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An alternatively spliced form of Met receptor is tumorigenic.

Authors
Lee, JH; Gao, CF; Lee, CC; Kim, MD; Vande Woude, GF
Citation
Experimental & molecular medicine, 38(5):565-573, 2006
Journal Title
Experimental & molecular medicine
ISSN
1226-36132092-6413
Abstract
The Met tyrosine kinase receptor is a widely expressed molecule, which mediates pleiotropic cellular responses following activation by its ligand, hepatocyte growth factor/scatter factor (HGF/SF). Previously, one of the authors identified an alternatively spliced form of Met (Met-SM) that lacked a single exon of a 47-amino-acid segment in the juxtamembrane domain. Here we report that Met-SM is a potent transforming gene in NIH3T3 mouse fibroblast cells. Met-SM-transfected NIH3T3 cells show stronger foci-forming activity than wild type- Met-transfected ones. In addition, Met-SM-transfected NIH3T3 cells form colonies in soft agar and are tumorigenic in athymic nu/nu mice. Furthermore, HGF/SF significantly increases the focus-forming activity of Met-SM comparing to wild type Met. The amount of protein and of tyrosine kinase activity of Met-SM accumulates to a high level following HGF/SF treatment. The accumulation of Met-SM correlated well with its delayed ubiquitination and increased stability. These results are consistent with the important role of the juxtamembrane domain in protein stability of Met receptor and suggest that the alternatively-spliced form may contribute to the development and progression of human cancer.
MeSH terms
Alternative Splicing*AnimalsCarcinogenicity TestsCarcinogens/metabolism*Down-RegulationFemaleHepatocyte Growth Factor/pharmacologyMiceMice, NudeMutant Proteins/metabolismMutant Proteins/physiologyNIH 3T3 CellsProtein Isoforms/metabolismProtein Isoforms/physiologyProto-Oncogene Proteins c-met/metabolism*Proto-Oncogene Proteins c-met/physiology*
DOI
10.1038/emm.2006.66
PMID
17079873
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Journal Papers > School of Medicine / Graduate School of Medicine > Biochemistry & Molecular Biology
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