Redox regulation of microRNAs in cancer

被引:41
作者
Lan, Jiang [1 ,2 ,3 ]
Huang, Zhao [1 ,2 ,3 ]
Han, Junhong [1 ,2 ,3 ]
Shao, Jichun [4 ]
Huang, Canhua [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, State Key Lab Biotherapy & Canc Ctr, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Sch Basic Med Sci & Forens Med, Chengdu 610041, Sichuan, Peoples R China
[3] Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[4] China Natl Nucl Corp 416 Hosp, Chengdu Med Coll, Affiliated Hosp 2, Dept Urol, Chengdu, Sichuan, Peoples R China
关键词
ROS; Oxidative stress; Redox signaling; microRNA; Cancer; NF-KAPPA-B; OXIDATIVE STRESS; BREAST-CANCER; DOWN-REGULATION; UP-REGULATION; CELL-DEATH; C-MYC; SUPEROXIDE-DISMUTASE; TRANSCRIPTION FACTOR; LUNG TUMORIGENESIS;
D O I
10.1016/j.canlet.2018.01.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dysregulation of microRNAs (miRNAs) has long been implicated in tumorigenesis, whereas the underlying mechanisms remain largely unknown. Oxidative stress is a hallmark of cancer that involved in multiple pathophysiological processes, including the aberrant regulation of miRNAs. Compelling evidences have implied complicated interplay between reactive oxygen species (ROS) and miRNAs. Indeed, ROS induces carcinogenesis through either reducing or increasing the miRNA level, leading to the activation of oncogenes or silence of tumor suppressors, respectively. In turn, miRNAs target ROS productive genes or antioxidant responsive elements to affect cellular redox balance, which contributes to establishing a microenvironment favoring cancer cell growth and metastasis. Both miRNAs and ROS have been identified as potential biomarkers and therapeutic targets in human malignancies, and comprehensive understanding of the molecular events herein will facilitate the development of novel cancer therapeutic strategies. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:250 / 259
页数:10
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