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通过靶向 CLEC14a 的优化抗体抑制 VEGF 依赖性血管生成和肿瘤血管生成。

Inhibition of VEGF-dependent angiogenesis and tumor angiogenesis by an optimized antibody targeting CLEC14a.

机构信息

Scripps Korea Antibody Institute, Chuncheon, South Korea.

Research Institute, National Cancer Center, Goyang, South Korea.

出版信息

Mol Oncol. 2018 Mar;12(3):356-372. doi: 10.1002/1878-0261.12169. Epub 2018 Jan 26.

DOI:10.1002/1878-0261.12169
PMID:29316206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5830631/
Abstract

The C-type lectin-like domain of CLEC14a (CLEC14a-C-type lectin-like domain [CTLD]) is a key domain that mediates endothelial cell-cell contacts in angiogenesis. However, the role of CLEC14a-CTLD in pathological angiogenesis has not yet been clearly elucidated. In this study, through complementarity-determining region grafting, consecutive deglycosylation, and functional isolation, we generated a novel anti-angiogenic human monoclonal antibody that specifically targets CLEC14a-CTLD and that shows improved stability and homogeneity relative to the parental antibody. We found that this antibody directly inhibits CLEC14a-CTLD-mediated endothelial cell-cell contact and simultaneously downregulates expression of CLEC14a on the surface of endothelial cells. Using various in vitro and in vivo functional assays, we demonstrated that this antibody effectively suppresses vascular endothelial growth factor (VEGF)-dependent angiogenesis and tumor angiogenesis of SNU182 human hepatocellular carcinoma, CFPAC-1 human pancreatic cancer, and U87 human glioma cells. Furthermore, we also found that this antibody significantly inhibits tumor angiogenesis of HCT116 and bevacizumab-adapted HCT116 human colorectal cancer cells. These findings suggest that antibody targeting of CLEC14a-CTLD has the potential to suppress VEGF-dependent angiogenesis and tumor angiogenesis and that CLEC14a-CTLD may be a novel anti-angiogenic target for VEGF-dependent angiogenesis and tumor angiogenesis.

摘要

CLEC14a 的 C 型凝集素样结构域(CLEC14a-C 型凝集素样结构域 [CTLD])是介导血管生成中内皮细胞-细胞接触的关键结构域。然而,CLEC14a-CTLD 在病理性血管生成中的作用尚未得到明确阐明。在这项研究中,通过互补决定区移植、连续去糖基化和功能分离,我们产生了一种新型抗血管生成的人源单克隆抗体,该抗体特异性靶向 CLEC14a-CTLD,与亲本抗体相比具有更好的稳定性和均一性。我们发现该抗体可直接抑制 CLEC14a-CTLD 介导的内皮细胞-细胞接触,并同时下调内皮细胞表面 CLEC14a 的表达。通过各种体外和体内功能测定,我们证明该抗体可有效抑制血管内皮生长因子 (VEGF) 依赖性血管生成和 SNU182 人肝癌、CFPAC-1 人胰腺癌细胞和 U87 人神经胶质瘤细胞的肿瘤血管生成。此外,我们还发现该抗体可显著抑制 HCT116 和贝伐单抗适应的 HCT116 人结直肠癌细胞的肿瘤血管生成。这些发现表明,针对 CLEC14a-CTLD 的抗体具有抑制 VEGF 依赖性血管生成和肿瘤血管生成的潜力,并且 CLEC14a-CTLD 可能是 VEGF 依赖性血管生成和肿瘤血管生成的新型抗血管生成靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13e4/5830631/7124e57cd799/MOL2-12-356-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13e4/5830631/6f7b9e0a3cb0/MOL2-12-356-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13e4/5830631/d3126a202f94/MOL2-12-356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13e4/5830631/123529fffab8/MOL2-12-356-g003.jpg
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