Absence of p51 mutation in human hepatocellular carcinoma

Cancer Lett. 2000 Feb 1;148(2):161-4. doi: 10.1016/s0304-3835(99)00330-4.

Abstract

The p51 gene encodes a protein with significant homology to p53. To investigate the involvement of the p51 gene in human hepatocarcinogenesis, mutation analysis of the p51 gene was performed in 54 cases of hepatocellular carcinoma (HCC). No mutations causing amino acid substitutions or frameshifts were found by polymerase chain reaction-single strand conformational polymorphism (PCR-SSCP) analysis of the entire coding region. The result indicated that mutation of the p51 gene does not play a major role in the development of HCC in Japanese patients. Further studies on p51 expression and its functions, including the interaction with p53, are necessary to elucidate the role of the p51 gene in human hepatocarcinogenesis.

MeSH terms

  • Carcinoma, Hepatocellular / genetics*
  • DNA-Binding Proteins / genetics*
  • Genes, Tumor Suppressor
  • Humans
  • Liver Neoplasms / genetics*
  • Mutation*
  • Phosphoproteins*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / genetics
  • Polymorphism, Single-Stranded Conformational
  • RNA Splicing
  • Trans-Activators*
  • Transcription Factors
  • Tumor Cells, Cultured
  • Tumor Suppressor Proteins

Substances

  • DNA-Binding Proteins
  • Phosphoproteins
  • TP63 protein, human
  • Trans-Activators
  • Transcription Factors
  • Tumor Suppressor Proteins