MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer

被引:94
作者
Su, Jiaojiao [1 ]
Liang, Hongwei [2 ]
Yao, Weiyan [3 ]
Wang, Nan [2 ]
Zhang, Suyang [2 ]
Yan, Xin [4 ,5 ]
Feng, Hui [1 ]
Pang, Wenjing [3 ]
Wang, Yanbo [2 ]
Wang, Xueliang [2 ]
Fu, Zhen [2 ]
Liu, Yanqing [2 ]
Zhao, Chihao [2 ]
Zhang, Junfeng [2 ]
Zhang, Chen-Yu [2 ]
Zen, Ke [2 ]
Chen, Xi [2 ]
Wang, Yalei [1 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Gastroenterol, Hefei 230022, Anhui, Peoples R China
[2] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Jiangsu Engn Res Ctr MicroRNA Biol & Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Gastroenterol, Shanghai 200025, Peoples R China
[4] Nanjing Univ, Sch Med, Drum Tower Hosp, Ctr Comprehens Canc, Nanjing 210008, Jiangsu, Peoples R China
[5] Nanjing Univ, Clin Canc Inst, Nanjing 210008, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MICRORNA SIGNATURES; I RECEPTOR; GROWTH; METASTASIS; EXPRESSION; PREDICTION; ONCOMIRS;
D O I
10.1371/journal.pone.0114420
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Insulin-like growth factor 1 receptor (IGF1R) is a transmembrane receptor that is activated by insulin-like growth factor 1 (IGF-1) and by a related hormone called IGF-2. It belongs to the large class of tyrosine kinase receptors and plays an important role in colorectal cancer etiology and progression. In this study, we used bioinformatic analyses to search for miRNAs that potentially target IGF1R. We identified specific target sites for miR-143 and miR-145 (miR-143/145) in the 3'-untranslated region (3 '-UTR) of the IGF1R gene. These miRNAs are members of a cluster of miRNAs that have been reported to exhibit tumor suppressor activity. Consistent with the bioinformatic analyses, we identified an inverse correlation between miR-143/145 levels and IGF1R protein levels in colorectal cancer tissues. By overexpressing miR-143/145 in Caco2, HT29 and SW480 colorectal cancer cells, we experimentally validated that miR-143/145 directly recognizes the 3'-UTR of the IGF1R transcript and regulates IGF1R expression. Furthermore, the biological consequences of the targeting of IGF1R by miR-143/145 were examined by cell proliferation assays in vitro. We demonstrated that the repression of IGF1R by miR-143/145 suppressed the proliferation of Caco2 cells. Taken together, our findings provide evidence for a role of the miR-143/145 cluster as a tumor suppressor in colorectal cancer through the inhibition of IGF1R translation.
引用
收藏
页数:15
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