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Mol Carcinog ; 29(3): 143-50, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11108659

RESUMO

We recently limited the location of a candidate tumor suppressor gene in invasive (T3a/b) bladder transitional-cell carcinoma (TCC) to a 2.5-cM region at chromosome 10q23.3. This region harbors the MMAC1/PTEN/TEP1 gene (referred to hereafter as MMAC1), a dual-phosphatase tumor-suppressor gene frequently inactivated in variety of malignant tumors. In the present study, we examined whether MMAC1 is a target for inactivation by mutations and deletions in bladder TCC cell lines and specimens. MMAC1 was inactivated by homozygous deletions and mutations in three (27%) of 11 bladder cancer cell lines. One cell line, UC-3, had homozygous deletions, and two other cell lines, T-24 and UC-9, had missense mutations. T-24 had also a nonsense mutation. However, none of the 33 bladder TCC specimens examined had a mutation or deletion in the coding region. These results suggest that MMAC1 is not the primary target for inactivation in bladder TCC and that another gene, in close proximity to the MMAC1 locus, within this region of frequent allelic losses, may be the target for inactivation.


Assuntos
Carcinoma de Células de Transição/genética , Regulação Neoplásica da Expressão Gênica , Inativação Gênica , Monoéster Fosfórico Hidrolases/genética , Proteínas Supressoras de Tumor , Neoplasias da Bexiga Urinária/genética , Carcinoma de Células de Transição/metabolismo , Análise Mutacional de DNA , Éxons , Deleção de Genes , Rearranjo Gênico , Humanos , Mutação , PTEN Fosfo-Hidrolase , Monoéster Fosfórico Hidrolases/biossíntese , Polimorfismo Conformacional de Fita Simples , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Células Tumorais Cultivadas , Neoplasias da Bexiga Urinária/metabolismo
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