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Formation of N-7-(2-carbamoyl-2-hydroxyethyl)guanine in DNA of the mouse and the rat following intraperitoneal administration of [14C]acrylamide

Segerbäck, Dan, Calleman, Carl Johan, Schroeder, Jesara L., Costa, Lucio G., Faustman, Elaine M.·1995·Carcinogenesis

Abstract

Acrylamide is an alkylating agent which reacts very slowly in direct reactions with DNA and is negative in the Ames test, but is carcinogenic in mice and rats. In order to explain the cancer-initiating properties of acrylamide we have studied DNA adduct formation in vitro with a metabolizing system and in vivo in mice and rats following i.p. administration of 14C-labeled acrylamide. A major adduct found in both species was N-7-(2-carbamoyl-2-hydroxy-ethyl)guanine, formed by reaction of the DNA with the epoxide metabolite glycidamide. The levels of this adduct were similar in the different organs of the two rodent species, which supports the notion that glycidamide is relatively evenly distributed among tissues and that the organ-specificity in acrylamide carcinogenesis cannot be explained by a selective accumulation of the DNA-reactive metabolite in target organs.

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Metadata

Authors
Segerbäck, D., Calleman, C. J., Schroeder, J. L., Costa, L. G., & Faustman, E. M.
Venue
Carcinogenesis
Published
1995
Volume
16
Issue
5
Pages
1161-1165
ISSN
  • 0143-3334 (ISSN-L)
  • 1460-2180
OpenAlex
W2005740946
Cited by
230
References
0
FWCI
0.64
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Formation of N-7-(2-carbamoyl-2-hydroxyethyl)guanine in DNA of the mouse and the rat following intraperitoneal administration of [14C]acrylamide. https://app.cochat.ai/papers/10.1093/carcin/16.5.1161
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Segerbäck, D., Calleman, C. J., Schroeder, J. L., Costa, L. G., & Faustman, E. M. (1995). Formation of N-7-(2-carbamoyl-2-hydroxyethyl)guanine in DNA of the mouse and the rat following intraperitoneal administration of [14C]acrylamide. Carcinogenesis. https://doi.org/10.1093/carcin/16.5.1161

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