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Down-Regulation of microRNA-132 is Associated with Poor Prognosis of Colorectal Cancer

Authors :
Hirofumi Yamamoto
Ichiro Takemasa
Koji Munakata
Naotsugu Haraguchi
Daisuke Okuzaki
Mamoru Uemura
Tsunekazu Mizushima
Masaki Mori
Taishi Hata
Hidekazu Takahashi
Junichi Nishimura
Kohei Murata
Yuichiro Doki
Yukako Mokutani
Source :
Annals of Surgical Oncology
Publication Year :
2016
Publisher :
Springer Science and Business Media LLC, 2016.

Abstract

Background Given the role of microRNA in colorectal cancer (CRC) progression, we explored the association between microRNA (miRNA) expression and CRC-related prognosis. Methods Three types of tissue samples (primary CRC lesions without liver metastasis, primary lesions with liver metastasis, and liver metastatic tissues) were used for miRNA profiling to identify differentially expressed miRNA. Quantitative real-time PCR was used to examine miRNA expression in CRC cells and in tumor tissues. Results MiR-132 was significantly down-regulated in primary CRC tissues with liver metastasis and liver metastatic lesions compared to primary lesions without liver metastasis. Multivariate analysis for overall survival indicated that low miR-132 expression was an independent prognostic factor for CRC patients (overall survival P = 0.040, disease-free survival P = 0.015). Ectopic expression of miR-132 significantly inhibited cell proliferation and cell invasion. The luciferase reporter assay revealed that anoctamin 1 (ANO1) was a direct target of miR-132. Kaplan–Meier survival curves showed that high ANO1 expression was a significant prognostic factor for overall survival of patients with CRC (P = 0.0344). Conclusions Down-regulation of miR-132 is associated with poor prognosis in CRC. ANO1 could be one of the crucial targets of miR-132 in CRC. Electronic supplementary material The online version of this article (doi:10.1245/s10434-016-5133-3) contains supplementary material, which is available to authorized users.

Details

ISSN :
15344681 and 10689265
Volume :
23
Database :
OpenAIRE
Journal :
Annals of Surgical Oncology
Accession number :
edsair.doi.dedup.....565cb89acd66a75a38a8a48156ce947a
Full Text :
https://doi.org/10.1245/s10434-016-5133-3