Literature DB >> 3086210

Adaptation-like response to the chemical induction of sister chromatid exchanges in human lymphocytes.

K Morimoto, M Sato-Mizuno, A Koizumi.   

Abstract

Experiments have been performed to determine whether human lymphocytes in primary cultures can show an "adaptive" response to the induction of cellular lesions (manifested as a production of sister chromatid exchanges, SCEs) as previously found in bacteria and established human and mammalian cell lines. Human lymphocytes were pretreated with various subtoxic concentrations (5-50 ng/ml) of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) once every 6h for 72 h, and subsequently challenged by a high dose (4 micrograms/ml) of MNNG. The lymphocytes in MNNG-challenged cultures had the lowest frequency of SCEs when pretreated with 10 ng/ml MNNG. Further cross-resistance study revealed that repeated pretreatments of lymphocytes with 10 ng/ml MNNG for 72 h can render the cells resistant to the induction of SCEs by the following challenge with a high dose of MNNG, but not of mitomycin C or ethyl nitrosourea. The data also suggest variations in the degree of the adaptation-like response among individuals.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3086210     DOI: 10.1007/bf00292670

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  35 in total

Review 1.  Enzymatic repair of DNA.

Authors:  L Grossman; A Braun; R Feldberg; I Mahler
Journal:  Annu Rev Biochem       Date:  1975       Impact factor: 23.643

2.  Adaptive response of human lymphocytes to low concentrations of radioactive thymidine.

Authors:  G Olivieri; J Bodycote; S Wolff
Journal:  Science       Date:  1984-02-10       Impact factor: 47.728

3.  Adaptation to alkylation resistance involves the induction of a DNA glycosylase.

Authors:  G Evensen; E Seeberg
Journal:  Nature       Date:  1982-04-22       Impact factor: 49.962

4.  Use of a reversion assay HGPRT- to HGPRT+ to demonstrate mutagenic adaptation in V79 Chinese hamster cells.

Authors:  M Fox; C M Carlton
Journal:  Carcinogenesis       Date:  1984-11       Impact factor: 4.944

5.  Effect of chronic treatment of rats with dimethylnitrosamine on the removal of O6-methylguanine from DNA.

Authors:  R Montesano; H Brésil; G Planche-Martel; G P Margison; A E Pegg
Journal:  Cancer Res       Date:  1980-02       Impact factor: 12.701

6.  Enhanced survival and reduced mutation and aberration frequencies induced in V79 chinese hamster cells pre-exposed to low levels of methylating agents.

Authors:  B Kaina
Journal:  Mutat Res       Date:  1982-03       Impact factor: 2.433

7.  Enzymatic repair of premutagenic DNA lesions in human epidermis. Quantitation of O6-methylguanine-DNA methyltransferase and uracil-DNA glycosylase activities.

Authors:  B Myrnes; G Eggset; G Volden; H Krokan
Journal:  Mutat Res       Date:  1984 Mar-Apr       Impact factor: 2.433

8.  Pretreatment of Chinese hamster v79 cells with MNU increases survival without affecting DNA repair or mutagenicity.

Authors:  L G Durrant; G P Margison; J M Boyle
Journal:  Carcinogenesis       Date:  1981       Impact factor: 4.944

9.  Abilities of extracts of human lymphocytes to remove O6-methylguanine from DNA.

Authors:  E A Waldstein; E H Cao; M A Bender; R B Setlow
Journal:  Mutat Res       Date:  1982-08       Impact factor: 2.433

10.  Removal of O6-methylguanine from DNA of normal and xeroderma pigmentosum-derived lymphoblastoid lines.

Authors:  R Sklar; B Strauss
Journal:  Nature       Date:  1981-01-29       Impact factor: 49.962

View more
  1 in total

1.  Adaptive response and split-dose effect of radiation on the survival of mice.

Authors:  Ashu Bhan Tiku; R K Kale
Journal:  J Biosci       Date:  2004-03       Impact factor: 1.826

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.