Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Department of Medical Biophysics, University of Toronto, Toronto, Canada.
Protein Cell. 2021 Jan;12(1):29-38. doi: 10.1007/s13238-020-00786-8. Epub 2020 Sep 18.
Prostate cancer is the most commonly diagnosed non-cutaneous cancers in North American men. While androgen deprivation has remained as the cornerstone of prostate cancer treatment, resistance ensues leading to lethal disease. Forkhead box A1 (FOXA1) encodes a pioneer factor that induces open chromatin conformation to allow the binding of other transcription factors. Through direct interactions with the Androgen Receptor (AR), FOXA1 helps to shape AR signaling that drives the growth and survival of normal prostate and prostate cancer cells. FOXA1 also possesses an AR-independent role of regulating epithelial-to-mesenchymal transition (EMT). In prostate cancer, mutations converge onto the coding sequence and cis-regulatory elements (CREs) of FOXA1, leading to functional alterations. In addition, FOXA1 activity in prostate cancer can be modulated post-translationally through various mechanisms such as LSD1-mediated protein demethylation. In this review, we describe the latest discoveries related to the function and regulation of FOXA1 in prostate cancer, pointing to their relevance to guide future clinical interventions.
前列腺癌是北美男性最常见的非皮肤癌。虽然雄激素剥夺疗法一直是前列腺癌治疗的基石,但随之而来的是耐药性,导致致命的疾病。叉头框转录因子 A1(FOXA1)编码一种先驱因子,可诱导开放染色质构象,允许其他转录因子结合。通过与雄激素受体(AR)的直接相互作用,FOXA1 有助于塑造 AR 信号,从而驱动正常前列腺和前列腺癌细胞的生长和存活。FOXA1 还具有独立于 AR 的调节上皮-间充质转化(EMT)的作用。在前列腺癌中,突变集中在 FOXA1 的编码序列和顺式调控元件(CREs)上,导致功能改变。此外,前列腺癌细胞中的 FOXA1 活性可以通过各种机制进行翻译后修饰,如 LSD1 介导的蛋白质去甲基化。在这篇综述中,我们描述了与 FOXA1 在前列腺癌中的功能和调节相关的最新发现,指出它们与指导未来临床干预的相关性。