STAT3轴在癌症和癌症干细胞:从肿瘤发生到靶向治疗。

IF 8.3
Deepika Godugu, Rameswari Chilamakuri, Saurabh Agarwal
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引用次数: 0

摘要

转录3的信号转导和激活因子(STAT3)是一种细胞质转录因子,在调节细胞稳态中起重要作用。STAT3的异常和持续激活可触发多种癌症的癌性进展。STAT3可通过规范和非规范途径被激活,导致其核易位并调控多个靶基因的转录,从而促进肿瘤细胞增殖、耐药、分化、炎症、免疫逃避和血管生成。STAT3的持续激活与癌症患者的不良预后相关。值得注意的是,STAT3在癌症干细胞(CSCs)的维持中起着至关重要的作用,导致疾病复发、转移和不良的临床结果。鉴于其在肿瘤生物学中的多方面作用,STAT3是一个有吸引力的治疗干预靶点。目前,各种靶向STAT3的小分子、多肽和天然化合物正处于临床前和临床评估的不同阶段。尽管取得了可喜的进展,但诸如耐药性、选择性和毒性等挑战仍然是开发有效的stat3靶向治疗的障碍。本文综述了STAT3的结构、激活机制及其在肿瘤生物学和CSC维持中的功能作用。我们还强调了STAT3靶向治疗策略的当前进展,包括临床试验中的药物,并讨论了STAT3抑制在精确肿瘤学中的未来潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
STAT3 axis in cancer and cancer stem cells: From oncogenesis to targeted therapies.

The signal transducer and activator of transcription 3 (STAT3) is a cytoplasmic transcription factor that is essential in regulating cellular homeostasis. Aberrant and persistent activation of STAT3 triggers the oncogenic progression of multiple cancers. STAT3 can be activated by both canonical and non-canonical pathways, leading to its nuclear translocation and regulation of the transcription of multiple target genes to promote tumor cell proliferation, drug resistance, differentiation, inflammation, immune evasion, and angiogenesis. Persistent activation of STAT3 correlates with the poor prognosis of cancer patients. Notably, STAT3 plays a crucial role in the maintenance of cancer stem cells (CSCs), contributing to disease relapse, metastasis, and poor clinical outcomes. Given its multifaceted role in tumor biology, STAT3 is an attractive target for therapeutic intervention. Various small molecules, peptides, and natural compounds targeting STAT3 are currently under different stages of preclinical and clinical evaluation. Despite promising advances, challenges such as drug resistance, selectivity, and toxicity remain obstacles in the development of effective STAT3-targeted therapies. This review provides a comprehensive overview of STAT3 structure, activation mechanisms, and its functional role in tumor biology and CSC maintenance. We also highlight current progress in STAT3-targeted therapeutic strategies, including agents in clinical trials, and discuss the future potential of STAT3 inhibition in precision oncology.

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