MicroRNAs in colorectal carcinoma - from pathogenesis to therapy

被引:108
作者
Chi, Yudan [1 ]
Zhou, Dongming [1 ]
机构
[1] Chinese Acad Sci, Inst Pasteur Shanghai, Vaccine Res Ctr, Key Lab Mol Virol & Immunol, Shanghai 200031, Peoples R China
关键词
MicroRNA; Colorectal carcinoma; Pathogenesis; Diagnosis; Cancer therapy; HUMAN COLON-CANCER; P55-GAMMA REGULATORY SUBUNIT; CELL-CYCLE PROGRESSION; RECTAL-CANCER; TUMOR-GROWTH; E-CADHERIN; MESENCHYMAL TRANSITION; ULCERATIVE-COLITIS; INHIBITS MIGRATION; PROMOTES APOPTOSIS;
D O I
10.1186/s13046-016-0320-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Acting as inflammatory mediators, tumor oncogenes or suppressors, microRNAs are involved in cell survival, death, epithelial-mesenchymal transition and metastasis, etc. Investigating the communication between microRNAs and tumorigenesis is critical to our understanding of the pathogenesis of multiple disease states. Main body: Currently, colorectal carcinoma (CRC), one of the most common malignancies worldwide, has a poor prognosis due to lack of an effective therapeutic option. Increasing evidence has identified altered profiles and regulatory potential of microRNAs in conditions related to environmentally-caused colorectal inflammation and colitis-associated cancer. Many studies have shed light on a more thorough understanding of the function and distribution of microRNAs in CRC initiation and emergence. However, the molecular mechanisms by which microRNAs modulate cellular processes still need to be further elucidated and may offer a foundation for evaluating microRNA-based therapeutic potential for CRC in both animal models and clinical trials. Conclusion: In this review, the roles and mechanisms of microRNAs involved in CRC from pathogenesis to therapy are summarized and discussed, which may provide more useful hints for CRC prevention and therapy.
引用
收藏
页数:11
相关论文
共 153 条
[1]
Ahmed FE, 2012, CANCER GENOM PROTEOM, V9, P179
[2]
Ahmed Farid E., 2009, Cancer Genomics & Proteomics, V6, P281
[3]
The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[4]
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[5]
MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[6]
MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[7]
Bonfrate L, 2013, J GASTROINTEST LIVER, V22, P311
[8]
MicroRNA-143 reduces viability and increases sensitivity to 5-fluorouracil in HCT116 human colorectal cancer cells [J].
Borralho, Pedro M. ;
Kren, Betsy T. ;
Castro, Rui E. ;
da Silva, Isabel B. Moreira ;
Steer, Clifford J. ;
Rodrigues, Cecilia M. P. .
FEBS JOURNAL, 2009, 276 (22) :6689-6700
[9]
Variable β-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment [J].
Brabletz, T ;
Jung, A ;
Reu, S ;
Porzner, M ;
Hlubek, F ;
Kunz-Schughart, LA ;
Knuechel, R ;
Kirchner, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10356-10361
[10]
A microRNA miR-34a-Regulated Bimodal Switch Targets Notch in Colon Cancer Stem Cells [J].
Bu, Pengcheng ;
Chen, Kai-Yuan ;
Chen, Joyce Huan ;
Wang, Lihua ;
Walters, Jewell ;
Shin, Yong Jun ;
Goerger, Julian P. ;
Sun, Jian ;
Witherspoon, Mavee ;
Rakhilin, Nikolai ;
Li, Jiahe ;
Yang, Herman ;
Milsom, Jeff ;
Lee, Sang ;
Zipfel, Warren ;
Jin, Moonsoo M. ;
Guemues, Zeynep H. ;
Lipkin, Steven M. ;
Shen, Xiling .
CELL STEM CELL, 2013, 12 (05) :602-615