Khatiwada Prabesh, Rimal Ujjwal, Malla Mamata, Han Zhengyang, Shemshedini Lirim
Department of Biological Sciences, University of Toledo, Toledo, Ohio, USA.
Center for Translational Immunology, Columbia University, New York, NY, USA.
Endocr Oncol. 2023 Aug 29;3(1):e230010. doi: 10.1530/EO-23-0010. eCollection 2023 Jan 1.
Androgen receptor (AR) plays a vital role in the development and progression of prostate cancer from the primary stage to the usually lethal stage known as castration-resistant prostate cancer (CRPC). Constitutively active AR splice variants (AR-Vs) lacking the ligand-binding domain are partially responsible for the abnormal activation of AR and may be involved in resistance to AR-targeting drugs occurring in CRPC. There is increasing consensus on the potential of drugs targeting protein-protein interactions. Our lab has recently identified transmembrane 4 superfamily 3 (TM4SF3) as a critical interacting partner for AR and AR-V7 and mapped the minimal interaction regions. Thus, we hypothesized that these interaction domains can be used to design peptides that can disrupt the AR/TM4SF3 interaction and kill prostate cancer cells. Peptides TA1 and AT1 were designed based on the TM3SF3 or AR interaction domain, respectively. TA1 or AT1 was able to decrease AR/TM4SF3 protein interaction and protein stability. Peptide TA1 reduced the recruitment of AR and TM4SF3 to promoters of androgen-regulated genes and subsequent activation of these AR target genes. Peptides TA1 and AT1 were strongly cytotoxic to prostate cancer cells that express AR and/or AR-V7. Peptide TA1 inhibited the growth and induced apoptosis of both enzalutamide-sensitive and importantly enzalutamide-resistant prostate cancer cells. TA1 also blocked the migration and malignant transformation of prostate cancer cells. Our data clearly demonstrate that using peptides to target the important interaction AR has with TM4SF3 provides a novel method to kill enzalutamide-resistant prostate cancer cells that can potentially lead to new more effective therapy for CRPC.
雄激素受体(AR)在前列腺癌从原发阶段发展到通常致命的去势抵抗性前列腺癌(CRPC)阶段的过程中起着至关重要的作用。缺乏配体结合域的组成型活性AR剪接变体(AR-Vs)部分导致了AR的异常激活,并可能参与CRPC中对AR靶向药物的耐药性。针对蛋白质-蛋白质相互作用的药物潜力已达成越来越多的共识。我们实验室最近已确定跨膜4超家族3(TM4SF3)是AR和AR-V7的关键相互作用伙伴,并绘制了最小相互作用区域。因此,我们假设这些相互作用域可用于设计能够破坏AR/TM4SF3相互作用并杀死前列腺癌细胞的肽。肽TA1和AT1分别基于TM3SF3或AR相互作用域设计。TA1或AT1能够降低AR/TM4SF3蛋白相互作用和蛋白稳定性。肽TA1减少了AR和TM4SF3募集到雄激素调节基因的启动子以及这些AR靶基因的后续激活。肽TA1和AT1对表达AR和/或AR-V7的前列腺癌细胞具有强烈的细胞毒性。肽TA1抑制恩杂鲁胺敏感以及重要的是恩杂鲁胺耐药前列腺癌细胞的生长并诱导其凋亡。TA1还阻断了前列腺癌细胞的迁移和恶性转化。我们的数据清楚地表明,使用肽靶向AR与TM4SF3的重要相互作用提供了一种杀死恩杂鲁胺耐药前列腺癌细胞的新方法,这可能会为CRPC带来新的更有效的治疗方法。