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Title: Effects of various chemical agents on sister chromatid exchanges, chromosome aberrations, and DNA repair in normal and abnormal human lymphoid cell lines

Journal Article · · J. Natl. Cancer Inst.; (United States)
OSTI ID:6530225

Cells from a line (SN1029) derived from a case of chronic lymphocytic leukemia (CLL) were highly sensitive to the killing effects of 4-nitroquinoline 1-oxide (4-NQO), methyl methanesulfonate, ethyl methanesulfonate (EMS), mitomycin C (MMC), daunomycin (DM), bleomycin, and cytosine arabinoside, as compared to the lack of sensitivity of a normal lymphocytic cell line treated with these agents. Cells treated with N-methyl-N'-nitro-N-nitronitrosoguanidine (MNNG) were a possible exception to this pattern. Among the chemicals tested, SN1029 cells were extremely sensitive to MMC with regard to frequency of sister chromatid exchange(s) (SCE), even though MMC did not greatly increase the incidence of chromosome aberrations. Reverse results were obtained with the 6 other chemicals. Unscheduled DNA synthesis (USD) in normal and SN1029 cells was examined following uv radiation (200 ergs/mm/sup 2/) and treatments with EMS, MNNG, MMC, and 4-NQO for 90 min at 6.0 ..mu..g/ml (expt I) and for 48 hrs at 0.003, 0.03, 0.3, and 6.0 ..mu..g/ml (expt II). Almost no detectable levels of USD were seen with MMC in experiment I or with MMC, EMS, MNNG, and 4-NQO in experiment II, whereas USD did occur following 4-NQO in experiment II, whereas USD did occur following 4-NGO, EMS, MNNG, and uv radiation in experiment I. Comparison of SCE breakpoints and USD indicated that the SCE breakpoints within chromosome No. 1 in MMC- and 4-NQO-treated normal cells were nonrandom. The results indicate that SCE and excision repair are not closely linked and that the high SCE sensitivity and cell death ofthe CLL cell line are independent of the quantitative capacity for excision repair.

Research Organization:
Roswell Park Memorial Inst., Buffalo, NY
OSTI ID:
6530225
Journal Information:
J. Natl. Cancer Inst.; (United States), Vol. 62:1
Country of Publication:
United States
Language:
English

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