MicroRNA-modulated autophagic signaling networks in cancer

被引:143
|
作者
Fu, Lei-Lei [1 ,2 ]
Wen, Xin [1 ,2 ]
Bao, Jin-ku [1 ,2 ]
Liu, Bo [1 ,2 ]
机构
[1] Sichuan Univ, State Key Lab Biotherapy, W China Hosp, Sch Life Sci, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Ctr Canc, W China Hosp, Sch Life Sci, Chengdu 610041, Peoples R China
来源
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY | 2012年 / 44卷 / 05期
关键词
MicroRNA (miRNA); Cancer; Autophagy; Oncogene; Tumor suppressor; PATHWAYS; APOPTOSIS; TARGETS; DISEASE;
D O I
10.1016/j.biocel.2012.02.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are small, non-coding endogenous RNAs 22 nucleotides (nt) in length that may play the essential roles for regulation of programed cell death, referring to apoptosis and autophagy. Of note, autophagy is an evolutionarily conserved, multi-step lysosomal degradation process in which a cell degrades long-lived proteins and damaged organelles. Accumulating evidence has recently revealed that miRNAs can modulate the autophagic pathways in many pathological processes, most notably cancer. In this review, we focus on highlighting the dual functions of miRNAs as either oncogenes (e.g., miRNA-183, miRNA-376b, miRNA-106a, miRNA-221/222, miRNA-31 and miRNA-34c) or tumor suppressors (e.g., miRNA-30a, miRNA-101 and miRNA-9*) via mediating several autophagic signaling pathways in cancer pathogenesis. Taken together, these findings may uncover the regulatory mechanisms of oncogenic and tumor suppressive miRNAs in autophagy, which would provide a better understanding of miRNA-modulated autophagic signaling networks for future cancer therapeutics. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:733 / 736
页数:4
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