Impact of STAT-signaling pathway on cancer-associated fibroblasts in colorectal cancer and its role in immunosuppression

Damián Sánchez-Ramírez, M. G. Mendoza-Rodríguez, Omar R Alemán, Fernando A Candanedo-González, M. Rodríguez-Sosa, J. J. Montesinos-Montesinos, Mauricio Salcedo, Ismael Brito-Toledo, Felipe Vaca-Paniagua, Luis I. Terrazas
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Abstract

Colorectal cancer (CRC) remains one of the most commonly diagnosed and deadliest types of cancer worldwide. CRC displays a desmoplastic reaction (DR) that has been inversely associated with poor prognosis; less DR is associated with a better prognosis. This reaction generates excessive connective tissue, in which cancer-associated fibroblasts (CAFs) are critical cells that form a part of the tumor microenvironment. CAFs are directly involved in tumorigenesis through different mechanisms. However, their role in immunosuppression in CRC is not well understood, and the precise role of signal transducers and activators of transcription (STATs) in mediating CAF activity in CRC remains unclear. Among the myriad chemical and biological factors that affect CAFs, different cytokines mediate their function by activating STAT signaling pathways. Thus, the harmful effects of CAFs in favoring tumor growth and invasion may be modulated using STAT inhibitors. Here, we analyze the impact of different STATs on CAF activity and their immunoregulatory role.
STAT 信号通路对结直肠癌中癌相关成纤维细胞的影响及其在免疫抑制中的作用
结肠直肠癌(CRC)仍然是全球最常见、最致命的癌症类型之一。结直肠癌会出现脱鳞反应(DR),这与预后不良成反比;DR 越少,预后越好。这种反应会产生过多的结缔组织,其中癌症相关成纤维细胞(CAFs)是构成肿瘤微环境一部分的关键细胞。CAFs 通过不同的机制直接参与肿瘤发生。然而,它们在 CRC 免疫抑制中的作用尚不十分清楚,信号转导和转录激活因子(STATs)在介导 CRC 中 CAF 活性方面的确切作用仍不明确。在影响 CAFs 的众多化学和生物因素中,不同的细胞因子通过激活 STAT 信号通路来介导其功能。因此,可以使用 STAT 抑制剂来调节 CAFs 在促进肿瘤生长和侵袭方面的有害作用。在此,我们分析了不同 STAT 对 CAF 活性的影响及其免疫调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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