Samad Md Abdus, Ahmad Iftikhar, Hasan Aakifah, Alhashmi Mohammad Hassan, Ayub Arusha, Al-Abbasi Fahad A, Kumer Ajoy, Tabrez Shams
Department of Biochemistry Faculty of Science King Abdulaziz University Jeddah Saudi Arabia.
King Fahd Medical Research Center King Abdulaziz University Jeddah Saudi Arabia.
MedComm (2020). 2025 Mar 30;6(4):e70152. doi: 10.1002/mco2.70152. eCollection 2025 Apr.
Signal transducer and activator of transcription 3 (STAT3) is a critical transcription factor involved in multiple physiological and pathological processes. While STAT3 plays an essential role in homeostasis, its persistent activation has been implicated in the pathogenesis of various diseases, particularly cancer, bone-related diseases, autoimmune disorders, inflammatory diseases, cardiovascular diseases, and neurodegenerative conditions. The interleukin-6/Janus kinase (JAK)/STAT3 signaling axis is central to STAT3 activation, influencing tumor microenvironment remodeling, angiogenesis, immune evasion, and therapy resistance. Despite extensive research, the precise mechanisms underlying dysregulated STAT3 signaling in disease progression remain incompletely understood, and no United States Food and Drug Administration (USFDA)-approved direct STAT3 inhibitors currently exist. This review provides a comprehensive evaluation of STAT3's role in health and disease, emphasizing its involvement in cancer stem cell maintenance, metastasis, inflammation, and drug resistance. We systematically discuss therapeutic strategies, including JAK inhibitors (tofacitinib, ruxolitinib), Src Homology 2 domain inhibitors (S3I-201, STATTIC), antisense oligonucleotides (AZD9150), and nanomedicine-based drug delivery systems, which enhance specificity and bioavailability while reducing toxicity. By integrating molecular mechanisms, disease pathology, and emerging therapeutic interventions, this review fills a critical knowledge gap in STAT3-targeted therapy. Our insights into STAT3 signaling crosstalk, epigenetic regulation, and resistance mechanisms offer a foundation for developing next-generation STAT3 inhibitors with greater clinical efficacy and translational potential.
信号转导与转录激活因子3(STAT3)是一种关键的转录因子,参与多种生理和病理过程。虽然STAT3在体内平衡中起着至关重要的作用,但其持续激活与多种疾病的发病机制有关,特别是癌症、骨相关疾病、自身免疫性疾病、炎症性疾病、心血管疾病和神经退行性疾病。白细胞介素-6/Janus激酶(JAK)/STAT3信号轴是STAT3激活的核心,影响肿瘤微环境重塑、血管生成、免疫逃逸和治疗耐药性。尽管进行了广泛的研究,但疾病进展中STAT3信号失调的精确机制仍未完全理解,目前尚无美国食品药品监督管理局(USFDA)批准的直接STAT3抑制剂。本综述全面评估了STAT3在健康和疾病中的作用,强调其在癌症干细胞维持、转移、炎症和耐药性中的作用。我们系统地讨论了治疗策略,包括JAK抑制剂(托法替布、鲁索替尼)、Src同源2结构域抑制剂(S3I-201、STATTIC)、反义寡核苷酸(AZD9150)和基于纳米医学的药物递送系统,这些系统在提高特异性和生物利用度的同时降低了毒性。通过整合分子机制、疾病病理学和新兴治疗干预措施,本综述填补了STAT3靶向治疗方面的关键知识空白。我们对STAT3信号串扰、表观遗传调控和耐药机制的见解为开发具有更高临床疗效和转化潜力的下一代STAT3抑制剂奠定了基础。