Tumor Blood Vessels and Vasculogenic Mimicry – Current Knowledge and Searching for New Cellular/Molecular Targets of Anti-Angiogenic Therapy

A. Knopik-Skrocka, P. Kreplewska, D. Jarmołowska-Jurczyszyn
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引用次数: 9

Abstract

Summary Blood vessel formation in tumor is defined as tumor angiogenesis. So far, the most known its mechanism is sprouting, which means formation of blood vessels from existing ones, as a result of the proliferation and migration of endothelial cells. The main mitogenic factor of these cells is vascular endothelial growth factor VEGF, acting by VEGFR-2 receptors. Recent studies have provided knowledge about the ability of tumors to form vessel-like structures. The phenomenon was called vascular mimicry. Tumor cells show a high plasticity and they can undergo differentiation to the ones with phenotype similar to endothelial cells. Each of the known tumor angiogenesis mechanisms is a result of many different factors and cell cooperation in tumor microenvironment. Tumor ability to the heterogeneous vascularization forces developing of complex, anti-angiogenic therapy directed to different molecular and cellular targets. Therapies, used so far, often lead to drug-induced hypoxia, which increases tumor cell aggressiveness and metastasis.
肿瘤血管和血管生成模拟-目前的知识和寻找新的抗血管生成治疗的细胞/分子靶点
肿瘤血管形成被定义为肿瘤血管生成。到目前为止,最广为人知的机制是发芽,即内皮细胞增殖和迁移的结果,由现有的血管形成血管。这些细胞的主要有丝分裂因子是血管内皮生长因子VEGF,通过VEGFR-2受体起作用。最近的研究提供了关于肿瘤形成血管样结构的能力的知识。这种现象被称为血管模仿。肿瘤细胞具有较高的可塑性,可分化为与内皮细胞表型相似的细胞。每一种已知的肿瘤血管生成机制都是肿瘤微环境中多种不同因素和细胞协同作用的结果。肿瘤对异质血管生成力的能力发展复杂,针对不同分子和细胞靶点的抗血管生成治疗。目前使用的治疗方法通常会导致药物性缺氧,从而增加肿瘤细胞的侵袭性和转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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