蛋白激酶A与雄激素信号通路的串扰

Manisha Dagar, G. Bhattacharjee
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引用次数: 2

摘要

蛋白激酶是在蛋白质上添加磷酸基团以改变其功能的酶。这些蛋白调节信号转导通路,在细胞周期、细胞信号传导、蛋白质和酶调节等许多生物过程中起重要作用。有518种蛋白激酶,分为7个主要家族。蛋白激酶A (PKA)是AGC蛋白激酶家族的一员。它通过G蛋白偶联受体(GPCR)的激活而激活,在包括雄激素信号在内的许多细胞通路中起重要作用。类固醇激素如雄激素主要通过基因组途径发挥作用,与细胞质雄激素受体(AR)结合并启动靶基因转录的变化。雄激素也通过非基因组途径发挥作用,该途径是由膜受体介导的快速途径。它通过激活细胞信号转导通路如PKA、蛋白激酶C和丝裂原活化激酶来表现其作用,不涉及转录。在这篇综述中,我们分析了雄激素信号通路和PKA之间的相互作用,并强调了这些通路如何相互补充和增强功能。PKA在核AR的完全激活中起重要作用,而PKA又可被雄激素激活。这两种通路之间复杂的相互作用在前列腺癌(PCa)的发生和发展中起着关键作用。虽然每个途径的确切作用还不完全清楚,但同时抑制这两个途径可能对PCa患者有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cross Talk between Protein Kinase A and Androgen Signaling Pathway
Protein kinases are enzymes that add phosphate group to proteins to modify their function. These proteins regulate signal transduction pathways, essential for many biological processes such as cell cycle, cell signaling, protein and enzyme regulation, etc. There are 518 protein kinases, divided in to 7 main families. Protein kinase A (PKA) is a member of AGC family of protein kinases. It is activated by activation of G protein-coupled receptors (GPCR) and plays an important role in many cellular pathways including androgen signaling. Steroid hormones such as androgens primarily function through a genomic pathway, binding to cytosolic androgen receptors (AR) and initiating changes in transcription of target genes. Androgens also functions through a non-genomic pathway which is rapid and mediated by membrane receptors. It manifests its effects by activation of cellular signal transduction pathways such as PKA, Protein kinase C, and mitogen activated kinase, and does not involve transcription. In this review, we have analyzed the interaction between androgen signaling pathways and PKA, and have highlighted how each of these pathways complements and strengthens the function of the other. PKA plays an important role in complete activation of nuclear AR and in turn PKA can be activated by androgens. The complex interaction between the two pathways plays a critical role in development and progression of prostate cancer (PCa). Though the exact role of each pathway is not completely understood yet simultaneous inhibition of both pathways could prove to be beneficial for PCa patients.
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