靶向雄激素受体信号通路的天然产物:治疗潜力和机制。

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sitong Wu, Esveidy Isabel Oceguera Nava, Dennis Ashong, Guanglin Chen, Qiao-Hong Chen
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引用次数: 0

摘要

雄激素受体(AR)信号通路是前列腺癌发生和发展的主要驱动因素,包括去势抵抗性前列腺癌(CRPC)的发展。由于目前的AR靶向治疗不可避免地会遇到耐药性,因此迫切需要新的策略来抑制AR信号。天然产物代表了丰富且结构多样的生物活性化合物来源,能够在多个调节水平上靶向AR。本文综述了天然产物与AR信号轴之间通过不同机制的相互作用,包括抑制睾酮产生和5α-还原酶活性,直接拮抗AR和诱导AR降解。此外,一些化合物破坏AR核易位,下调AR剪接变异体,或通过表观遗传调节、microRNA调节或干扰共调节网络间接抑制AR信号传导。临床前研究提供了令人信服的证据,表明这些药物可以有效地阻断AR信号,从而抑制前列腺癌的生长。然而,挑战仍然存在,特别是有限的药代动力学表征,缺乏体内验证和缺乏临床研究。未来的研究应侧重于提高生物利用度,探索与现有疗法的协同组合,并推进精心设计的体内和临床研究。总的来说,这些努力可能会建立天然产物作为先导化合物来调节前列腺癌预防和治疗的AR信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Natural Products Targeting the Androgen Receptor Signaling Pathway: Therapeutic Potential and Mechanisms.

Natural Products Targeting the Androgen Receptor Signaling Pathway: Therapeutic Potential and Mechanisms.

Natural Products Targeting the Androgen Receptor Signaling Pathway: Therapeutic Potential and Mechanisms.

Natural Products Targeting the Androgen Receptor Signaling Pathway: Therapeutic Potential and Mechanisms.

The androgen receptor (AR) signaling pathway is the primary driver of prostate cancer initiation and progression, including the development of castration-resistant prostate cancer (CRPC). Because current AR-targeted therapies inevitably encounter drug resistance, novel strategies to suppress AR signaling are urgently needed. Natural products represent a rich and structurally diverse source of bioactive compounds capable of targeting AR at multiple regulatory levels. This review overviews the interactions between natural products and the AR signaling axis through distinct mechanisms, including inhibition of testosterone production and 5α-reductase activity, direct antagonism of AR, and induction of AR degradation. In addition, several compounds disrupt AR nuclear translocation, downregulate AR splice variants, or suppress AR signaling indirectly through epigenetic regulation, microRNA modulation, or interference with co-regulator networks. Preclinical studies provide compelling evidence that these agents can effectively interrupt AR signaling, thereby suppressing prostate cancer growth. However, challenges remain, particularly the limited pharmacokinetic characterization, lack of in vivo validation, and scarcity of clinical studies. Future research should focus on improving bioavailability, exploring synergistic combinations with existing therapies, and advancing well-designed in vivo and clinical investigations. Collectively, these efforts may establish natural products as lead compounds to modulate AR signaling for prostate cancer prevention and treatment.

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来源期刊
Current Issues in Molecular Biology
Current Issues in Molecular Biology 生物-生化研究方法
CiteScore
2.90
自引率
3.20%
发文量
380
审稿时长
>12 weeks
期刊介绍: Current Issues in Molecular Biology (CIMB) is a peer-reviewed journal publishing review articles and minireviews in all areas of molecular biology and microbiology. Submitted articles are subject to an Article Processing Charge (APC) and are open access immediately upon publication. All manuscripts undergo a peer-review process.
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