miR-181b functions as an oncomiR in colorectal cancer by targeting PDCD4.
- Author:
Yanqing LIU
1
;
UZAIR-UR-REHMAN
1
;
Yu GUO
1
;
Hongwei LIANG
1
;
Rongjie CHENG
1
;
Fei YANG
1
;
Yeting HONG
1
;
Chihao ZHAO
1
;
Minghui LIU
1
;
Mengchao YU
1
;
Xinyan ZHOU
1
;
Kai YIN
2
;
Jiangning CHEN
1
;
Junfeng ZHANG
1
;
Chen-Yu ZHANG
3
;
Feng ZHI
4
;
Xi CHEN
5
Author Information
1. State Key Laboratory of Pharmaceutical Biotechnology, Collaborative Innovation Center of Chemistry for Life Sciences, Jiangsu Engineering Research Center for MicroRNA Biology and Biotechnology, NJU Advanced Institute for Life Sciences (NAILS), School of Life Sciences, Nanjing University, 163 Xianlin Road, Nanjing, 210046, China.
2. Department of Gastrointestinal Surgery, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, 321 Zhongshan Road, Nanjing, 210008, China.
3. State Key Laboratory of Pharmaceutical Biotechnology, Collaborative Innovation Center of Chemistry for Life Sciences, Jiangsu Engineering Research Center for MicroRNA Biology and Biotechnology, NJU Advanced Institute for Life Sciences (NAILS), School of Life Sciences, Nanjing University, 163 Xianlin Road, Nanjing, 210046, China. cyzhang@nju.edu.cn.
4. Modern Medical Research Center, Third Affiliated Hospital of Soochow University, 185 Juqian Road, Changzhou, 213003, China. danielzhif@163.com.
5. State Key Laboratory of Pharmaceutical Biotechnology, Collaborative Innovation Center of Chemistry for Life Sciences, Jiangsu Engineering Research Center for MicroRNA Biology and Biotechnology, NJU Advanced Institute for Life Sciences (NAILS), School of Life Sciences, Nanjing University, 163 Xianlin Road, Nanjing, 210046, China. xichen@nju.edu.cn.
- Publication Type:Journal Article
- Keywords:
PDCD4;
colorectal cancer;
miR-181b;
microRNA
- MeSH:
Animals;
Apoptosis Regulatory Proteins;
genetics;
metabolism;
Caco-2 Cells;
Cell Proliferation;
Colorectal Neoplasms;
genetics;
metabolism;
pathology;
Heterografts;
Humans;
Male;
Mice;
Mice, Nude;
Mice, SCID;
MicroRNAs;
genetics;
metabolism;
Neoplasm Proteins;
genetics;
metabolism;
Neoplasm Transplantation;
RNA, Neoplasm;
genetics;
metabolism;
RNA-Binding Proteins;
genetics;
metabolism
- From:
Protein & Cell
2016;7(10):722-734
- CountryChina
- Language:English
-
Abstract:
Programmed cell death 4 (PDCD4) is a RNA-binding protein that acts as a tumor suppressor in many cancer types, including colorectal cancer (CRC). During CRC carcinogenesis, PDCD4 protein levels remarkably decrease, but the underlying molecular mechanism for decreased PDCD4 expression is not fully understood. In this study, we performed bioinformatics analysis to identify miRNAs that potentially target PDCD4. We demonstrated miR-181b as a direct regulator of PDCD4. We further showed that activation of IL6/STAT3 signaling pathway increased miR-181b expression and consequently resulted in downregulation of PDCD4 in CRC cells. In addition, we investigated the biological effects of PDCD4 inhibition by miR-181b both in vitro and in vivo and found that miR-181b could promote cell proliferation and migration and suppress apoptosis in CRC cells and accelerate tumor growth in xenograft mice, potentially through targeting PDCD4. Taken together, this study highlights an oncomiR role for miR-181b in regulating PDCD4 in CRC and suggests that miR-181b may be a novel molecular therapeutic target for CRC.
