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PMID: 6861150 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Unilateral chromatid damage: a new basis for 6-thioguanine cytotoxicity.

Cancer research ·Vol. 43 ·No. 8 ·1983-08-00 ·Pages 3852-6

Maybaum J, Mandel HG

Abstract

Using the technique of premature chromosome condensation, which permits the visual inspection of interphase chromatin, we have shown previously that 28 hr after exposure to 6-thioguanine (TG) specific and drastic morphological changes in the chromosomes of Chinese hamster ovary fibroblasts in the G2 phase of the cell cycle become evident. In this paper, we demonstrate that this damage is a dose-related effect, appearing as sharp curling or "kinking" at lower TG concentrations and as unilateral chromatid damage and gross chromosome disruption at higher TG concentrations. With the use of a scoring system for quantitating the severity of this specific damage, the threshold concentrations for the appearance of unilateral chromatid damage and for loss of colony-forming ability were shown to be identical. Since the appearance of unilateral chromatid damage paralleled the appearance of TG-induced cytotoxicity in terms of time and dose, and since the severe disruption of G2 prematurely condensed chromosomes is consistent with TG-induced G2 arrest seen in this and other systems, we conclude that unilateral chromatid damage is centrally involved in the delayed cytotoxicity of TG in Chinese hamster ovary cells.

MeSH Terms
Animals Cell Cycle Cell Survival/drug effects Chromatids/drug effects Cricetinae Cricetulus Dose-Response Relationship, Drug Female Ovary/drug effects Thioguanine/toxicity
Chemicals
Thioguanine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Maybaum J
Mandel H G
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1983-08-00
Pages
3852-6
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · 5T-32-CA09223 · United States
NCI NIH HHS · CA02978 · United States
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