Sensitivity to genotoxic effects of bleomycin in humans: Possible relationship to environmental carcinogenesis

Responses to the genotoxic effect of bleomycin in lymphocytes of blood cultures, expressed as the average number of chromatid breaks per cell (b/c), varied from less than 0.20 to more than 2.00 in 335 normal individuals. More than 11% of the subjects tested showed a b/c rate above 1.00 and more than 22% showed a b/c rate above 0.80. These individuals are considered sensitive to this radiomimetic drug. The distributional profile of bleomycin responses of the control individuals appears to be representative of the normal human population. In patients with cancers of the colon (83), upper aerodigestive tract (head/neck) (77), and lung (71), the frequencies of subjects in the hypersensitive class were found to be between 40 and 50%, and the response profiles were distinctly different from those of the control population. On the other hand, in a group of elderly cigarette smokers, who exhibited no symptoms of lung cancer, the bleomycin sensitivity profile was significantly skewed toward the more resistant stratum, with only one hypersensitive case among 56 individuals tested (1.78%). The sensitivity profile of patients with breast cancer (82) was similar to that of the control population. Our data suggest that: (1) mutagen sensitivity may play an important role in carcinogenesis of organs and tissues that have direct contact with the external environment (respiratory, digestive, and integumentary systems); (2) it appears to have no significant influence on carcinogenesis of tissues that are not directly exposed to the environment (e.g., breast, brain); and (3) it also has little impact on carcinogenesis in individuals with a hereditary predisposition to cancer (e.g., retinoblastoma, Gardner's syndrome). Development of more effective and precise test systems for carcinogen sensitivity is highly desirable for identification of persons at risk.

[1]  W. Hittelman,et al.  Heterogeneity in chromosome damage and repair rates after bleomycin in ataxia telangiectasia cells. , 1988, Cancer research.

[2]  P C Hanawalt,et al.  Heterogeneous DNA damage and repair in the mammalian genome. , 1987, Cancer research.

[3]  R. Weksberg,et al.  Structural alterations of DNA ligase I in Bloom syndrome. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[4]  J. Mulvihill,et al.  Strategies for controlling cancer through genetics: report of a workshop. , 1987, American journal of human genetics.

[5]  F. Becker,et al.  Altered DNA ligase I activity in Bloom's syndrome cells , 1987, Nature.

[6]  R. Parshad,et al.  Biochemical evidence for deficient DNA repair leading to enhanced G2 chromatid radiosensitivity and susceptibility to cancer. , 1986, Radiation research.

[7]  T. Hsu,et al.  Differential susceptibility to a mutagen among human individuals: synergistic effect on chromosome damage between bleomycin and aphidicolin. , 1986, Anticancer research.

[8]  T. Hsu,et al.  Differential mutagen susceptibility in cultured lymphocytes of normal individuals and cancer patients. , 1985, Cancer genetics and cytogenetics.

[9]  J. Bedford,et al.  X-ray--induced breakage and rejoining of human interphase chromosomes. , 1983, Science.

[10]  Hsu Tc,et al.  Bleomycin-induced chromosome damage in lymphocytes of medullary thyroid carcinoma patients and their family members. , 1983 .

[11]  R. Parshad,et al.  Chromatid damage after G2 phase x-irradiation of cells from cancer-prone individuals implicates deficiency in DNA repair. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[12]  W. Enker,et al.  Reduced capacity for DNA repair synthesis in patients with or genetically predisposed to colorectal cancer. , 1983, Journal of the National Cancer Institute.

[13]  S. Horwitz,et al.  Mechanism of bleomycin action: in vitro studies. , 1981, Life sciences.

[14]  R. Benz,et al.  Sensitivity to five mutagens in Fanconi's anemia as measured by the micronucleus method. , 1978, Cancer research.

[15]  R. Setlow Repair deficient human disorders and cancer , 1978, Nature.

[16]  T. Hsu,et al.  Bleomycin causes release of nucleosomes from chromatin and chromosomes , 1978, Nature.

[17]  K. Kohn,et al.  Effect of pH on the bleomycin-induced DNA single-strand scission in L1210 cells and the relation to cell survival. , 1976, Cancer research.

[18]  K. Kohn,et al.  Single-strand scission and repair of DNA in mammalian cells by bleomycin. , 1976, Cancer research.

[19]  J. Mccormick,et al.  Frequency of ultraviolet light-induced mutations is higher in xeroderma pigmentosum variant cells than in normal human cells , 1976, Nature.

[20]  J. Delhanty,et al.  Unscheduled DNA synthesis, u.v.‐induced chromosome aberrations adn SV40 transformation in cultured cells from xeroderma pigmentosum , 1971, Annals of human genetics.

[21]  A. Knudson Mutation and cancer: statistical study of retinoblastoma. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[22]  R. Setlow,et al.  Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. , 1969, Proceedings of the National Academy of Sciences of the United States of America.

[23]  J. Cleaver Defective Repair Replication of DNA in Xeroderma Pigmentosum , 1968, Nature.

[24]  K. S. Morgan,et al.  SCE and UDS studies in a family with retinoblastoma: a case study. , 1982, Teratogenesis, carcinogenesis, and mutagenesis.

[25]  L. Strong,et al.  A Short-Term Cytogenetic Test for Genetic Instability in Humans , 1981 .

[26]  B. Glickman DNA Repair and its Relationship to the Origins of Human Cancer , 1980 .

[27]  P. Smith,et al.  Ataxia telangiectasia: an inherited human disorder involving hypersensitivity to ionizing radiation and related DNA-damaging chemicals. , 1979, Annual review of genetics.

[28]  C. Arlett,et al.  CELL KILLING AND MUTAGENESIS IN REPAIR-DEFECTIVE HUMAN CELLS , 1978 .