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CXCL12 (SDF1alpha)-CXCR4/CXCR7 pathway inhibition: an emerging sensitizer for anticancer therapies?CXCL12(SDF1alpha)-CXCR4/CXCR7 通路抑制:一种新兴的抗肿瘤治疗增敏剂?
Clin Cancer Res. 2011 Apr 15;17(8):2074-80. doi: 10.1158/1078-0432.CCR-10-2636. Epub 2011 Feb 24.
2
HRG inhibits tumor growth and metastasis by inducing macrophage polarization and vessel normalization through downregulation of PlGF.HRG 通过下调 PlGF 诱导巨噬细胞极化和血管正常化来抑制肿瘤生长和转移。
Cancer Cell. 2011 Jan 18;19(1):31-44. doi: 10.1016/j.ccr.2010.11.009. Epub 2011 Jan 6.
3
Glioblastoma recurrence after cediranib therapy in patients: lack of "rebound" revascularization as mode of escape.西地尼布治疗后胶质母细胞瘤复发的患者:无“反弹”血管生成作为逃逸模式。
Cancer Res. 2011 Jan 1;71(1):19-28. doi: 10.1158/0008-5472.CAN-10-2602.
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7
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Pericytes: blood-brain barrier safeguards against neurodegeneration?周细胞:血脑屏障对神经退行性变的保护作用?
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血管生成的分子机制与临床应用。

Molecular mechanisms and clinical applications of angiogenesis.

机构信息

Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, VIB, Leuven B-3000, Belgium.

出版信息

Nature. 2011 May 19;473(7347):298-307. doi: 10.1038/nature10144.

DOI:10.1038/nature10144
PMID:21593862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4049445/
Abstract

Blood vessels deliver oxygen and nutrients to every part of the body, but also nourish diseases such as cancer. Over the past decade, our understanding of the molecular mechanisms of angiogenesis (blood vessel growth) has increased at an explosive rate and has led to the approval of anti-angiogenic drugs for cancer and eye diseases. So far, hundreds of thousands of patients have benefited from blockers of the angiogenic protein vascular endothelial growth factor, but limited efficacy and resistance remain outstanding problems. Recent preclinical and clinical studies have shown new molecular targets and principles, which may provide avenues for improving the therapeutic benefit from anti-angiogenic strategies.

摘要

血管将氧气和营养物质输送到身体的各个部位,但也滋养着癌症等疾病。在过去的十年中,我们对血管生成(血管生长)分子机制的理解呈爆炸式增长,并已批准将抗血管生成药物用于癌症和眼部疾病。到目前为止,已有数十万患者受益于血管内皮生长因子等血管生成蛋白的抑制剂,但疗效有限和耐药性仍是突出问题。最近的临床前和临床研究表明了新的分子靶点和原理,这可能为提高抗血管生成策略的治疗效果提供途径。