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重组CD44-HABD是一种新型强效直接血管生成抑制剂,可独立于透明质酸结合而增强内皮细胞特异性生长抑制作用。

Recombinant CD44-HABD is a novel and potent direct angiogenesis inhibitor enforcing endothelial cell-specific growth inhibition independently of hyaluronic acid binding.

作者信息

Päll Taavi, Gad Annica, Kasak Lagle, Drews Monika, Strömblad Staffan, Kogerman Priit

机构信息

Department of Laboratory Medicine, Karolinska Institutet, Huddinge University Hospital F 46, Huddinge, 141 86 Huddinge, Sweden.

出版信息

Oncogene. 2004 Oct 14;23(47):7874-81. doi: 10.1038/sj.onc.1208083.

Abstract

CD44 is the main cellular receptor for hyaluronic acid (HA). We previously found that overexpression of CD44 inhibited tumor growth of mouse fibrosarcoma cells in mice. Here, we show that soluble recombinant CD44 HA-binding domain (CD44-HABD) acts directly onto endothelial cells by inhibiting endothelial cell proliferation in a cell-specific manner. Consequently, soluble recombinant CD44-HABD also blocked angiogenesis in vivo in chick and mouse, and thereby inhibited tumor growth of various origins at very low doses (0.25 mg/kg x day). The antiangiogenic effect of CD44 is independent of its HA-binding capacity, since mutants deficient in HA binding still maintain their antiangiogenic and antiproliferative properties. Recombinant CD44-HABD represents a novel class of angiogenesis inhibitors based on a cell-surface receptor.

摘要

CD44是透明质酸(HA)的主要细胞受体。我们之前发现,CD44的过表达抑制了小鼠体内小鼠纤维肉瘤细胞的肿瘤生长。在此,我们表明可溶性重组CD44透明质酸结合结构域(CD44-HABD)通过以细胞特异性方式抑制内皮细胞增殖而直接作用于内皮细胞。因此,可溶性重组CD44-HABD在鸡和小鼠体内也阻断了血管生成,从而以非常低的剂量(0.25毫克/千克×天)抑制了各种来源的肿瘤生长。CD44的抗血管生成作用与其HA结合能力无关,因为缺乏HA结合的突变体仍保持其抗血管生成和抗增殖特性。重组CD44-HABD代表了一类基于细胞表面受体的新型血管生成抑制剂。

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