Roles of c-Met and RON Kinases in tumor progression and their potential as therapeutic targets

被引:52
作者
Chang, Katherine [1 ,2 ]
Karnad, Anand [1 ,2 ]
Zhao, Shujie [1 ]
Freeman, James W. [1 ,2 ,3 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Div Med Oncol, Dept Med, San Antonio, TX 78229 USA
[2] Canc Therapy & Res Ctr S Texas, Expt & Dev Therapeut Program, San Antonio, TX 78229 USA
[3] Audie L Murphy Mem Vet Adm Med Ctr, Res & Dev, San Antonio, TX USA
关键词
c-Met; RON kinase; Met inhibitors; RECEPTOR TYROSINE KINASE; HEPATOCYTE GROWTH-FACTOR; CELL LUNG-CANCER; PANCREATIC-CANCER; STEM-CELLS; TUMORIGENIC ACTIVITIES; SIGNALING PATHWAY; POINT MUTATIONS; POOR-PROGNOSIS; COLON-CANCER;
D O I
10.18632/oncotarget.3420
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
c-Met and receptor originated from nantes (RON) are structurally related transmembrane phosphotyrosine kinase receptors. c-Met and RON show increased expression or activity in a variety of tumors leading to tumor progression and may play a role in acquired resistance to therapy. Although often co-expressed, the distinct functional roles of c-Met and RON are not fully understood. c-Met and RON form both activated homodimers and heterodimers with themselves and other families of phosphotyrosine kinase receptors. Inhibitors for c-Met and RON including small molecular weigh kinase inhibitors and neutralizing antibodies are in pre-clinical investigation and clinical trials. Several of the tyrosine kinase inhibitors have activity against both c-Met and RON kinases whereas the antibodies generally are target specific. As with many targeted agents used to treat solid tumors, it is likely that c-Met/RON inhibitors will have greater benefit when used in combination with chemotherapy or other targeted agents. A careful analysis of c-Met/RON expression or activity and a better elucidation of how they influence cell signaling will be useful in predicting which tumors respond best to these inhibitors as well as determining which agents can be used with these inhibitors for combined therapy.
引用
收藏
页码:3507 / 3518
页数:12
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