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去势抵抗性前列腺癌中恩杂鲁胺耐药的机制及克服耐药的治疗策略。

Mechanisms of enzalutamide resistance in castration-resistant prostate cancer and therapeutic strategies to overcome it.

作者信息

Wang Yuanyuan, Chen Jiyuan, Wu Zhengjie, Ding Weihong, Gao Shen, Gao Yuan, Xu Chuanliang

机构信息

Department of Clinical Pharmacy and Pharmaceutical Management, School of Pharmacy, Fudan University, Shanghai, China.

Department of Urology, Changhai Hospital, Second Military Medical University, Shanghai, China.

出版信息

Br J Pharmacol. 2021 Jan;178(2):239-261. doi: 10.1111/bph.15300. Epub 2020 Dec 14.

Abstract

Prostate cancer is the second most common malignancy in men and androgen deprivation therapy is the first-line therapy. However, most cases will eventually develop castration-resistant prostate cancer after androgen deprivation therapy treatment. Enzalutamide is a second-generation androgen receptor antagonist approved by the Food and Drug Administration to treat patients with castration-resistant prostate cancer. Unfortunately, patients receiving enzalutamide treatment will ultimately develop resistance via various complicated mechanisms. This review examines the emerging information on these resistance mechanisms, including androgen receptor-related signalling pathways, glucocorticoid receptor-related pathways and metabolic effects. Notably, lineage plasticity and phenotype switching, gene polymorphisms and the relationship between microRNAs and drug resistance are addressed. Furthermore, potential therapeutic strategies for enzalutamide-resistant castration-resistant prostate cancer treatment are suggested, which can help discover more effective and specific regimens to overcome enzalutamide resistance.

摘要

前列腺癌是男性中第二常见的恶性肿瘤,雄激素剥夺疗法是一线治疗方法。然而,大多数病例在接受雄激素剥夺治疗后最终会发展为去势抵抗性前列腺癌。恩杂鲁胺是一种经美国食品药品监督管理局批准用于治疗去势抵抗性前列腺癌患者的第二代雄激素受体拮抗剂。不幸的是,接受恩杂鲁胺治疗的患者最终会通过各种复杂机制产生耐药性。本综述探讨了有关这些耐药机制的新信息,包括雄激素受体相关信号通路、糖皮质激素受体相关通路和代谢效应。值得注意的是,还讨论了谱系可塑性和表型转换、基因多态性以及微小RNA与耐药性之间的关系。此外,还提出了针对恩杂鲁胺耐药性去势抵抗性前列腺癌治疗的潜在策略,这有助于发现更有效、更具特异性的治疗方案来克服恩杂鲁胺耐药性。

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