Integrins as therapeutic targets

被引:366
作者
Goodman, Simon L. [1 ]
Picard, Martin [2 ]
机构
[1] Merck KGaA, Dept Cellular Pharmacol Oncol Platform, D-64271 Darmstadt, Germany
[2] Merck KGaA, Global Clin Dev Unit Oncol, D-64271 Darmstadt, Germany
关键词
ACUTE CORONARY SYNDROMES; MONOCLONAL-ANTIBODY; RECEPTOR ANTAGONIST; BONE TURNOVER; PHASE-II; IN-VIVO; CANCER; CILENGITIDE; INHIBITOR; ALPHA(V)BETA(3);
D O I
10.1016/j.tips.2012.04.002
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Integrins are a large family of molecules that are central regulators in multicellular biology. They orchestrate cell-cell and cell-extracellular matrix (ECM) adhesive interactions from embryonic development to mature tissue function. Diverse human pathologies involve integrin adhesion, including thrombotic diseases, inflammation, cancer, fibrosis and infectious diseases. Integrins are exciting pharmacological targets because they are exposed on the cell surface and are sensitive to pharmacological blockade, but the scale of current efforts involving integrin therapeutics continues to surprise. Several therapeutics targeting integrins are effective drugs: five have been approved for use in clinic, with combined sales of over $1.5 billion in 2010 (based on company reports from that year). We gathered information from three major drug-trial databases and found that similar to 260 anti-integrin drugs have entered clinical trials. Here we overview integrins as drug targets and focus on cancer.
引用
收藏
页码:405 / 412
页数:8
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