Target Protein for Xklp2 Functions as Coactivator of Androgen Receptor and Promotes the Proliferation of Prostate Carcinoma Cells

Author:

Sun Baisheng1,Long Yin2,Xiao Ling3,Wang Jiazhi4,Yi Qian5ORCID,Tong Dali2ORCID,Li Ke2ORCID

Affiliation:

1. Emergency Department, The Fifth Medical Center of the General Hospital of the Chinese People's Liberation Army, Beijing 100071, China

2. Department of Urology, Daping Hospital, Army Medical University, Chongqing 400042, China

3. Institute of Hematopoietic Stem Cell of PLA, Department of Hematopoietic Stem Cell Transplantation, The Fifth Medical Center of the General Hospital of the Chinese People' Liberation Army, Beijing 100071, China

4. Medical Service Department of 63650 Army Hospital of the Chinese People's Liberation Army, Urumqi 841700, China

5. Emergency Department, Chongqing Traditional Chinese Medicine Hospital, Chongqing 400021, China

Abstract

The activation of the androgen receptor (AR) pathway is crucial in the progression of human prostate cancer. Results of the present study indicated that the target protein xenopus kinesin-like protein (TPX2) enhanced the transcription activation of AR and promoted the proliferation of LNCaP (ligand-dependent prostate carcinoma) cells. The protein-protein interaction between AR and TPX2 was investigated using coimmunoprecipitation assays. Results of the present study further demonstrated that TPX2 enhanced the transcription factor activation of AR and enhanced the expression levels of the downstream gene prostate-specific antigen (PSA). TPX2 did this by promoting the accumulation of AR in the nucleus and also promoting the recruitment of AR to the androgen response element, located in the promoter region of the PSA gene. Overexpression of TPX2 enhanced both the in vitro and in vivo proliferation of LNCaP cells. By revealing a novel role of TPX2 in the AR signaling pathway, the present study indicated that TPX2 may be an activator of AR and thus exhibits potential as a novel target for prostate carcinoma treatment.

Publisher

Hindawi Limited

Subject

Oncology

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