Literature DB >> 7317030

Effect of partial hepatectomy on removal of O6-methylguanine from alkylated DNA by rat liver extracts.

A E Pegg, W Perry, R A Bennett.   

Abstract

1. The activity of an enzyme catalysing the loss of O6-methylguanine from methylated DNA was increasing during liver regeneration after partial hepatectomy. Activity was increased 3-fold by 24h and was maximal (6-fold increase) over the period 48-72h after operation. 2. This activity could also be induced by chronic treatment with dimethylnitrosamine, but the maximal response amounted to a 2-3-fold change (with the greater effect in male rats) after 4-6 weeks of exposure to daily doses of 2 mg of dimethylnitrosamine/kg. 3. Neither partial hepatectomy nor treatment with dimethylnitrosamine increased the activities of two other enzymes repairing alkylated DNA, DNA (7-methylguanine-)glycosylase and DNA (3-methyladenine-)glycosylase. 4. These results therefore indicate that there is a selective induction of the O6-methylguanine removal system during hepatocyte proliferation. Since this product is known to lead to mutations and its persistence in DNA throughout cell replication has been implicated in tumour initiation, this induction may play a role in resistance to carcinogenesis by alkylating agents.

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Year:  1981        PMID: 7317030      PMCID: PMC1163070          DOI: 10.1042/bj1970195

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  37 in total

Review 1.  Xeroderma pigmentosum: biochemical and genetic characteristics.

Authors:  J E Cleaver; D Bootsma
Journal:  Annu Rev Genet       Date:  1975       Impact factor: 16.830

2.  Quantitation of the adaptive response to alkylating agents.

Authors:  P Robins; J Cairns
Journal:  Nature       Date:  1979-07-05       Impact factor: 49.962

3.  Effect of a single treatment with the alkylating carcinogens dimethynitrosamine, diethylnitrosamine and methyl methanesulphonate, on liver regenerating after partial hepatectomy. I. Test for induction of liver carcinomas.

Authors:  V M Craddock
Journal:  Chem Biol Interact       Date:  1975-05       Impact factor: 5.192

4.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

Review 5.  Formation and metabolism of alkylated nucleosides: possible role in carcinogenesis by nitroso compounds and alkylating agents.

Authors:  A E Pegg
Journal:  Adv Cancer Res       Date:  1977       Impact factor: 6.242

6.  A new pathway for DNA repair in Escherichia coli.

Authors:  L Samson; J Cairns
Journal:  Nature       Date:  1977-05-19       Impact factor: 49.962

Review 7.  Some chemical aspects of dose-response relationships in alkylation mutagenesis.

Authors:  P D Lawley
Journal:  Mutat Res       Date:  1974-06       Impact factor: 2.433

8.  Repair of DNA damaged by alkylating carcinogens is defective in xeroderma pigmentosum-derived fibroblasts.

Authors:  R Goth-Goldstein
Journal:  Nature       Date:  1977-05-05       Impact factor: 49.962

9.  DNA excision-repair deficiency of human peripheral blood lymphocytes treated with chemical carcinogens.

Authors:  D Scudiero; A Norin; P Karran; B Strauss
Journal:  Cancer Res       Date:  1976-04       Impact factor: 12.701

10.  Enzymatic release of 7-methylguanine from methylated DNA by rodent liver extracts.

Authors:  G P Margison; A E Pegg
Journal:  Proc Natl Acad Sci U S A       Date:  1981-02       Impact factor: 11.205

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  23 in total

Review 1.  DNA adducts and cell cycle.

Authors:  H M Rabes
Journal:  J Cancer Res Clin Oncol       Date:  1986       Impact factor: 4.553

2.  O6-Methylguanine repair of methylated DNA in vitro: cell cycle-dependence of rat liver methyltransferase activity.

Authors:  C Schuster; G Rode; H M Rabes
Journal:  J Cancer Res Clin Oncol       Date:  1985       Impact factor: 4.553

3.  Adaptive resynthesis of O6-methylguanine-accepting protein can explain the differences between mammalian cells proficient and deficient in methyl excision repair.

Authors:  E A Waldstein; E H Cao; R B Setlow
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

4.  Cell-specific differences in O6-alkylguanine DNA repair activity during continuous exposure to carcinogen.

Authors:  J A Swenberg; M A Bedell; K C Billings; D R Umbenhauer; A E Pegg
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

5.  Isolation and characterization of monoclonal antibodies directed against the DNA repair enzyme uracil DNA glycosylase from human placenta.

Authors:  P Arenaz; M A Sirover
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

6.  Cloning and characterization of the Salmonella typhimurium ada gene, which encodes O6-methylguanine-DNA methyltransferase.

Authors:  A Hakura; K Morimoto; T Sofuni; T Nohmi
Journal:  J Bacteriol       Date:  1991-06       Impact factor: 3.490

7.  Modification of N-methyl-N-nitrosourea-induced urinary bladder carcinogenesis in rats following stimulation of urothelial proliferation by a partial cystectomy.

Authors:  E Kunze; G Gassner
Journal:  J Cancer Res Clin Oncol       Date:  1986       Impact factor: 4.553

8.  Effect of N-nitrosamines carcinogenic for oesophagus on O6-alkyl-guanine-DNA-methyl transferase in rat oesophagus and liver.

Authors:  V M Craddock; A R Henderson
Journal:  J Cancer Res Clin Oncol       Date:  1986       Impact factor: 4.553

9.  O4-ethyldeoxythymidine, but not O6-ethyldeoxyguanosine, accumulates in hepatocyte DNA of rats exposed continuously to diethylnitrosamine.

Authors:  J A Swenberg; M C Dyroff; M A Bedell; J A Popp; N Huh; U Kirstein; M F Rajewsky
Journal:  Proc Natl Acad Sci U S A       Date:  1984-03       Impact factor: 11.205

10.  Inhibitory effect of partial cystectomy on experimental carcinogenesis in the urinary bladder.

Authors:  E Kunze; H H Wöltjen; U Niemann
Journal:  J Cancer Res Clin Oncol       Date:  1983       Impact factor: 4.553

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