Delayed reproductive death as a dominant phenotype in cell clones surviving x-irradiation

Wushou P. Chang, John B. Little

Research output: Contribution to journalArticlepeer-review

86 Citations (Scopus)

Abstract

Residual damage manifested as reduced cloning efficiency was observed in many of the cloned progeny of Chinese hamster ovary (CHO) cells and human carcinoma SQ-20B cells surviving X-irradiation. This stable phenotype, which we have termed delayed reproductive death, persisted for >50 generations of cell replication post-irradiation. Clones showing this phenotype were aneuploid, and formed colonies with a high proportion of giant cells. By somatic cell hybridization of CHO clones, the delayed reproductive death phenotype was found to be a dominant trait; the cloning efficiency of hybrid clones was persistently depressed, as compared with that of control hybrid cells. These results suggest that delayed reproductive death represents a specific cellular response that may persist in some of the progeny of mammalian cells for long periods after X-irradiation.

Original languageEnglish
Pages (from-to)923-928
Number of pages6
JournalCarcinogenesis
Volume13
Issue number6
DOIs
Publication statusPublished - Jun 1992
Externally publishedYes

ASJC Scopus subject areas

  • Cancer Research

Fingerprint

Dive into the research topics of 'Delayed reproductive death as a dominant phenotype in cell clones surviving x-irradiation'. Together they form a unique fingerprint.

Cite this