| Literature DB >> 28000854 |
Tsuyoshi Hata1, Yukako Mokutani2, Hidekazu Takahashi1, Akira Inoue1, Koji Munakata1, Kazuya Nagata3, Naotsugu Haraguchi1, Junichi Nishimura1, Taishi Hata1, Chu Matsuda1, Kohei Murata4, Tsunekazu Mizushima1, Yuichiro Doki1, Masaki Mori1, Hirofumi Yamamoto1.
Abstract
Recent studies have shown that microRNAs (miRNAs) are involved in the progression of colorectal cancer (CRC). The aim of this study is to identify a novel miRNA that especially relates to liver metastasis and to explore the underlying mechanism. Differentially expressed miRNAs were analyzed using microarray, in primary CRC tumors without metastasis (n=16), those with liver metastasis (n=12), and liver metastatic lesions (n=8). We found that miR-487b level decreased in liver metastatic lesions, and qRT-PCR confirmed the results in the validating cohort (n=134). Survival analysis indicated that high expression of miR-487b was associated with better prognosis. In vitro studies were also performed to investigate the functional significance of miR-487b in human CRC cell lines. miR-487b showed an inhibitory effect on cell proliferation and invasion of CRC cells. miR-487b downregulated KRAS and inhibited its downstream signal pathways, and the luciferase reporter assay revealed that miR-487b directly targeted LRP6, a receptor for WNT/β-catenin signaling. These findings showed that decrease in miR-487b was related with liver metastasis. Our data suggest a possibility that miR-487b may suppress metastasis of CRC progression through inhibition of KRAS.Entities:
Mesh:
Substances:
Year: 2016 PMID: 28000854 DOI: 10.3892/ijo.2016.3813
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650