Immortalization of cultured human fibroblasts with the mutant p53 gene and X‐rays

M. Namba*, K. Mihara, T. Kondo, Y. Inoue, T. Tsuji, K. Fushimi, T. Shima, M. Iijima

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

The mutant p53 gene (mp53; codon 273Arg‐His) was introduced into normal human fibroblasts (OUMS‐24 strain), and a G418‐resistant clone, OUMS‐24/P6, was obtained. This clone expressed mp53 and showed an extended life span, but it senesced at the 79th population‐doubling level (PDL). When these cells were subjected to eight intermittent treatments with 2 Gy of x‐rays, they were immortalized, whereas normal fibroblasts (OUMS‐24) into which mp53 had not been introduced were not immortalized by the same x‐ray treatment. These results indicate that the introduction of mp53 alone is not sufficient for immortalization of human cells and that mutations of the remaining wild‐type p53 or other genes are also necessary. © 1995 Wiley‐Liss, Inc.

Original languageEnglish (US)
Pages (from-to)294-298
Number of pages5
JournalRadiation Oncology Investigations
Volume3
Issue number6
DOIs
StatePublished - 1995

Keywords

  • human fibroblasts
  • immortalization
  • mutant p53
  • x‐rays

ASJC Scopus subject areas

  • Radiological and Ultrasound Technology
  • Radiation
  • Oncology
  • Radiology Nuclear Medicine and imaging

Fingerprint Dive into the research topics of 'Immortalization of cultured human fibroblasts with the mutant p53 gene and X‐rays'. Together they form a unique fingerprint.

Cite this