Literature DB >> 11043496

Development of a 32P-postlabelling method for the detection of 1,N2-propanodeoxyguanosine adducts of crotonaldehyde in vivo.

B D Schuler1, E Eder.   

Abstract

Crotonaldehyde is a genotoxic, mutagenic and carcinogenic alpha,beta-unsaturated carbonyl compound which forms 1,N2-propanodeoxyguanosine adducts. Humans are exposed to this compound at work places, and from tobacco smoke and air pollution, but also from food and beverages. Therefore crotonaldehyde can play a significant role in carcinogenesis. Since in vivo measurement of DNA adducts of crotonaldehyde can improve cancer risk assessment and contribute to the clarification of the role of crotonaldehyde in carcinogenicity, we developed, adapted and optimized a 32P-postlabelling technique for the adducts of crotonaldehyde based on nuclease P1 enrichment and on a polyethylene imine modified cellulose TLC to provide a detection sensitivity of three adducts per 10(9) nucleotides and a labelling efficiency of 80-90%. We also report a readily performable synthesis of adduct standards and demonstrated that DNA is completely digested to the 3'-monophosphate nucleotides under the conditions of our enzymatic DNA hydrolysis. We showed that the postlabelling method developed is appropriate for in vivo DNA-binding studies. Female Fischer 344 rats were treated by gavage with crotonaldehyde at doses of 200 and 300 mg/kg body weight, and 20 h after treatment adduct levels of 2.9 and 3.4 adducts per 10(8) nucleotides, respectively, were found in the liver DNA. Only 1.6 nucleotides per 10(8) nucleotides were found 12 h after treatment at 200 mg/kg body weight. Absolutely no adducts could be found in liver DNA of untreated rats with our method at the detection limit of three adducts per 10(9) nucleotides. In contrast to our group, the group of Chung have reported crotonaldehyde adduct levels in the range of 2.2 22 adducts per 10(8) nucleotides in DNA of untreated Fischer 344 rats. The clarification of this discrepancy is of importance for the elucidation of the role of crotonaldehyde in carcinogenicity, and both groups have decided to clarify this in cooperation in the near future.

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Year:  2000        PMID: 11043496     DOI: 10.1007/s002040000142

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  5 in total

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Journal:  Biochem Biophys Res Commun       Date:  2009-06-27       Impact factor: 3.575

2.  AKR1B10 activates diacylglycerol (DAG) second messenger in breast cancer cells.

Authors:  Chenfei Huang; Zhe Cao; Jun Ma; Yi Shen; Yiwen Bu; Ramina Khoshaba; Guiyuan Shi; Dan Huang; Duan-Fang Liao; Haitao Ji; Junfei Jin; Deliang Cao
Journal:  Mol Carcinog       Date:  2018-06-28       Impact factor: 4.784

3.  Analysis of crotonaldehyde- and acetaldehyde-derived 1,n(2)-propanodeoxyguanosine adducts in DNA from human tissues using liquid chromatography electrospray ionization tandem mass spectrometry.

Authors:  Siyi Zhang; Peter W Villalta; Mingyao Wang; Stephen S Hecht
Journal:  Chem Res Toxicol       Date:  2006-10       Impact factor: 3.739

4.  Human aldo-keto reductases 1B1 and 1B10: a comparative study on their enzyme activity toward electrophilic carbonyl compounds.

Authors:  Yi Shen; Linlin Zhong; Stephen Johnson; Deliang Cao
Journal:  Chem Biol Interact       Date:  2011-02-15       Impact factor: 5.192

Review 5.  Oxidative Stress and Carbonyl Lesions in Ulcerative Colitis and Associated Colorectal Cancer.

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Journal:  Oxid Med Cell Longev       Date:  2015-12-28       Impact factor: 6.543

  5 in total

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