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Cancer Genet Cytogenet ; 144(1): 80-2, 2003 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-12810262

RESUMO

Colorectal cancer (CRC) and breast cancer constitute common neoplasms in Western countries and leading causes of cancer-related death. Development and progression of both malignancies occur as a multistep process, requiring the activation of oncogenes and the inactivation of several tumor suppressor genes. Our group has recently identified a minimal region of deletion on 22q13 involved in CRC and breast cancer patients, which is highly indicative of the existence of a tumor suppressor gene (or genes). We performed mutation analysis of the PARVG gene, one of the genes present on the 22q13 region of interest, which has been previously demonstrated to have a reduced expression in some cancer cell lines. We have identified several DNA variants that are not compatible with pathogenic mutations. Accordingly, PARVG appears not to be a tumor suppressor gene involved in CRC and breast cancer development and progression.


Assuntos
Neoplasias da Mama/genética , Cromossomos Humanos Par 22 , Neoplasias Colorretais/genética , Genes Supressores de Tumor , Sequência de Bases , Primers do DNA , Feminino , Humanos , Mutação , Polimorfismo Conformacional de Fita Simples
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