Journal Article

The cytotoxicity of DNA carboxymethylation and methylation by the model carboxymethylating agent azaserine in human cells

M. O'Driscoll, P. Macpherson, Yao-Zhong Xu and P. Karran

in Carcinogenesis

Volume 20, issue 9, pages 1855-1862
Published in print September 1999 | ISSN: 0143-3334
Published online September 1999 | e-ISSN: 1460-2180 | DOI: http://dx.doi.org/10.1093/carcin/20.9.1855
The cytotoxicity of DNA carboxymethylation and methylation by the model carboxymethylating agent azaserine in human cells

More Like This

Show all results sharing this subject:

  • Clinical Cytogenetics and Molecular Genetics

GO

Show Summary Details

Preview

Carboxymethylating agents are potential sources of endogenous DNA damage that have been proposed as possible contributors to gastrointestinal carcinogenesis. The cytotoxicity of the model DNA carboxymethylating agent azaserine was investigated in human cells. Expression of the DNA repair enzyme O6-methylguanine-DNA methyltransferase (MGMT) did not affect sensitivity to the drug in two related Raji Burkitt's lymphoma cell lines. DNA mismatch repair-defective variants of Raji cells which display increased tolerance to DNA methylation damage were not selectively resistant to azaserine. Complementary results were obtained with a second carboxymethylating agent, potassium diazoacetate. In contrast, lymphoblastoid cell lines representative of each of the xeroderma pigmentosum complementation groups, including the variant, were all significantly more sensitive to azaserine than nucleotide excision repair-proficient cells. The hypersensitivity of XP cells was not due to systematic differences in the concentrations of intracellular thiol compounds or related thiol metabolizing enzymes. The data indicate that of the two types of potentially lethal DNA damage which azaserine introduces, carboxymethylated bases and O6-methylguanine, the former are repaired by nucleotide excision repair and are a more significant contributor to azaserine lethality in human cells.

Keywords: CDNB, 1-chloro-2,4-dinitrobenzene; CM, carboxymethyl; DON, 5′-diazo-6-oxonorleucine; GGT, γ-glutamyl transpeptidase; GSH, reduced glutathione; GST, glutathione S-transferase; HPRT, hypoxanthine-guanine phosphoribosyltransferase; KDA, potassium diazoacetate; MGMT, O6-methylguanine-DNA methyltransferase; MMR, mismatch repair; MNNG, N-methyl-N′-nitro-N-nitrosoguanidine; MNU, N-methyl-N-nitrosourea; N7-CMGua, N7-carboxymethylguanine; N3-CMAde, N3-carboxymethyladenine; NER, nucleotide excision repair; O6-CMGua, O6-carboxymethylguanine; O6-meGua, O6-methylguanine; S6-CMGua, S6-carboxymethylthioguanine; TG, 6-thioguanine; XP, xeroderma pigmentosum.

Journal Article.  5833 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.