Kay Emily J, Koulouras Grigorios, Zanivan Sara
Cancer Research UK Beatson Institute, Glasgow, United Kingdom.
Institute of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.
Front Oncol. 2021 Aug 27;11:719922. doi: 10.3389/fonc.2021.719922. eCollection 2021.
Cancer associated fibroblasts (CAFs) are a major component of the tumour microenvironment in most tumours, and are key mediators of the response to tissue damage caused by tumour growth and invasion, contributing to the observation that tumours behave as 'wounds that do not heal'. CAFs have been shown to play a supporting role in all stages of tumour progression, and this is dependent on the highly secretory phenotype CAFs develop upon activation, of which extracellular matrix (ECM) production is a key element. A collagen rich, stromal ECM has been shown to influence tumour growth and metastasis, exclude immune cells and impede drug delivery, and is associated with poor prognosis in many cancers. CAFs also extensively remodel their metabolism to support cancer cells, however, it is becoming clear that metabolic rewiring also supports intrinsic functions of activated fibroblasts, such as increased ECM production. In this review, we summarise how fibroblasts metabolically regulate ECM production, focussing on collagen production, at the transcriptional, translational and post-translational level, and discuss how this can provide possible strategies for effectively targeting CAF activation and formation of a tumour-promoting stroma.
癌症相关成纤维细胞(CAFs)是大多数肿瘤中肿瘤微环境的主要组成部分,是对肿瘤生长和侵袭所导致的组织损伤作出反应的关键介质,这也解释了肿瘤为何表现为“无法愈合的伤口”。研究表明,CAFs在肿瘤进展的各个阶段均发挥支持作用,这取决于CAFs激活后所呈现的高分泌表型,其中细胞外基质(ECM)的产生是关键要素。富含胶原蛋白的基质ECM已被证明会影响肿瘤生长和转移、排斥免疫细胞并阻碍药物递送,且与多种癌症的不良预后相关。CAFs还会广泛重塑其代谢以支持癌细胞,然而,越来越清楚的是,代谢重编程也支持活化成纤维细胞的固有功能,例如增加ECM的产生。在本综述中,我们总结了成纤维细胞如何在转录、翻译和翻译后水平上代谢调节ECM的产生,重点是胶原蛋白的产生,并讨论这如何为有效靶向CAF激活和促进肿瘤的基质形成提供可能的策略。