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靶向血管生成用于治疗人类癌症。

Targeting angiogenesis for treatment of human cancer.

作者信息

Somani R R, Bhanushali U V

机构信息

Department of Pharmaceutical Chemistry, VES's College of Pharmacy, Chembur, Mumbai-400 074, India.

出版信息

Indian J Pharm Sci. 2013 Jan;75(1):3-10. doi: 10.4103/0250-474X.113529.

DOI:10.4103/0250-474X.113529
PMID:23901154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3719146/
Abstract

Recent advances in cancer research highlighted the importance of target-specific drug discovery. In view of these advances, the most important mechanism in tumour growth is its ability to stimulate the formation of blood capillaries around itself called tumour-driven angiogenesis. Hence targeting the angiogenesis, inhibits the growth of blood vessels around it and responsible for death of the tumour due to starvation and accumulation of toxic waste. The therapy, thus, indirectly cytotoxic to the tumour cells by targeting newly developing blood vessels. In this review, we summarised the various antiangiogenic agents with their clinical uses and current status.

摘要

癌症研究的最新进展凸显了靶向特异性药物研发的重要性。鉴于这些进展,肿瘤生长中最重要的机制是其刺激自身周围形成毛细血管的能力,即肿瘤驱动的血管生成。因此,针对血管生成进行靶向治疗,可抑制肿瘤周围血管的生长,并导致肿瘤因饥饿和有毒废物积累而死亡。因此,这种疗法通过靶向新生成的血管对肿瘤细胞具有间接的细胞毒性。在本综述中,我们总结了各种抗血管生成药物及其临床应用和现状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/e9941eff5252/IJPhS-75-3-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/9bfff7f363aa/IJPhS-75-3-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/b3a866c7f434/IJPhS-75-3-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/d215c1fc99e6/IJPhS-75-3-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/181d3ea55c2f/IJPhS-75-3-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/7199190c9424/IJPhS-75-3-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/e9941eff5252/IJPhS-75-3-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/9bfff7f363aa/IJPhS-75-3-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/b3a866c7f434/IJPhS-75-3-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/d215c1fc99e6/IJPhS-75-3-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/181d3ea55c2f/IJPhS-75-3-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/7199190c9424/IJPhS-75-3-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/3719146/e9941eff5252/IJPhS-75-3-g010.jpg

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Vandetanib (ZD6474), a dual inhibitor of vascular endothelial growth factor receptor (VEGFR) and epidermal growth factor receptor (EGFR) tyrosine kinases: current status and future directions.凡德他尼(ZD6474),一种血管内皮生长因子受体(VEGFR)和表皮生长因子受体(EGFR)酪氨酸激酶的双重抑制剂:现状与未来方向。
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西妥昔单抗用于治疗结直肠癌。
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Panitumumab, a monoclonal anti epidermal growth factor receptor antibody in colorectal cancer: another one or the one?帕尼单抗,一种用于结直肠癌的单克隆抗表皮生长因子受体抗体:是另一种还是唯一的一种?
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FDA drug approval summary: panitumumab (Vectibix).美国食品药品监督管理局药物批准摘要:帕尼单抗(维克替比)。
Oncologist. 2007 May;12(5):577-83. doi: 10.1634/theoncologist.12-5-577.
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Target practice: lessons from phase III trials with bevacizumab and vatalanib in the treatment of advanced colorectal cancer.靶向治疗实践:贝伐单抗和瓦他拉尼治疗晚期结直肠癌的Ⅲ期试验经验教训
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Development trends for monoclonal antibody cancer therapeutics.单克隆抗体癌症治疗药物的发展趋势。
Nat Rev Drug Discov. 2007 May;6(5):349-56. doi: 10.1038/nrd2241.
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