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The role of mesenchymal stem cells in promoting the transformation of androgen-dependent human prostate cancer cells into androgen-independent manner

机译:间充质干细胞在促进雄激素依赖性人前列腺癌细胞转化成雄激素独立的方式的作用

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Mesenchymal stem cells (MSCs) play an important role in the development of human prostate cancer (PCa). However, the role of MSCs in the transformation of androgen-dependent human PCa cells into androgen-independent manner has been poorly understood. In this study, we investigated the underlying mechanism of MSCs in promoting PCa cells from androgen-dependent into androgen-independent manner. Firstly, we demonstrated that MSCs could affect the transformation of androgen-dependent human PCa cells into androgen-independent manner in vivo and in vitro . Then we found a substantial expression of TGF-β in MSCs. TGF-β blockade could significantly inhibit the promotive function of MSCs in PCa cells. Besides that, we also demonstrated androgen might inhibit the expression of TGF-β in MSCs. Furthermore, we found that either overexpression of SSEA-4 or the number of SSEA-4 positive MSCs in PCa tissues was associated with a shorter cancer-free survival interval (CFSI) and a worse overall survival (OS). Our results suggest that androgen blockade treatment in clinical PCa therapy may elicit the expression of TGF-β in MSCs, which will result in the transformation of androgen-dependent human PCa cells into androgen-independent manner.
机译:间充质干细胞(MSCs)在人类前列腺癌(PCA)的发展中起重要作用。然而,MSCs在雄激素依赖性人PCA细胞转化到雄激素独立的方式的作用已经理解。在这项研究中,我们研究了MSCs在促进雄激素的PCA细胞依赖于雄激素依赖性方式的潜在机制。首先,我们证明MSCs可以影响雄激素依赖性人PCA细胞的转化为体内和体外雄激素的方式。然后我们发现MSCs中的TGF-β大量表达。 TGF-β阻滞可显着抑制MSCs在PCA细胞中的促进功能。除此之外,我们还证明雄激素可能抑制MSCs中TGF-β的表达。此外,我们发现SSEA-4的过表达或PCA组织中的SSEA-4阳性MSCs的数量与较短的无癌症存活间隔(CFSI)和更差的整体存活(OS)相关。我们的研究结果表明,临床PCA治疗中的雄激素阻断治疗可能引起MSC中TGF-β的表达,这将导致雄激素依赖性人PCA细胞转化为雄激素独立的方式。

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