Role of microRNAs in translation regulation and cancer

被引:62
作者
Stefania Oliveto [1 ]
Marilena Mancino [1 ]
Nicola Manfrini [1 ]
Stefano Biffo [1 ,2 ]
机构
[1] INGM, National Institute of Molecular Genetics “Romeo ed Enrica Invernizzi”
[2] Department of Biosciences, University of Milan
关键词
MicroRNA; Translation; Cancer; OncomiR; Tumor suppressor;
D O I
暂无
中图分类号
R73-3 [肿瘤学实验研究];
学科分类号
100214 ;
摘要
MicroRNAs(miRNAs) are pervasively expressed and regulate most biological functions. They function by modulating transcriptional and translational programs and therefore they orchestrate both physiological and pathological processes, such as development, cell differentiation, proliferation, apoptosis and tumor growth. miRNAs work as small guide molecules in RNA silencing, by negatively regulating the expression of several genes both at mRNA and protein level, by degrading their mRNA target and/or by silencing translation. One of the most recent advances in the field is the comprehension of their role in oncogenesis. The number of miRNA genes is increasing and an alteration in the level of miRNAs is involved in the initiation, progression and metastases formation of several tumors. Some tumor types show a distinct miRNA signature that distinguishes them from normal tissues and from other cancer types. Genetic and biochemical evidence supports the essential role of miRNAs in tumor development. Although the abnormal expression of miRNAs in cancer cells is a widely accepted phenomenon, the cause of this dysregulation is still unknown. Here, we discuss the biogenesis of miRNAs, focusing on the mechanisms by which they regulate protein synthesis. In addition we debate on their role in cancer, highlighting their potential to become therapeutic targets.
引用
收藏
页码:45 / 56
页数:12
相关论文
共 44 条
[1]   Exosome and Exosomal MicroRNA: Trafficking, Sorting, and Function [J].
Jian Zhang ;
Sha Li ;
Lu Li ;
Meng Li ;
Chongye Guo ;
Jun Yao ;
Shuangli Mi .
Genomics,Proteomics & Bioinformatics, 2015, (01) :17-24
[2]  
mi RISC and the CCR 4– NOT complex silence mRNA targets independently of 43S ribosomal scanning[J] . Duygu Kuzuo?lu‐?ztürk,Dipankar Bhandari,Eric Huntzinger,Maria Fauser,Sigrun Helms,Elisa Izaurralde.The EMBO Journal . 2016 (11)
[3]  
Extracellular Vesicles in Cancer: Exosomes, Microvesicles and the Emerging Role of Large Oncosomes[J] . Valentina R. Minciacchi,Michael R. Freeman,Dolores Di Vizio.Seminars in Cell and Developmental Biology . 2015
[4]  
A LINE‐1–encoded reverse transcriptase–dependent regulatory mechanism is active in embryogenesis and tumorigenesis[J] . Corrado Spadafora.Ann. N.Y. Acad. Sci. . 2015 (1)
[5]  
Alternative mRNA transcription, processing, and translation: insights from RNA sequencing[J] . Eleonora de Klerk,Peter A.C. ‘t Hoen.Trends in Genetics . 2015 (3)
[6]  
eIF6 anti-association activity is required for ribosome biogenesis, translational control and tumor progression[J] . Daniela Brina,Annarita Miluzio,Sara Ricciardi,Stefano Biffo.BBA - Gene Regulatory Mechanisms . 2014
[7]   MicroRNAs Trigger Dissociation of eIF4AI and eIF4AII from Target mRNAs in Humans [J].
Fukao, Akira ;
Mishima, Yuichiro ;
Takizawa, Naoki ;
Oka, Shigenori ;
Imataka, Hiroaki ;
Pelletier, Jerry ;
Sonenberg, Nahum ;
Thoma, Christian ;
Fujiwara, Toshinobu .
MOLECULAR CELL, 2014, 56 (01) :79-89
[8]  
MicroRNA binding sites in the coding region of mRNAs: Extending the repertoire of post‐transcriptional gene regulation[J] . Anneke Brümmer,Jean Hausser.BioEssays . 2014 (6)
[9]   Cancer-Secreted miR-105 Destroys Vascular Endothelial Barriers to Promote Metastasis [J].
Zhou, Weiying ;
Fong, Miranda Y. ;
Min, Yongfen ;
Somlo, George ;
Liu, Liang ;
Palomares, Melanie R. ;
Yu, Yang ;
Chow, Amy ;
O'Connor, Sean Timothy Francis ;
Chin, Andrew R. ;
Yen, Yun ;
Wang, Yafan ;
Marcusson, Eric G. ;
Chu, Peiguo ;
Wu, Jun ;
Wu, Xiwei ;
Li, Arthur Xuejun ;
Li, Zhuo ;
Gao, Hanlin ;
Ren, Xiubao ;
Boldin, Mark P. ;
Lin, Pengnian Charles ;
Wang, Shizhen Emily .
CANCER CELL, 2014, 25 (04) :501-515
[10]   MicroRNA Directly Enhances Mitochondrial Translation during Muscle Differentiation [J].
Zhang, Xiaorong ;
Zuo, Xinxin ;
Yang, Bo ;
Li, Zongran ;
Xue, Yuanchao ;
Zhou, Yu ;
Huang, Jie ;
Zhao, Xiaolu ;
Zhou, Jie ;
Yan, Yun ;
Zhang, Huiqiong ;
Guo, Peipei ;
Sun, Hui ;
Guo, Lin ;
Zhang, Yi ;
Fu, Xiang-Dong .
CELL, 2014, 158 (03) :607-619