| Literature DB >> 23401136 |
John I Risinger1, Mary Custer, Lionel Feigenbaum, R Mark Simpson, Shelley B Hoover, Joshua D Webster, Gadisetti V R Chandramouli, Lino Tessarollo, J Carl Barrett.
Abstract
The KAI1/CD82 tetraspanin is a widely expressed cell surface molecule thought to organize diverse cellular signaling processes. KAI1/CD82 suppresses metastasis but not tumorigenicity, establishing it as one of a class of metastasis suppressor genes. In order to further assess its functions, we have characterized the phenotypic properties of Kai1/Cd82 deleted mice, including viability, fertility, lymphocyte composition, blood chemistry and tissue histopathology, and of their wild-type and heterozygote littermates. Interestingly, Kai1/Cd82(-/-) showed no obvious genotype associated defects in any of these processes and displayed no genotype associated histopathologic abnormalities after 12 or 18 months of life. Expression profiles of non-immortal, wild-type and Kai1/Cd82(-/-) mouse embryo fibroblast (MEFs) indicated distinct sex-specific and genotype-specific profiles. These data identify 191 and 1,271 differentially expressed transcripts (by twofold at P < 0.01) based on Kai1/CD82 genotype status in female and male MEFs, respectively. Differentially expressed genes in male MEFs were surprisingly enriched for cell division related processes, suggesting that Kai1/Cd82 may functionally affect these processes. This suggests that Kai/Cd82 has an unappreciated role in the early establishment of proliferation and division when challenged with a new environment that might play a role in adaptability to new metastatic sites.Entities:
Keywords: CD82; gene knockout; metastasis suppressor
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Year: 2013 PMID: 23401136 PMCID: PMC7706324 DOI: 10.1002/mc.22009
Source DB: PubMed Journal: Mol Carcinog ISSN: 0899-1987 Impact factor: 4.784