Identification and characterization of a novel germ line p53 mutation in familial gastric cancer in the Japanese population

• Published in: Carcinogenesis (New York) 2007-09, Vol.28 (9), p.2013-2018
• Main Authors: Yamada, Hidetaka, Shinmura, Kazuya, Okudela, Koji, Goto, Masanori, Suzuki, Masaya, Kuriki, Ken, Tsuneyoshi, Toshihiro, Sugimura, Haruhiko
• Format: Article
• Language: English
• Subjects: Amino Acid Substitution; Biological and medical sciences; Carcinogenesis, carcinogens and anticarcinogens; Cell Division; Cell Line, Tumor; Doxycycline - pharmacology; Female; Fluorescent Antibody Technique, Indirect; Gastroenterology. Liver. Pancreas. Abdomen; Genes, p53; Germ-Line Mutation; Humans; Japan - epidemiology; Li-Fraumeni Syndrome - epidemiology; Li-Fraumeni Syndrome - genetics; Male; Medical sciences; Mutation, Missense; Pedigree; Plasmids; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Stomach Neoplasms - epidemiology; Stomach Neoplasms - genetics; Stomach Neoplasms - pathology; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumor Suppressor Protein p53 - genetics; Tumors
• ISSN: 0143-3334; 1460-2180
• DOI: 10.1093/carcin/bgm175

Germ line mutations of the p53 gene are known to cause Li-Fraumeni syndrome, and a germ line p53 mutation has recently been reported in a small subset of familial gastric cancer (FGC) in Europe and Korea. Although the incidence of gastric cancer is very high in Japan and familial clustering is not uncommon, there has been little information on the genetic factors of FGC. Therefore, to determine the role of germ line p53 mutations in FGC in the Japanese population in this study, we used sequencing analysis to examine 80 individuals from 35 Japanese FGC families without germ line CDH1 mutations for germ line p53 mutations. One missense (c.91G>A: p.Val31Ile) and two intronic germ line mutations were found, and transcriptional activity of the Ile31 mutant on p53-responsive genes was examined to determine the functional effect of the novel p.Val31Ile germ line mutation. A luciferase reporter assay showed that the transcriptional activity of p21 (CDKN1A) and MDM2 promoters but not of the BAX promoter was significantly lower in the Ile31-type p53 than in the wild-type (wt) p53. Next, doxycycline-regulated p53-inducible H1299 cell lines were established by applying a retrovirus-mediated gene transfer system to a p53-null human H1299 cell line. Under similar p53 expression conditions shown by western blot and immunofluorescence analyses, a cell proliferation assay showed that the Ile31-type p53 had significantly lower cell proliferation suppressing activity than wt p53. These results suggest that Ile31-type p53 may be partly involved in FGC because of its low transcriptional activity and low cell proliferation suppressing activity.