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前列腺中雄激素受体与过氧化物酶体增殖物激活受体γ信号通路之间的相互作用

Crosstalk between the Androgen Receptor and PPAR Gamma Signaling Pathways in the Prostate.

作者信息

Olokpa Emuejevoke, Moss Patrice E, Stewart LaMonica V

机构信息

Department of Biochemistry and Cancer Biology, Meharry Medical College, Nashville, TN 37208, USA.

出版信息

PPAR Res. 2017;2017:9456020. doi: 10.1155/2017/9456020. Epub 2017 Oct 18.

Abstract

Nuclear receptors are a superfamily of ligand-activated transcription factors that play critical roles in the regulation of normal biological processes and several disease states. Of the nuclear receptors expressed within the prostate, the androgen receptor (AR) promotes the differentiation of prostatic epithelial cells and stimulates production of enzymes needed for liquefaction of semen. Multiple forms of AR also promote the growth of both early and late stage prostate cancers. As a result, drugs that target the AR signaling pathway are routinely used to treat patients with advanced forms of prostate cancer. Data also suggest that a second member of the nuclear receptor superfamily, the peroxisome proliferator activated receptor gamma (PPAR), is a tumor suppressor that regulates growth of normal prostate and prostate cancers. Recent studies indicate there is a bidirectional interaction between AR and PPAR, with each receptor influencing the expression and/or activity of the other within prostatic tissues. In this review, we examine how AR and PPAR each regulate the growth and development of normal prostatic epithelial cells and prostate cancers. We also discuss interactions between the AR and PPAR signaling pathways and how those interactions may influence prostate biology.

摘要

核受体是一类配体激活的转录因子超家族,在正常生物学过程和多种疾病状态的调节中发挥关键作用。在前列腺中表达的核受体中,雄激素受体(AR)促进前列腺上皮细胞的分化,并刺激精液液化所需酶的产生。多种形式的AR还促进早期和晚期前列腺癌的生长。因此,靶向AR信号通路的药物通常用于治疗晚期前列腺癌患者。数据还表明,核受体超家族的另一个成员,过氧化物酶体增殖物激活受体γ(PPAR),是一种调节正常前列腺和前列腺癌生长的肿瘤抑制因子。最近的研究表明,AR和PPAR之间存在双向相互作用,每种受体在前列腺组织中都会影响另一种受体的表达和/或活性。在这篇综述中,我们研究了AR和PPAR如何各自调节正常前列腺上皮细胞和前列腺癌的生长与发育。我们还讨论了AR和PPAR信号通路之间的相互作用,以及这些相互作用如何影响前列腺生物学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2117/5664321/225fcf03fa2e/PPAR2017-9456020.001.jpg

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