• Title of article

    Absence of p16, p21 and p53 gene alterations in hepatocellular carcinomas induced by N-nitrosodiethylamine or a choline-deficient l-amino acid-defined diet in rats

  • Author/Authors

    Sasaki، نويسنده , , Yasutaka and Tsujiuchi، نويسنده , , Toshifumi and Murata، نويسنده , , Nao and Kubozoe، نويسنده , , Tadahiko and Tsutsumi، نويسنده , , Masahiro and Konishi، نويسنده , , Yoichi، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2000
  • Pages
    7
  • From page
    71
  • To page
    77
  • Abstract
    To clarify the involvement of tumor suppressor genes in exogenous and endogenous liver carcinogenesis, alterations of p16, p21 and p53 in hepatocellular carcinomas (HCCs) induced by N-nitrosodiethylamine (DEN) and a choline deficient l-amino acid-defined (CDAA) diet in rats were investigated. Male Fischer 344 rats received DEN at 6-week of age followed by partial hepatectomy (PH), with colchicine to induce cell cycle disturbance, and a selection pressure regimen. Sacrifice was after 42 weeks. Other animals continuously received a CDAA diet for 75 weeks and were then killed. Eleven and 15 HCCs were obtained, respectively. Total RNA was extracted from and cDNA was synthesized with reverse transcriptase to allow investigation of mutations in p16, p21 and p53 by polymerase chain reaction single strand conformation polymorphism (PCR-SSCP) analysis. Expression of p16 and p21 mRNA was also analyzed by reverse transcription (RT)-PCR. The results showed no mutations or deletions of p16, p21 and p53 in any of the HCCs induced by DEN or CDAA. Loss or decrease of p16 and p21 expression were also not found, suggesting that p16, p21 and p53 alteration may not be necessary for either exogenous or endogenous liver carcinogenesis in rats.
  • Keywords
    hepatocellular carcinoma , N-nitrosodiethylamine , Rat , Choline-deficient l-amino acid-defined diet , Tumor suppressor gene
  • Journal title
    Cancer Letters
  • Serial Year
    2000
  • Journal title
    Cancer Letters
  • Record number

    1801191