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[Study on the Effect of Overexpression of miR-18a on Cellular Proliferation and Migration by Targeting ATM in Human Colorectal Cancer Cells].
Liu, Ming-Jia; Chen, Li-Hong; Hu, Kai-Feng; Yang, Xiao-Long; Dong, Jing-Ying; Liu, Ji.
Affiliation
  • Liu MJ; Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Chen LH; Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Hu KF; Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Yang XL; Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Dong JY; Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.
  • Liu J; Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban ; 47(4): 451-457, 2016 Jul.
Article in Zh | MEDLINE | ID: mdl-28591941
ABSTRACT

OBJECTIVES:

To study the regulation to colon cancer cellular biological properties through miR-18a targeting ataxia-telangiectasia mutated gene (ATM).

METHODS:

A target of miR-18a was predicted by using bioinformatics tools. The miR-18a mimics and inhibitors were designed and synthesized. The expression of endogenous miR-18a in colon cancer cell line HCT116 was up-regulated or down-regulated by transfection. The effect of overexpression of miR-18a on cellular proliferation, invasion and migration via regulation of ATM gene expression was confirmed in vitro by using qRT-PCR, Western blot, MTT assay, clone forming assay and Transwell method, respectively.

RESULTS:

ATM was identified as a potential target gene of miR-18a in the bioinformatics analysis. In addition, through transient transfection leading to the overexpression of miR-18a in HCT116 cell, the expression level of ATM was decreased. Down-regulation of HCT116 cell proliferation activity while significantly reducing HCT116 cell clone forming ability, lateral migration ability and longitudinal invasion ability were observed after transfected with miR-18a mimics. All of the changes were related to the overexpression of miR-18a.

CONCLUSIONS:

miR-18a inhibited the proliferation and migration of colon cance cell HCT116 through negative regulation of ATM expression.
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Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Cell Movement / MicroRNAs / Cell Proliferation / Ataxia Telangiectasia Mutated Proteins Limits: Humans Language: Zh Journal: Sichuan Da Xue Xue Bao Yi Xue Ban Year: 2016 Type: Article Affiliation country: China
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Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Cell Movement / MicroRNAs / Cell Proliferation / Ataxia Telangiectasia Mutated Proteins Limits: Humans Language: Zh Journal: Sichuan Da Xue Xue Bao Yi Xue Ban Year: 2016 Type: Article Affiliation country: China