| Literature DB >> 25117438 |
Saya Ito1, Takashi Ueda2, Akihisa Ueno2, Hideo Nakagawa2, Hidefumi Taniguchi2, Naruhiro Kayukawa2, Tsuneharu Miki2.
Abstract
To uncover the mechanism by which human prostate cancer progresses, we performed a genetic screen for regulators of human prostate cancer progression using the Drosophila accessory gland, a functional homolog of the mammalian prostate. Cell growth and migration of secondary cells in the adult male accessory gland were found to be regulated by paired, N-cadherin, and E-cadherin, which are Drosophila homologues of regulators of human prostate cancer progression. Using this screening system, we also identified three genes that promoted growth and migration of secondary cells in the accessory gland. The human homologues of these candidate genes - MRGBP, CNPY2, and MEP1A - were found to be expressed in human prostate cancer model cells and to promote replication and invasiveness in these cells. These findings suggest that the development of the Drosophila accessory gland and human prostate cancer cell growth and invasion are partly regulated through a common mechanism. The screening system using the Drosophila accessory gland can be a useful tool for uncovering the mechanisms of human prostate cancer progression.Entities:
Keywords: Accessory gland; Drosophila; Prostate cancer
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Year: 2014 PMID: 25117438 DOI: 10.1016/j.bbrc.2014.08.015
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575