MicroRNA-183 in Cancer Progression

被引:58
作者
Cao, Dingren [1 ]
Di, Min [2 ]
Liang, Jingjie [1 ]
Shi, Shuang [1 ]
Tan, Qiang [1 ]
Wang, Zhengguang [1 ]
机构
[1] Zhejiang Univ, Coll Anim Sci, 866 Yuhangtang Rd, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Coll Med, Sir Run Shaw Hosp, Hangzhou 310058, Peoples R China
关键词
microRNA-183; cancer progression; EMT; metastasis; microangiogenesis; PROMOTES CELL-PROLIFERATION; EPITHELIAL-MESENCHYMAL TRANSITION; HUMAN BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; TUMOR-SUPPRESSOR; GASTRIC-CANCER; INHIBITS APOPTOSIS; MIR-183; EXPRESSION; REGULATING PDCD4; TARGETING MMP-9;
D O I
10.7150/jca.39044
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNA-183(miR-183) is abnormally expressed in many kinds of tumors. It participates in the initiation and development of tumors. There are many pathways regulate the expression of miR-183. The action mechanism of miR-183 in cancer is very extensive, and contradictory conclusions are often drawn. It was upregulated in 18 kinds of cancer, downregulated in 6 kinds of cancer. In addition, there are seven types of cancer, both upregulated and downregulated reports can be found. Evidence showed that miR-183 can not only directly play the role of oncogene or antioncogene, but also regulate the expression of other oncogene or antioncogene in different cancer types. In this review, we discuss the regulator of miR-183 and summarized the expression of miR-183 in different cancers. We also counted the target genes of miR-183 and the functional roles they play. Furthermore, we focused on the roles of miR-183 in cell migration, cell invasion, epithelial-mesenchymal transition (EMT) and microangiogenesis, which play the most important roles in cancer processes. It sheds light on the likely reasons why miR-183 plays different roles in various cancers. In addition, miR-183 and its downstream effectors have the potential to be promising prognostic markers and therapeutic targets in cancer.
引用
收藏
页码:1315 / 1324
页数:10
相关论文
共 113 条
[31]   New microRNAs from mouse and human [J].
Lagos-Quintana, M ;
Rauhut, R ;
Meyer, J ;
Borkhardt, A ;
Tuschl, T .
RNA, 2003, 9 (02) :175-179
[32]   ZEB1-repressed microRNAs inhibit autocrine signaling that promotes vascular mimicry of breast cancer cells [J].
Langer, E. M. ;
Kendsersky, N. D. ;
Daniel, C. J. ;
Kuziel, G. M. ;
Pelz, C. ;
Murphy, K. M. ;
Capecchi, M. R. ;
Sears, R. C. .
ONCOGENE, 2018, 37 (08) :1005-1019
[33]   miR-183 in Prostate Cancer Cells Positively Regulates Synthesis and Serum Levels of Prostate-specific Antigen [J].
Larne, Olivia ;
Ostling, Paivi ;
Haflidadottir, Benedikta S. ;
Hagman, Zandra ;
Aakula, Anna ;
Kohonen, Pekka ;
Kallioniemi, Olli ;
Edsjo, Anders ;
Bjartell, Anders ;
Lilja, Hans ;
Lundwall, Ake ;
Ceder, Yvonne .
EUROPEAN UROLOGY, 2015, 68 (04) :581-588
[34]   Wnt/β-Catenin activates MiR-183/96/182 expression in hepatocellular carcinoma that promotes cell invasion [J].
Leung, Wilson K. C. ;
He, Mian ;
Chan, Anthony W. H. ;
Law, Priscilla T. Y. ;
Wong, Nathalie .
CANCER LETTERS, 2015, 362 (01) :97-105
[35]   MicroRNA-183 Functions As an Oncogene by Regulating PDCD4 in Gastric Cancer [J].
Li, Chenglong ;
Deng, Li ;
Zhi, Qiaoming ;
Meng, Qingyou ;
Qian, Aimin ;
Sang, Hongfei ;
Li, Xiaoqiang ;
Xia, Jiazeng .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2016, 16 (04) :447-455
[36]   Targeting of Integrin β1 and Kinesin 2α by MicroRNA 183 [J].
Li, Guorong ;
Luna, Coralia ;
Qiu, Jianming ;
Epstein, David L. ;
Gonzalez, Pedro .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (08) :5461-5471
[37]   MicroRNA-183 Family Members Regulate Sensorineural Fates in the Inner Ear [J].
Li, Haiqiong ;
Kloosterman, Wigard ;
Fekete, Donna M. .
JOURNAL OF NEUROSCIENCE, 2010, 30 (09) :3254-3263
[38]  
Li J, 2010, BMC EVOL BIOL, V10, DOI [10.1186/1471-2148-10-68, 10.1186/1471-2407-10-354]
[39]   Tiam1, negatively regulated by miR-22, miR-183 and miR-31, is involved in migration, invasion and viability of ovarian cancer cells [J].
Li, Jun ;
Liang, Shanhui ;
Jin, Hongyan ;
Xu, Congjian ;
Ma, Duan ;
Lu, Xin .
ONCOLOGY REPORTS, 2012, 27 (06) :1835-1842
[40]   MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration [J].
Li, Pei ;
Sheng, Cheng ;
Huang, Lingling ;
Zhang, Hui ;
Huang, Lihua ;
Cheng, Zeneng ;
Zhu, Qubo .
BREAST CANCER RESEARCH, 2014, 16 (06)