Volume 130, Issue 5 pp. 1021-1028
Cancer Cell Biology

Oct1 regulates cell growth of LNCaP cells and is a prognostic factor for prostate cancer

Daisuke Obinata

Daisuke Obinata

Department of Anti-Aging Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Department of Urology, Nihon University School of Medicine, Bunkyo-ku, Tokyo, Japan

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Ken-ichi Takayama

Ken-ichi Takayama

Department of Anti-Aging Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Bunkyo-ku, Tokyo, Japan

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Tomohiko Urano

Tomohiko Urano

Department of Anti-Aging Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Bunkyo-ku, Tokyo, Japan

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Taro Murata

Taro Murata

Department of Anti-Aging Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Department of Urology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

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Jinpei Kumagai

Jinpei Kumagai

Department of Urology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

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Tetsuya Fujimura

Tetsuya Fujimura

Department of Urology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

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Kazuhiro Ikeda

Kazuhiro Ikeda

Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Bunkyo-ku, Tokyo, Japan

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Kuniko Horie-Inoue

Kuniko Horie-Inoue

Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Bunkyo-ku, Tokyo, Japan

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Yukio Homma

Yukio Homma

Department of Urology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

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Yasuyoshi Ouchi

Yasuyoshi Ouchi

Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

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Satoru Takahashi

Satoru Takahashi

Department of Urology, Nihon University School of Medicine, Bunkyo-ku, Tokyo, Japan

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Satoshi Inoue

Corresponding Author

Satoshi Inoue

Department of Anti-Aging Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan

Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Bunkyo-ku, Tokyo, Japan

Tel.: 81-3-5800-8834, Fax: 81-3-5800-9126

Department of Anti-Aging Medicine, Graduate School of Medicine, University of Tokyo, Bunkyo-ku, Tokyo 113-8655, JapanSearch for more papers by this author
First published: 08 March 2011
Citations: 51

Abstract

The androgen receptor (AR) plays a critical role in the development and the progression of prostate cancer. Alterations in the expression of AR coregulators lead to AR hypersensitivity, which is one of the mechanisms underlying the progression of prostate cancer into a castrate-resistant state. Octamer transcription factor 1 (Oct1) is a ubiquitous member of the POU-homeodomain family that functions as a coregulator of AR. In our study, the contribution of Oct1 to prostate cancer development was examined. Immunocytochemistry analysis showed that Oct1 is expressed in the nuclei of LNCaP cells. siRNA-mediated silencing of Oct1 expression inhibited LNCaP cell proliferation. Immunohistochemical analysis of Oct1 expression in tumor specimens obtained from 102 patients with prostate cancer showed a positive correlation of Oct1 immunoreactivity with a high Gleason score and AR immunoreactivity (p = 0.0042 and p < 0.0001, respectively). Moreover, patients with high immunoreactivity of Oct1 showed a low cancer-specific survival rate, and those patients with high immunoreactivities of both Oct1 and AR exhibited poorer cancer-specific prognosis. Multivariate hazard analysis revealed a significant correlation between high Oct1 immunoreactivity and poor cancer-specific survival (p = 0.012). These results demonstrate that Oct1 can be a prognostic factor in prostate cancer as a coregulator of AR and may lead to the development of a new therapeutic intervention for prostate cancer.

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