Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Biochemistry and Molecular Biology Graduate Program, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, MN 55905, USA.
Asian J Androl. 2019 May-Jun;21(3):241-248. doi: 10.4103/aja.aja_41_18.
Therapy resistance is a significant challenge for prostate cancer treatment in clinic. Although targeted therapies such as androgen deprivation and androgen receptor (AR) inhibition are effective initially, tumor cells eventually evade these strategies through multiple mechanisms. Lineage reprogramming in response to hormone therapy represents a key mechanism that is increasingly observed. The studies in this area have revealed specific combinations of alterations present in adenocarcinomas that provide cells with the ability to transdifferentiate and perpetuate AR-independent tumor growth after androgen-based therapies. Interestingly, several master regulators have been identified that drive plasticity, some of which also play key roles during development and differentiation of the cell lineages in the normal prostate. Thus, further study of each AR-independent tumor type and understanding underlying mechanisms are warranted to develop combinational therapies that combat lineage plasticity in prostate cancer.
治疗抵抗是临床前列腺癌治疗的重大挑战。尽管靶向治疗如雄激素剥夺和雄激素受体 (AR) 抑制在初期是有效的,但肿瘤细胞最终会通过多种机制逃避这些策略。针对激素治疗的谱系重编程是一个越来越被关注的关键机制。该领域的研究揭示了在腺癌中存在的特定改变组合,这些改变赋予了细胞转分化的能力,并在基于雄激素的治疗后维持 AR 非依赖性肿瘤生长。有趣的是,已经鉴定出几个驱动可塑性的主要调控因子,其中一些在正常前列腺细胞谱系的发育和分化过程中也发挥着关键作用。因此,有必要进一步研究每种 AR 非依赖性肿瘤类型并了解潜在机制,以开发联合治疗方法来对抗前列腺癌中的谱系可塑性。