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非前列腺恶性肿瘤中的雄激素受体信号传导:挑战与机遇

Androgen receptor signalling in non-prostatic malignancies: challenges and opportunities.

作者信息

Dotto G Paolo, Buckinx An, Özdemir Berna C, Simon Christian

机构信息

Cutaneous Biology Research Center, Department of Dermatology, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA.

Service d'Oto-rhino-laryngologie et chirurgie cervical faciale, Centre Hospitalier Universitaire Vaudois (CHUV), Université de Lausanne (UNIL), Lausanne, Switzerland.

出版信息

Nat Rev Cancer. 2025 Feb;25(2):93-108. doi: 10.1038/s41568-024-00772-w. Epub 2024 Nov 25.

Abstract

The androgen receptor (AR) signalling pathway has been intensively studied in the context of prostate cancer, where androgen deprivation therapy is part of the standard of care for metastatic disease. By contrast, fewer studies have investigated the impact and translational potential of targeting AR in other cancer types where it is also expressed and functional. In this Review, we discuss the current understanding of AR in non-prostatic cancer types and summarize ongoing AR-directed clinical trials. While different androgen levels contribute to sexual dimorphism in cancer, targeting the AR system could benefit both sexes and help overcome resistance to targeted therapies. However, a bimodal function of AR signalling, which suppresses stromal changes associated with the early stages of cancer development, also needs to be considered. Future research is necessary to scrutinize cellular and molecular mechanisms of action of AR in cancer cells and the tumour microenvironment, to develop selective modulators of AR activity, and to identify patients with non-prostatic cancer who might benefit from targeting this pathway. AR-directed manipulation of host immune cells may offer a promising therapeutic approach for many types of cancers.

摘要

雄激素受体(AR)信号通路在前列腺癌的背景下已得到深入研究,在前列腺癌中,雄激素剥夺疗法是转移性疾病标准治疗的一部分。相比之下,针对在其他也表达且具有功能的癌症类型中靶向AR的影响和转化潜力的研究较少。在本综述中,我们讨论了目前对非前列腺癌类型中AR的理解,并总结了正在进行的针对AR的临床试验。虽然不同的雄激素水平导致癌症中的性别二态性,但靶向AR系统可能对两性都有益,并有助于克服对靶向治疗的耐药性。然而,还需要考虑AR信号传导的双峰功能,它会抑制与癌症发展早期阶段相关的基质变化。未来有必要开展研究,仔细审查AR在癌细胞和肿瘤微环境中的细胞和分子作用机制,开发AR活性的选择性调节剂,并识别可能从靶向该通路中获益的非前列腺癌患者。对宿主免疫细胞进行AR导向的操控可能为多种癌症提供一种有前景的治疗方法。

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