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Progress in researches about focal adhesion kinase in gastrointestinal tract
Authors:Hui Fang Hao  Yoshio Naomoto  Xiao-Hong Bao  Nobuyuki Watanabe  Kazufumi Sakurama  Kazuhiro Noma  Yasuko Tomono  Takuya Fukazawa  Yasuhiro Shirakawa  Tomoki Yamatsuji  Junji Matsuoka  Munenori Takaoka
Affiliation:Hui Fang Hao, Yoshio Naomoto, Xiao-Hong Bao, Nobuyuki Watanabe, Kazufumi Sakurama, Kazuhiro Noma, Takuya Fukazawa, Yasuhiro Shirakawa, Tomoki Yamatsuji, Junji Matsuoka, Munenori Takaoka, Department of Gastroenterological Surgery, Transplantation and Surgical Oncology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8558, JapanYasuko Tomono, Shigei Medical Research Institute, Okayama 700-8558, Japan
Abstract:Focal adhesion kinase (FAK) is a 125-kDa non-receptor protein tyrosine. Growth factors or the clustering of integrins facilitate the rapid phosphorylation of FAK at Tyr-397 and this in turn recruits Src-family protein tyrosine kinases, resulting in the phosphorylation of Tyr-576 and Tyr-577 in the FAK activation loop and full catalytic FAK activation. FAK plays a critical role in the biological processes of normal and cancer cells including the gastrointestinal tract. FAK also plays an important role in the restitution, cell survival and apoptosis and carcinogenesis of the gastrointestinal tract. FAK is overexpressed in cancer cells and its over-expression and elevated activities are associated with motility and invasion of cancer cells. FAK has been proposed as a potential target in cancer therapy. Small molecule inhibitors effectively inhibit the kinase activity of FAK and show a potent inhibitory effect for the proliferation and migration of tumor cells, indicating a high potential for application in cancer therapy.
Keywords:Focal adhesion kinase  Restitution  Survival and apoptosis  Cancer  Inhibitor
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点击此处可从《World journal of gastroenterology : WJG》浏览原始摘要信息
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