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Aberrant methylation of the Vimentin gene in hepatocellular carcinoma.
Kitamura, Yohei; Shirahata, Atsushi; Sakuraba, Kazuma; Goto, Tetsuhiro; Mizukami, Hiroki; Saito, Mitsuo; Ishibashi, Kazuyoshi; Kigawa, Gaku; Nemoto, Hiroshi; Sanada, Yutaka; Hibi, Kenji.
Afiliação
  • Kitamura Y; Gastroenterological Surgery, Showa University Fujigaoka Hospital, Yokohama, Japan.
Anticancer Res ; 31(4): 1289-91, 2011 Apr.
Article em En | MEDLINE | ID: mdl-21508377
BACKGROUND: Recently, it was shown that the Vimentin gene, usually activated in mesenchymal cells, was highly methylated in colorectal carcinoma. MATERIALS AND METHODS: The methylation status of the Vimentin gene was examined in primary carcinomas and the corresponding normal tissues derived from 43 patients with hepatocellular carcinoma (HCC) using quantitative methylation-specific PCR (qMSP) and the correlation between the methylation status and the clinicopathological findings was evaluated. RESULTS: Aberrant methylation of the Vimentin gene was detected in 24 out of the 43 (56%) primary HCC. This result suggested that the aberrant methylation of the Vimentin gene was frequent in HCC. Subsequently, clinicopathological data were correlated with the methylation status. A significant difference was observed in the value of alpha-fetoprotein (AFP) (p=0.045), maximal tumor size (p=0.048) and TNM stage (p=0.043) between the methylation-positive and -negative cases. CONCLUSION: Aberrant methylation of Vimetin might be an early event in the course of hepatocarcinogenesis.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vimentina / Regulação Neoplásica da Expressão Gênica / Carcinoma Hepatocelular / Metilação de DNA / Neoplasias Hepáticas Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: Anticancer Res Ano de publicação: 2011 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vimentina / Regulação Neoplásica da Expressão Gênica / Carcinoma Hepatocelular / Metilação de DNA / Neoplasias Hepáticas Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: Anticancer Res Ano de publicação: 2011 Tipo de documento: Article