| Literature DB >> 27915273 |
Taketoshi Nara1, Shintaro Narita2,3, Huang Mingguo1,3, Toshiaki Yoshioka4, Atsushi Koizumi1,3, Kazuyuki Numakura1, Hiroshi Tsuruta1, Atsushi Maeno1, Mitsuru Saito1, Takamitsu Inoue1,3, Norihiko Tsuchiya5, Shigeru Satoh1, Tomonori Habuchi1,3.
Abstract
Recent evidence suggests that a high-fat diet (HFD) plays an important role in prostate carcinogenesis; however, underlying mechanisms largely remain unknown. Here, we investigated microRNA (miRNA) expression changes in murine prostate cancer (PCa) xenografts using two different diets: HFD and control diet. We then assessed the roles and targets of altered miRNAs in HFD-induced PCa progression. We identified 38 up- and 21 downregulated miRNAs in xenografts under HFD conditions using the miRCURY LNA™ microRNA array. The differences in 10 candidate miRNAs were validated using quantitative RT-PCR. We focused on miR-130a because the expression levels were significantly lower in the three PCa cell lines in comparison with benign prostate PINT1B cells. PCa cells cultured in a medium containing HFD mouse serum were associated with significantly higher cell proliferation rates and lower miR-130a expression levels. Further, miR-130a modulated MET expression in PCa cells, and MET was overexpressed in in vitro and in vivo HFD-induced PCa progression models. Moreover, ectopic miR-130a downregulated AR in LNCaP cells and DICER1 in PC-3 and DU145 cells, respectively. In human tissues, as elucidated using laser capture microdissection, the mean miR-130a expression level in cancer epithelium was significantly lower than that in normal epithelium. Furthermore, cytoplasmic MET in PCa tissues was overexpressed in patients with higher body mass index. In conclusion, a substantial number of miRNAs was altered in HFD-induced PCa growth. Specifically, miR-130a was attenuated in HFD-induced PCa progression with MET overexpression. miRNAs thus have implications in the mechanism, prevention and treatment of HFD-induced PCa progression.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27915273 DOI: 10.1093/carcin/bgw108
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944