Ahmed Abdulrahman T, Oghenemaro Enwa Felix, Hjazi Ahmed, Jain Vicky, Ahmad Irfan, Roopashree R, Soothwal Pradeep, Goswami Manish, Zwamel Ahmed Hussein, Kdhim Karam
College of Nursing, University of Al Maarif, Al Anbar, 31001, Iraq.
Delta State University, Department of Pharmaceutical Microbiology, Faculty of Pharmacy, PMB 1, Abraka, Delta State, Nigeria.
Cell Biochem Biophys. 2025 Jul 8. doi: 10.1007/s12013-025-01816-0.
The transcriptional regulator signal transducer and activator of transcription 3 (STAT3) plays pivotal roles in vertebrate development and the functionality of mature tissues, particularly in modulating inflammation and immune responses. Mutations in STAT3 in humans are associated with various diseases, including immunodeficiencies, autoimmune disorders, and multiple cancers. Notably, both aberrant hyperactivation and inactivation of STAT3 are linked to disease manifestations, underscoring the need for tightly regulated STAT3 activity to maintain health. In inflammatory bowel disease (IBD), STAT3 exhibits abnormal activation in colonic tissues, primarily driven by a range of pro-inflammatory cytokines. This dysregulation compromises the integrity of the intestinal mucosal barrier and leads to an exaggerated innate immune response and heightened Th17 cell activity. Moreover, persistent STAT3 activation is implicated in the pathogenesis of colorectal cancer (CRC), highlighting its critical regulatory role in inflammation associated with cancer-induced colitis. Elevated STAT3 expression is frequently observed in CRC cases. This study delves into STAT3's multifaceted roles in various cellular processes, including proliferation, migration, differentiation, motility, and the inflammatory response, specifically focusing on their implications in colitis and colorectal cancer. We further explore therapeutic strategies to modulate STAT3 signaling pathways, which could provide innovative approaches for managing STAT3-dependent colonic disorders.
转录调节因子信号转导及转录激活因子3(STAT3)在脊椎动物发育和成熟组织的功能中发挥着关键作用,尤其是在调节炎症和免疫反应方面。人类STAT3基因的突变与多种疾病相关,包括免疫缺陷、自身免疫性疾病和多种癌症。值得注意的是,STAT3的异常过度激活和失活均与疾病表现有关,这凸显了严格调控STAT3活性以维持健康的必要性。在炎症性肠病(IBD)中,STAT3在结肠组织中表现出异常激活,主要由一系列促炎细胞因子驱动。这种失调损害了肠道黏膜屏障的完整性,导致先天性免疫反应过度和Th17细胞活性增强。此外,STAT3的持续激活与结直肠癌(CRC)的发病机制有关,突出了其在与癌症诱导的结肠炎相关的炎症中的关键调节作用。在CRC病例中经常观察到STAT3表达升高。本研究深入探讨了STAT3在各种细胞过程中的多方面作用,包括增殖、迁移、分化、运动和炎症反应,特别关注其在结肠炎和结直肠癌中的意义。我们进一步探索调节STAT3信号通路的治疗策略,这可能为管理依赖STAT3的结肠疾病提供创新方法。