Borst Rowie, Meyaard Linde, Pascoal Ramos M Ines
Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Oncode Institute, Utrecht, The Netherlands.
J Transl Med. 2024 Apr 24;22(1):382. doi: 10.1186/s12967-024-05199-3.
Tumors are highly complex and heterogenous ecosystems where malignant cells interact with healthy cells and the surrounding extracellular matrix (ECM). Solid tumors contain large ECM deposits that can constitute up to 60% of the tumor mass. This supports the survival and growth of cancerous cells and plays a critical role in the response to immune therapy. There is untapped potential in targeting the ECM and cell-ECM interactions to improve existing immune therapy and explore novel therapeutic strategies. The most abundant proteins in the ECM are the collagen family. There are 28 different collagen subtypes that can undergo several post-translational modifications (PTMs), which alter both their structure and functionality. Here, we review current knowledge on tumor collagen composition and the consequences of collagen PTMs affecting receptor binding, cell migration and tumor stiffness. Furthermore, we discuss how these alterations impact tumor immune responses and how collagen could be targeted to treat cancer.
肿瘤是高度复杂且异质性的生态系统,其中恶性细胞与健康细胞及周围的细胞外基质(ECM)相互作用。实体瘤含有大量的ECM沉积物,其可占肿瘤质量的60%。这支持癌细胞的存活和生长,并在免疫治疗反应中起关键作用。靶向ECM和细胞 - ECM相互作用以改善现有免疫治疗并探索新的治疗策略具有尚未开发的潜力。ECM中最丰富的蛋白质是胶原蛋白家族。有28种不同的胶原蛋白亚型,它们可经历多种翻译后修饰(PTM),这会改变它们的结构和功能。在这里,我们综述了关于肿瘤胶原蛋白组成的现有知识以及影响受体结合、细胞迁移和肿瘤硬度的胶原蛋白PTM的后果。此外,我们讨论了这些改变如何影响肿瘤免疫反应以及如何靶向胶原蛋白来治疗癌症。