| Literature DB >> 27035873 |
Shao-Mei Zhou1, Fang Zhang1, Xue-Bin Chen1, Cao-Ming Jun1, Xin Jing1, Deng-Xiong Wei1, Yang Xia1, Yu-Bai Zhou1, Xiang-Qian Xiao1, Run-Qing Jia1, Jing-Tao Li1, Wang Sheng1, Yi Zeng1.
Abstract
MicroRNAs are highly conserved non-coding RNAs that regulate gene expression at the post-transcriptional level, and play pivotal roles in cancer development and progression. miR-100 has been reported to be significantly downregulated in a variety of cancers, including esophageal cancer. However, the role of miR-100 in human esophageal cancer has not been fully elucidated. We demonstrated that overexpression of miR-100 in esophageal cancer cells markedly inhibited cell proliferation, migration and invasion as well as tumor growth. We subsequently showed that CXCR7 is a direct target gene of miR-100. Our results indicated that miR-100 plays a tumor-suppressor role in esophageal cancer and suggest its potential application for esophageal cancer treatment.Entities:
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Year: 2016 PMID: 27035873 DOI: 10.3892/or.2016.4701
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906