Modulation of tumor-induced angiogenesis by proteins of extracellular matrix.

Molecular biotherapy Pub Date : 1991-03-01
A M Eiján, L Davel, S Oisgold-Dagá, E S de Lustig
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Abstract

The formation of new vessels is a known event in enlarging tumors. Furthermore, the metastatic potential is abrogated or reduced markedly in the absence of neovascularization. Shedding of tumor cells into the circulation is not observed until vascularization has occurred. As a result, the interruption of neovascularization could be a good target for cancer control. This research was an attempt to see if two proteins present in extracellular matrix, collagen and fibronectin (FN), could modify the tumor-induced angiogenesis. The strong angiogenic response induced by S13 tumor cells in the skin of BALB/c mice was blocked by treatment with FN and FN-derived peptides. In contrast, collagen did not modify tumor-induced angiogenesis.

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细胞外基质蛋白对肿瘤诱导血管生成的调节作用。
新血管的形成是肿瘤扩大的一个已知事件。此外,在没有新血管形成的情况下,转移潜力被消除或显着降低。直到血管化发生后才观察到肿瘤细胞进入循环。因此,新生血管的中断可能是癌症控制的一个很好的靶点。本研究旨在观察存在于细胞外基质中的胶原蛋白和纤维连接蛋白(FN)是否能改变肿瘤诱导的血管生成。FN和FN衍生肽可阻断BALB/c小鼠皮肤中S13肿瘤细胞诱导的强血管生成反应。相反,胶原蛋白不能改变肿瘤诱导的血管生成。
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