Reeva Hazel, Mahesh Godson, Manjunath Uma, Selvamurugan Nagarajan, MohanKumar Durairaj
Department of Biotechnology, School of Bioengineering, SRM Institute of science and Technology, Kattankulathur, Tamil Nadu, 603 203.
Department of Biotechnology, School of Bioengineering, SRM Institute of science and Technology, Kattankulathur, Tamil Nadu, 603 203.
Semin Oncol. 2025 Jun;52(3):152346. doi: 10.1016/j.seminoncol.2025.152346. Epub 2025 May 29.
The complex interplay between collagen and cancer cells within the tumor microenvironment (TME) highlights the pivotal role of collagens in cancer progression, prognosis and therapy resistance. As a critical structural protein of the extracellular matrix (ECM), collagen not only maintains tissue architecture but also regulates key physiological functions through complex biosynthetic pathways. Deregulation in collagen biosynthesis, characterized by abnormal transcription, post-translational modifications, and deposition, contributes to ECM remodeling and tumor progression. This review explores the involvement of diverse collagen family members in cancer progression across multiple cancer types. Several collagen isoforms have emerged as key players in cancer progression, influencing tumor behavior and act as potential biomarkers for prognosis. Furthermore, circulating collagen fragments in blood present promising avenues for non-invasive cancer diagnosis and disease monitoring. Tumor collagen remodeling alters ECM architecture, impacting tumor-stromal interactions and fostering a microenvironment conducive to favour invasion and metastasis. Mechanistic insights reveal that collagen-induced signalling pathways are the major drivers of stemness, drug resistance, EMT, metastasis, angiogenesis and immune evasion, which collectively shape tumor cell behavior and immune infiltration dynamics. Further, targeting tumor collagen appear to be a viable and robust strategy to treat aggressive desmoplastic and metastatic cancers.
肿瘤微环境(TME)中胶原蛋白与癌细胞之间复杂的相互作用凸显了胶原蛋白在癌症进展、预后及治疗耐药性方面的关键作用。作为细胞外基质(ECM)的一种关键结构蛋白,胶原蛋白不仅维持组织结构,还通过复杂的生物合成途径调节关键生理功能。胶原蛋白生物合成失调,其特征为转录异常、翻译后修饰及沉积异常,会导致ECM重塑和肿瘤进展。本综述探讨了多种胶原蛋白家族成员在多种癌症类型的癌症进展中的参与情况。几种胶原蛋白亚型已成为癌症进展的关键因素,影响肿瘤行为,并可作为预后的潜在生物标志物。此外,血液中循环的胶原蛋白片段为非侵入性癌症诊断和疾病监测提供了有前景的途径。肿瘤胶原蛋白重塑改变了ECM结构,影响肿瘤-基质相互作用,并营造了有利于侵袭和转移的微环境。机制研究表明,胶原蛋白诱导的信号通路是干性、耐药性、上皮-间质转化(EMT)、转移、血管生成和免疫逃逸的主要驱动因素,这些因素共同塑造了肿瘤细胞行为和免疫浸润动态。此外,靶向肿瘤胶原蛋白似乎是治疗侵袭性促纤维增生性和转移性癌症的一种可行且有力的策略。