major clinical obstacle to successful cancer treatment. Although diverse mechanisms of MDR have been well elucidated, such as dysregulation of drugs transporters, defects of apoptosis and autophagy machinery, alterations of drug metabolism and drug targets, disrupti on of redox homeostasis, the exact mechanisms of MDR in a specific cancer patient and the cross-talk among these different mechanisms and how they are regulated are poorly understood. MicroRNAs (miRNAs) are a new class of small noncoding RNAs that could control the global activity of the cell by post-transcriptionally regulating a large variety of target genes and proteins expression. Accumulating evidence shows that miRNAs play a key regulatory role in MDR through modulating various drug resistant mechanisms mentioned above, thereby holding much promise for developing novel and more effective individualized therapies for cancer treatment. This review summarizes the various MDR mechanisms and mainly focuses on the role of miRNAs in regulating MDR in cancer treatment. (C) 2017 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:38 / 51
页数:14
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