Your browser doesn't support javascript.
loading
5-Azacytidine (5-aza) Induces p53-associated Cell Death Through Inhibition of DNA Methyltransferase Activity in Hep3B and HT-29 Cells.
Kim, Dae-Yeon; Lee, Rangyeon; Cheong, Hee-Tae; Ra, Chang-Six; Rhee, Ki-Jong; Park, Jeongho; Jung, Bae Dong.
Afiliação
  • Kim DY; College of Veterinary Medicine & Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
  • Lee R; College of Veterinary Medicine & Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
  • Cheong HT; College of Veterinary Medicine & Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
  • Ra CS; College of Animal Life Sciences, Kangwon National University, Chuncheon, Republic of Korea.
  • Rhee KJ; Department of Biomedical Laboratory Science, College of Health Sciences, Yonsei University at Wonju, Wonju, Republic of Korea.
  • Park J; College of Veterinary Medicine & Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea; jhp@kangwon.ac.kr.
  • Jung BD; College of Veterinary Medicine & Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea; bdjung@kangwon.ac.kr.
Anticancer Res ; 43(2): 639-644, 2023 Feb.
Article em En | MEDLINE | ID: mdl-36697082
BACKGROUND/AIM: DNA methylation regulates the expression of genes that control mechanisms of cell death. TP53 gene expression inhibits tumorigenesis, and its action is closely associated with cell death. 5-Azacytidine (5-aza), increases the expression of the TP53 gene by inhibiting DNA methyltransferase. MATERIALS AND METHODS: Using 5-aza, we induced DNA hypomethylation in p53-null and p53-expressing cancer cell lines and investigated potential mechanisms of cancer cell death. RESULTS: TP53 expression promoted cell death. Notably, methylation-specific PCR (MSP) and bisulfite sequencing revealed more methylation sites at the TP53 promoter region in p53-null cells than in p53-expressing cells. CONCLUSION: This study suggests a novel mechanism of tumorigenesis regulated by p53 expression.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Azacitidina / Proteína Supressora de Tumor p53 Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Azacitidina / Proteína Supressora de Tumor p53 Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article