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2016 Fiscal Year Final Research Report

Development of "Ubiquitin" -targeted Prostate cancer treatment

Research Project

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Project/Area Number 26462392
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Urology
Research InstitutionHokkaido University

Principal Investigator

Miyajima Naoto  北海道大学, 大学病院, 助教 (40581111)

Project Period (FY) 2014-04-01 – 2017-03-31
Keywordsユビキチン / 前立腺癌
Outline of Final Research Achievements

We previously found that the putative E3 ubiquitin ligase TRIM68, which is preferentially expressed in prostate cancer cells, interacts with the AR (androgen receptor) and enhances transcriptional activity of the AR in the presence of androgen. We also found that TRIM68 functionally interacts with TIP60 and p300, which act as coactivators of the AR, and synergizes in transactivation of the AR.
To reveal how the ubiquitination contribute to the AR function, we used molecular biology approaches such as immunoprecipitation assay, western blotting and Ubiquitination assay.Using several AR co-repressors and TRIM68 specific antibody, we performed immunoprecipitation and ubiquitination assay to identify the substrate of TRIM68 ubiquitin ligase. Unfortunately, we could not identify it, but these results indicate that TRIM68 functions as a cofactor for AR-mediated transcription and is likely to be a novel diagnostic tool and a potentially therapeutic target for prostate cancer.

Free Research Field

泌尿器科癌

URL: 

Published: 2018-03-22  

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