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TRAF6 regulates proliferation of stromal cells in the transition and peripheral zones of benign prostatic hyperplasia via Akt/mTOR signaling
Author(s) -
Shi YunFeng,
Yu DianJun,
Jiang ChenYi,
Wang XingJie,
Zhu YiPing,
Zhao RuiZhe,
Lv Zhong,
Sun XiaoWen
Publication year - 2018
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.23456
Subject(s) - stromal cell , pi3k/akt/mtor pathway , cancer research , protein kinase b , transfection , downregulation and upregulation , hyperplasia , cell growth , biology , cell culture , chemistry , medicine , endocrinology , microbiology and biotechnology , phosphorylation , signal transduction , biochemistry , genetics , gene
Background Increased prostatic smooth muscle tone and hyperplastic growth contribute to urethral obstruction and voiding symptoms in benign prostatic hyperplasia (BPH). It has been suggested that different proliferative potential of stromal cells between transition zone (TZ) and adjoining regions of the prostate plays a significant role in the development of BPH. However, the molecular mechanisms of this hyperplastic process remain unclear. We found tumor necrosis factor receptor‐associated factor 6 (TRAF6) highly expressed in TZ stromal cells compared to peripheral zone (PZ) stromal cells by gene array analyzes. Therefore, we aim to study the potential mechanisms of stromal TRAF6 in promoting BPH progression. Methods Stromal cells obtained from BPH‐derived primary cultures. The TRAF6‐siRNA vector were constructed and transfected into cultured human BPH primary TZ stromal cells, and TRAF6‐overexpressing vector were constructed and transfected into cultured human BPH primary PZ stromal cells. Stromal cells were recombined with BPH‐1 cells then subcutaneously inoculated into the kidney capsule of male nude mice. Cell proliferation was evaluated by CCK‐8 assay. Multiple proteins in the Akt/mTOR pathway were assessed using western blot. Results TRAF6 levels were increased in TZ stroma compared with PZ stroma of BPH. The in vitro cell culture and in vivo cell recombination revealed that selective downregulation of TRAF6 in TZ stromal cells led to suppression of the proliferation, while upregulation of TRAF6 in PZ stromal cells enhanced the proliferation. We found that the Phosphorylation and Ubiquitination of Akt as well as the Phosphorylation of mTOR, P70 S6K were decreased when TRAF6 was downregulated in primary cultured TZ stromal cells of BPH. Conclusions TRAF6 can promote the proliferation of stromal cells of BPH via Akt/mTOR signaling. Our results may make stromal TRAF6 responsible for zonal characteristic of BPH and as a promising therapeutic strategy for BPH treatment.

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