Literature DB >> 6652869

Interindividual variation in the activity of O6-methyl guanine-DNA methyltransferase and uracil-DNA glycosylase in human organs.

B Myrnes, K E Giercksky, H Krokan.   

Abstract

As a step towards understanding the significance of DNA repair enzymes in the protection against genotoxic and carcinogenic agents, we have examined the activity of O6-methyl-guanine-DNA methyltransferase and uracil-DNA glycosylase in adult human liver, stomach, small intestine and colon. Liver had on average a 5- to 8-fold higher activity of O6-MeG-DNA methyltransferase than the other organs and showed about an 8-fold inter-individual variation. In colon and small intestine an even larger inter-individual variation was observed (10- and 40-fold, respectively). In two colon tumors examined the activity of O6-MeG-DNA methyltransferase was several fold higher than in non-neoplastic colon mucosa from the same individuals, while uracil-DNA glycosylase activity was essentially equal in neoplastic and non-neoplastic tissues. O6-MeG-DNA methyltransferase activities in two gastric tumors examined were not higher than in average non-neoplastic tissue. In general the activity of uracil-DNA glycosylase did not correlate with the O6-MeG-DNA methyltransferase activity. The inter-individual variation of this enzyme in the activity was only 3-fold in liver and normal stomach, but varied 5.5 and 60-fold in colon and small intestine, respectively. In conclusion, we have found that O6-MeG-DNA methyltransferase as well as uracil-DNA glycosylase activity vary considerably between different tissues as well as between different individuals. Whether this variation has a genetic basis or reflects variation in 'life style' is not known.

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Year:  1983        PMID: 6652869     DOI: 10.1093/carcin/4.12.1565

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  23 in total

1.  Direct assay for O6-methylguanine-DNA methyltransferase and comparison of detection methods for the methylated enzyme in polyacrylamide gels and electroblots.

Authors:  G N Major; E J Gardner; P D Lawley
Journal:  Biochem J       Date:  1991-07-01       Impact factor: 3.857

2.  Repair of O6-ethylguanine in DNA protects rat 208F cells from tumorigenic conversion by N-ethyl-N-nitrosourea.

Authors:  J Thomale; N H Huh; P Nehls; G Eberle; M F Rajewsky
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

Review 3.  Base excision repair capacity in informing healthspan.

Authors:  Boris M Brenerman; Jennifer L Illuzzi; David M Wilson
Journal:  Carcinogenesis       Date:  2014-10-29       Impact factor: 4.944

4.  Inter-individual variation in DNA repair capacity: a need for multi-pathway functional assays to promote translational DNA repair research.

Authors:  Zachary D Nagel; Isaac A Chaim; Leona D Samson
Journal:  DNA Repair (Amst)       Date:  2014-04-26

Review 5.  Use of cultured human tissues and cells in carcinogenesis research.

Authors:  E W Gabrielson; C C Harris
Journal:  J Cancer Res Clin Oncol       Date:  1985       Impact factor: 4.553

6.  In vivo measurements of interindividual differences in DNA glycosylases and APE1 activities.

Authors:  Isaac A Chaim; Zachary D Nagel; Jennifer J Jordan; Patrizia Mazzucato; Le P Ngo; Leona D Samson
Journal:  Proc Natl Acad Sci U S A       Date:  2017-11-09       Impact factor: 11.205

7.  Requirement for uracil-DNA glycosylase during the transition to late-phase cytomegalovirus DNA replication.

Authors:  C T Courcelle; J Courcelle; M N Prichard; E S Mocarski
Journal:  J Virol       Date:  2001-08       Impact factor: 5.103

8.  Expression of O-Alkylguanine-DNA Alkyltransferase in Normal and Malignant Bladder Tissue of Egyptian Patients.

Authors:  Abir A Saad; Heba Sh Kassem; Andrew C Povey; Geoffrey P Margison
Journal:  J Nucleic Acids       Date:  2010-10-17

9.  Cell cycle regulation and in vitro hybrid arrest analysis of the major human uracil-DNA glycosylase.

Authors:  G Slupphaug; L C Olsen; D Helland; R Aasland; H E Krokan
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

10.  Mismatch repair polymorphisms and risk of colon cancer, tumour microsatellite instability and interactions with lifestyle factors.

Authors:  P T Campbell; K Curtin; C M Ulrich; W S Samowitz; J Bigler; C M Velicer; B Caan; J D Potter; M L Slattery
Journal:  Gut       Date:  2008-06-03       Impact factor: 23.059

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