Focal Adhesion Kinase as a Cancer Therapy Target

被引:3
作者
Golubovskaya, Vita M. [1 ,2 ]
机构
[1] Roswell Pk Canc Inst, Dept Surg Oncol, Buffalo, NY 14263 USA
[2] SUNY Buffalo, Buffalo, NY 14260 USA
关键词
Adhesion; cancer; Focal Adhesion Kinase; inhibitor; metastasis; tumor; SQUAMOUS-CELL CARCINOMA; DECREASES TUMOR-GROWTH; PANCREATIC ADENOCARCINOMA CELLS; SMALL-MOLECULE INHIBITOR; TIME PCR ANALYSES; HUMAN NEUROBLASTOMA; UP-REGULATION; COLON-CANCER; LUNG-CANCER; TYROSINE PHOSPHORYLATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that resides at the sites of at focal adhesions. The 125 kDa FAK protein is encoded by the FAK gene located on human chromosome 8q24. Structurally, FAK consists of an amino-terminal regulatory FERM domain, a central catalytic kinase domain, and a carboxy-terminal focal adhesion targeting domain. FAK has been shown to be an important mediator of cell adhesion, growth, proliferation, survival, angiogenesis and migration, all of which are often disrupted in cancer cells. Normal tissues have low expression of FAK, while primary and metastatic tumors significantly overexpress this protein. This review summarizes expression of FAK by immunohistochemical staining in different tumor types and presents several FAK inhibition therapy approaches.
引用
收藏
页码:735 / 741
页数:7
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