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胶原合成的代谢控制。

Metabolic control of collagen synthesis.

机构信息

Section of Hematology/Oncology, Department of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, 60637, USA.

Section of Hematology/Oncology, Department of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, 60637, USA; Committee on Cancer Biology, Committee on Molecular Metabolism and Nutrition, The University of Chicago, Chicago, IL, 60637, USA.

出版信息

Matrix Biol. 2024 Nov;133:43-56. doi: 10.1016/j.matbio.2024.07.003. Epub 2024 Jul 29.

Abstract

The extracellular matrix (ECM) is present in all tissues and crucial in maintaining normal tissue homeostasis and function. Defects in ECM synthesis and remodeling can lead to various diseases, while overproduction of ECM components can cause severe conditions like organ fibrosis and influence cancer progression and therapy resistance. Collagens are the most abundant core ECM proteins in physiological and pathological conditions and are predominantly synthesized by fibroblasts. Previous efforts to target aberrant collagen synthesis in fibroblasts by inhibiting pro-fibrotic signaling cascades have been ineffective. More recently, metabolic rewiring downstream of pro-fibrotic signaling has emerged as a critical regulator of collagen synthesis in fibroblasts. Here, we propose that targeting the metabolic pathways involved in ECM biomass generation provides a novel avenue for treating conditions characterized by excessive collagen accumulation. This review summarizes the unique metabolic challenges collagen synthesis imposes on fibroblasts and discusses how underlying metabolic networks could be exploited to create therapeutic opportunities in cancer and fibrotic disease. Finally, we provide a perspective on open questions in the field and how conceptual and technical advances will help address them to unlock novel metabolic vulnerabilities of collagen synthesis in fibroblasts and beyond.

摘要

细胞外基质(ECM)存在于所有组织中,对于维持正常组织内稳态和功能至关重要。ECM 合成和重塑的缺陷可导致各种疾病,而 ECM 成分的过度产生可引起严重情况,如器官纤维化,并影响癌症进展和治疗耐药性。在生理和病理条件下,胶原蛋白是最丰富的核心 ECM 蛋白,主要由成纤维细胞合成。先前通过抑制致纤维化信号级联来靶向成纤维细胞中异常胶原合成的努力效果不佳。最近,致纤维化信号下游的代谢重编程已成为成纤维细胞中胶原合成的关键调节因子。在这里,我们提出靶向 ECM 生物量生成所涉及的代谢途径为治疗以胶原过度积累为特征的疾病提供了新的途径。本综述总结了胶原蛋白合成给成纤维细胞带来的独特代谢挑战,并讨论了如何利用潜在的代谢网络在癌症和纤维化疾病中创造治疗机会。最后,我们提供了对该领域开放性问题的看法,以及概念和技术的进步如何帮助解决这些问题,以揭示成纤维细胞中胶原蛋白合成的新代谢脆弱性。

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