Kuriyama Naoya, Yoshioka Yusuke, Kikuchi Shinsuke, Azuma Nobuyoshi, Ochiya Takahiro
Division of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, Tokyo, Japan.
Department of Vascular Surgery, Asahikawa Medical University, Asahikawa, Japan.
Front Cell Dev Biol. 2020 Dec 9;8:611039. doi: 10.3389/fcell.2020.611039. eCollection 2020.
Tumor progression involves a series of biologically important steps in which the crosstalk between cancer cells and the surrounding environment is an important issue. Angiogenesis is a key tumorigenic phenomenon for cancer progression. Tumor-related extracellular vesicles (EVs) modulate the tumor microenvironment (TME) through cell-to-cell communication. Tumor cells in a hypoxic TME release more EVs than cells in a normoxic environment due to uncontrollable tumor proliferation. Tumor-derived EVs in the TME influence endothelial cells (ECs), which then play multiple roles, contributing to tumor angiogenesis, loss of the endothelial vascular barrier by binding to ECs, and subsequent endothelial-to-mesenchymal transition. In contrast, they also indirectly induce tumor angiogenesis through the phenotype switching of various cells into cancer-associated fibroblasts, the activation of tumor-associated ECs and platelets, and remodeling of the extracellular matrix. Here, we review current knowledge regarding the involvement of EVs in tumor vascular-related cancer progression.
肿瘤进展涉及一系列生物学上重要的步骤,其中癌细胞与周围环境之间的相互作用是一个重要问题。血管生成是癌症进展的关键致瘤现象。肿瘤相关的细胞外囊泡(EVs)通过细胞间通讯调节肿瘤微环境(TME)。由于肿瘤增殖失控,处于缺氧TME中的肿瘤细胞比处于常氧环境中的细胞释放更多的EVs。TME中肿瘤来源的EVs影响内皮细胞(ECs),内皮细胞随后发挥多种作用,促进肿瘤血管生成、通过与ECs结合导致内皮血管屏障丧失以及随后的内皮-间充质转化。相反,它们还通过将各种细胞的表型转变为癌症相关成纤维细胞、激活肿瘤相关ECs和血小板以及细胞外基质重塑间接诱导肿瘤血管生成。在此,我们综述了关于EVs参与肿瘤血管相关癌症进展的当前知识。