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前列腺癌干细胞动力学在耐药性演变中的作用

Prostate cancer stem cell dynamics in the evolution of drug resistance.

作者信息

Zhang Xiaoyu, Zhang Xiaoqing, Deng Xinpei, Cao Jingna, Bao Qing, Wang Huan, Chen Dong, Tang Hailin

机构信息

State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-Sen University Cancer Center, Guangzhou, China.

出版信息

Int J Surg. 2025 Jun 4. doi: 10.1097/JS9.0000000000002611.

Abstract

Prostate cancer (PCa) remains a leading cause of cancer-related mortality in men worldwide, with tumor heterogeneity, therapy resistance, and lineage plasticity posing significant clinical challenges. Androgen deprivation therapy (ADT), while initially effective, often culminates in castration-resistant prostate cancer (CRPC), may fueled by castration-resistant prostate cancer stem cells (CSCs) with adaptive self-renewal and regenerative capacities. Emerging evidence implicates prostate CSCs as pivotal contributors to tumor heterogeneity, drug resistance, and disease recurrence. These stem subpopulations exhibit intrinsic adaptability through genetic, epigenetic, and microenvironmental reprogramming, enabling survival under androgen-deprived conditions and fostering clonal diversification. This review synthesizes current knowledge on the identity, regulation, and functional dynamics of prostate stem cells, emphasizing their role in shaping the tumor ecosystem. By dissecting the genetic drivers, epigenetic alteration and crosstalk with microenvironment, this review underscores critical triggers on prostate CSCs determination and differentiation. Additionally, we discuss emerging strategies to target prostate CSCs-specific vulnerabilities, including molecular drivers of stemness and plasticity, to improve therapeutic outcomes for advanced prostate malignancies. This synthesis underscores the critical need to unravel prostate stem cells biology for developing precision therapies against prostate CSCs-driven adaptation in prostate diseases.

摘要

前列腺癌(PCa)仍然是全球男性癌症相关死亡的主要原因,肿瘤异质性、治疗耐药性和谱系可塑性带来了重大的临床挑战。雄激素剥夺疗法(ADT)虽然最初有效,但往往最终会发展为去势抵抗性前列腺癌(CRPC),这可能是由具有适应性自我更新和再生能力的去势抵抗性前列腺癌干细胞(CSCs)所推动的。新出现的证据表明,前列腺CSCs是肿瘤异质性、耐药性和疾病复发的关键因素。这些干细胞亚群通过基因、表观遗传和微环境重编程表现出内在适应性,使其能够在雄激素剥夺条件下存活并促进克隆多样化。本综述综合了关于前列腺干细胞的身份、调控和功能动态的现有知识,强调了它们在塑造肿瘤生态系统中的作用。通过剖析基因驱动因素、表观遗传改变以及与微环境的相互作用,本综述强调了前列腺CSCs决定和分化的关键触发因素。此外,我们还讨论了针对前列腺CSCs特异性弱点的新兴策略,包括干性和可塑性的分子驱动因素,以改善晚期前列腺恶性肿瘤的治疗效果。这一综述强调了深入了解前列腺干细胞生物学对于开发针对前列腺CSCs驱动的前列腺疾病适应性的精准疗法的迫切需求。

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