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Heterogeneity in the clastogenic response to x-rays in lymphocytes from Ataxia-telangiectasia heterozygotes and controls.

Authors
Wiencke-JK; Wara-DW; Little-B; Kelsey-KT
Source
Cancer Causes Control 1992 May; 3(3):237-245
NIOSHTIC No.
20000997
Abstract
A coded analysis of X-ray-induced chromatid aberrations in lymphocyte cultures from 45 control individuals and 19 ataxia-telangiectasia (A-T) heterozygotes was performed. The distribution of chromatid breaks induced in the late G2 portion of the cell cycle by 60 cGy of X-rays appeared bimodal in the study population. In six controls (13 percent) and in 12 of 19 (63 percent) A-T heterozygotes, the yields of X-ray-induced breaks observed were within the higher mode of the distribution. However, lymphocytes from A-T heterozygotes sensitive to the induction of chromatid breaks by 60 cGy did not contain increased numbers of aberrations following exposure to 20 cGy. The radio-resistant inhibition of DNA synthesis that occurs in A-T homozygotes was not observed in heterozygotes. Co-cultivation experiments showed an increased G2 delay in lymphocytes from an A-T heterozygote whose lymphocytes contained increased X-ray-induced chromatid breaks. The results show a significant association of A-T heterozygosity with G2 chromosomal sensitivity (P less than 0.001; Wilcoxon rank sum test). The measurement of X-ray-induced breaks, however, failed to identify 37 percent of A-T heterozygotes tested. The predicted prevalence of increased sensitivity to X-rays in controls is approximately three- to 30-fold greater than the estimated frequency of A-T heterozygotes in the general population. Therefore, although the increased sensitivity to X-ray-induced chromatid breaks appears to be associated with the A-T-gene, it is not a reliable indicator of A-T heterozygosity. Genetic or environmental factors other than the A-T gene also must be involved in the increased clastogenic response.
Keywords
Mutagenesis; Humans; Environmental-factors; Genetics; DNA-damage
Contact
Department of Epidemiology and Biostatistics, School of Medicine, University of California, San Francisco 94143
CODEN
CCCNEN
Publication Date
19920501
Document Type
Journal Article
Funding Amount
162000
Funding Type
Grant
Fiscal Year
1992
NTIS Accession No.
NTIS Price
Identifying No.
Grant-Number-K01-OH-00110
Issue of Publication
3
ISSN
0957-5243
NIOSH Division
OD
Priority Area
Cancer
Source Name
Cancer Causes and Control
State
MA; CA
Performing Organization
Harvard University, School of Public Health, Occupational Health Program, Boston, Massachusetts
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