IFOM - The FIRC Institute of Molecular Oncology, Milan, Italy.
Semin Cancer Biol. 2009 Oct;19(5):298-309. doi: 10.1016/j.semcancer.2009.05.004. Epub 2009 May 29.
Cell adhesion molecules (CAMs) are cell surface glycoproteins that mediate the physical interactions between adjacent cells and between cells and the surrounding extracellular matrix. CAMs belong to different protein families, depending on their structural and functional properties. Furthermore, the expression of certain CAMs under physiological conditions is restricted to specific cell types. Besides playing a key homeostatic role in maintaining the architecture of quiescent tissues, CAMs have also to adapt to the microenvironmental changes that occur during certain physiological and pathological processes. This is best exemplified by cancer vascularization, where the expression and function of vascular CAMs are dynamically regulated in response to tissue alterations induced by tumor growth as well as by changes in the surrounding stroma. This enables endothelial cells (ECs) to leave the quiescent state and re-enter the angiogenic cascade. The latter is a multistep process carried out by different types of specialized ECs. This review describes the actual or supposed function of the various CAM subsets in the sequential series of events that underlie vascular changes during tumor angiogenesis. Notably, elucidating the mechanism of action of endothelial CAMs in cancer vasculature is expected to open new therapeutic avenues aimed at interfering with tumor growth and dissemination.
细胞黏附分子 (CAMs) 是细胞表面糖蛋白,介导相邻细胞之间以及细胞与周围细胞外基质之间的物理相互作用。CAMs 根据其结构和功能特性属于不同的蛋白质家族。此外,某些 CAMs 在生理条件下的表达仅限于特定的细胞类型。CAMs 在维持静止组织的结构方面发挥着关键的稳态作用,除了这一点,CAMs 还需要适应某些生理和病理过程中发生的微环境变化。肿瘤血管生成就是最好的例证,其中血管 CAMs 的表达和功能会根据肿瘤生长引起的组织改变以及周围基质的变化而动态调节。这使得内皮细胞 (ECs) 能够离开静止状态并重新进入血管生成级联反应。后者是由不同类型的专门 ECs 进行的多步过程。本文综述了各种 CAM 亚群在肿瘤血管生成过程中血管变化的一系列连续事件中的实际或推测功能。值得注意的是,阐明内皮细胞 CAMs 在癌症血管中的作用机制有望开辟新的治疗途径,旨在干扰肿瘤生长和扩散。