ENHANCED CHROMATID DAMAGE IN BLOOD-LYMPHOCYTES AFTER G2 PHASE-X IRRADIATION, A MARKER OF THE ATAXIA-TELANGIECTASIA GENE

被引:84
作者
SANFORD, KK
PARSHAD, R
PRICE, FM
JONES, GM
TARONE, RE
EIERMAN, L
HALE, P
WALDMANN, TA
机构
[1] NCI,BIOSTAT BRANCH,BETHESDA,MD 20205
[2] NCI,METAB BRANCH,BETHESDA,MD 20205
[3] HOWARD UNIV,COLL MED,DEPT PATHOL,WASHINGTON,DC 20001
[4] UNIV MED & DENT NEW JERSEY,DEPT PEDIAT,NEW BRUNSWICK,NJ
关键词
D O I
10.1093/jnci/82.12.1050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
An assay for ataxia-telangiectasia (A-T) heterozygotes, i.e., healthy carriers of the A-T gene(s), requiring only a small sample (3.5 mL) of peripheral blood, is described. Frequencies of chromatid aberrations in phytohemagglutinin-stimulated blood lymphocytes collected by demecolcine from 0.5 hour to 1.5 hours after x irradiation with 58 roentgens were twofold to threefold higher in A-T heterozygotes than in clinically normal controls and twofold to threefold higher in A-T patients (homozygotes) than in A-T gene carriers. The persistence of chromatid breaks and gaps in lymphocytes following radiation-induced DNA damage during G2 suggests a deficiency or deficiencies in DNA repair that may be the defect at the molecular level that results in the enhanced radiosensitivity and cancer proneness characterizing A-T gene carriers and patients. [J Natl Cancer Inst 82:1050-1054, 1990] © 1990 Oxford University Press.
引用
收藏
页码:1050 / 1054
页数:5
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