Literature DB >> 12605383

Mutations induced by (-)-anti-11R,12S-dihydrodiol 13S,14R-epoxide of dibenzo[a,l]pyrene in the coding region of the hypoxanthine phosphoribosyltransferase (Hprt) gene in Chinese hamster V79 cells.

Brinda Mahadevan1, Wan-Mohaiza Dashwood, Andreas Luch, Arta Pecaj, Johannes Doehmer, Albrecht Seidel, Cliff Pereira, William M Baird.   

Abstract

The polycyclic aromatic hydrocarbon dibenzo[a,l]pyrene (DB[a,l]P) is an exceptionally potent carcinogen. Its direct DNA-reactive metabolite, the fjord region (-)-anti-11R,12S-dihydrodiol 13S,14R-epoxide [(-)-anti-DB[a,l]PDE], was used to investigate induction of mutations in the coding region of the hypoxanthine phosphoribosyltransferase (Hprt) gene in Chinese hamster V79 cells. Cells exposed to 1-10 nM (-)-anti-DB[a,l]PDE exhibited a close dose-responsive increase in the frequency of mutant clones resistant to 6-thioguanine. RNA was isolated from mutant clones and cDNAs were prepared by reverse transcription. The coding region of the cDNA of the Hprt gene was amplified by polymerase chain reaction and sequenced. Analysis of the DNA base sequence changes induced by (-)-anti-DB[a,l]PDE indicated that base substitutions were the most prevalent mutations, followed by exon deletions. Among the groups of V79 cells treated with low concentrations of (-)-anti-DB[a,l]PDE, most displayed high selectivity for both A:T-->T:A transversions and A:T-->G:C transitions, while cells exposed to a higher dose (10 nM) formed predominantly G:C-->T:A transversions. Also, the number of base substitutions per mutant clone increased with dose. In general, the mutation profiles induced by (-)-anti-DB[a,l]PDE exhibited a wide spectrum; in addition to base substitutions, deletions, insertions, frameshift mutations, as well as tandem mutations were detected. Analysis of the DNA adduct levels induced by (-)-anti-DB[a,l]PDE revealed that a concentration-dependent increase in the level of adduct formation preceded the concentration-dependent increase in mutational events in these cells and that an increasing proportion of DNA adducts at deoxyadenosine were formed with dose. The results of this study demonstrate a correspondence between the concentration and types of DNA adducts and the frequency and types of mutations induced by (-)-anti-DB[a,l]PDE in V79 cells. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12605383     DOI: 10.1002/em.10136

Source DB:  PubMed          Journal:  Environ Mol Mutagen        ISSN: 0893-6692            Impact factor:   3.216


  10 in total

1.  Human Microdosing with Carcinogenic Polycyclic Aromatic Hydrocarbons: In Vivo Pharmacokinetics of Dibenzo[def,p]chrysene and Metabolites by UPLC Accelerator Mass Spectrometry.

Authors:  Erin P Madeen; Ted J Ognibene; Richard A Corley; Tammie J McQuistan; Marilyn C Henderson; William M Baird; Graham Bench; Ken W Turteltaub; David E Williams
Journal:  Chem Res Toxicol       Date:  2016-09-09       Impact factor: 3.739

2.  Induction of ovarian cancer and DNA adducts by Dibenzo[a,l]pyrene in the mouse.

Authors:  Kun-Ming Chen; Shang-Min Zhang; Cesar Aliaga; Yuan-Wan Sun; Timothy Cooper; Krishnegowda Gowdahalli; Junjia Zhu; Shantu Amin; Karam El-Bayoumy
Journal:  Chem Res Toxicol       Date:  2012-01-06       Impact factor: 3.739

3.  Intercalative conformations of the 14R (+)- and 14S (-)-trans-anti-DB[a,l]P-N⁶-dA adducts: molecular modeling and MD simulations.

Authors:  Yuqin Cai; Shuang Ding; Nicholas E Geacintov; Suse Broyde
Journal:  Chem Res Toxicol       Date:  2011-02-28       Impact factor: 3.739

4.  Investigation of the genotoxicity of dibenzo[c,p]chrysene in human carcinoma MCF-7 cells in culture.

Authors:  Brinda Mahadevan; Andreas Luch; Jennifer Atkin; Tuan Nguyen; Arun K Sharma; Shantu Amin; William M Baird
Journal:  Chem Biol Interact       Date:  2006-11-13       Impact factor: 5.192

5.  Nuclear magnetic resonance solution structure of an N(2)-guanine DNA adduct derived from the potent tumorigen dibenzo[a,l]pyrene: intercalation from the minor groove with ruptured Watson-Crick base pairing.

Authors:  Yijin Tang; Zhi Liu; Shuang Ding; Chin H Lin; Yuqin Cai; Fabian A Rodriguez; Jane M Sayer; Donald M Jerina; Shantu Amin; Suse Broyde; Nicholas E Geacintov
Journal:  Biochemistry       Date:  2012-11-15       Impact factor: 3.162

6.  Adenine-DNA adducts derived from the highly tumorigenic Dibenzo[a,l]pyrene are resistant to nucleotide excision repair while guanine adducts are not.

Authors:  Konstantin Kropachev; Marina Kolbanovskiy; Zhi Liu; Yuqin Cai; Lu Zhang; Adam G Schwaid; Alexander Kolbanovskiy; Shuang Ding; Shantu Amin; Suse Broyde; Nicholas E Geacintov
Journal:  Chem Res Toxicol       Date:  2013-04-24       Impact factor: 3.739

7.  The role of polycyclic aromatic hydrocarbon-DNA adducts in inducing mutations in mouse skin.

Authors:  Dhrubajyoti Chakravarti; Divya Venugopal; Paula C Mailander; Jane L Meza; Sheila Higginbotham; Ercole L Cavalieri; Eleanor G Rogan
Journal:  Mutat Res       Date:  2007-09-07       Impact factor: 2.433

8.  Human in Vivo Pharmacokinetics of [(14)C]Dibenzo[def,p]chrysene by Accelerator Mass Spectrometry Following Oral Microdosing.

Authors:  Erin Madeen; Richard A Corley; Susan Crowell; Kenneth Turteltaub; Ted Ognibene; Mike Malfatti; Tammie J McQuistan; Mary Garrard; Dan Sudakin; David E Williams
Journal:  Chem Res Toxicol       Date:  2014-12-10       Impact factor: 3.739

Review 9.  Repair-Resistant DNA Lesions.

Authors:  Nicholas E Geacintov; Suse Broyde
Journal:  Chem Res Toxicol       Date:  2017-08-10       Impact factor: 3.739

10.  Data in support of the mutagenic potential of the isoflavone irilone in cultured V79 cells.

Authors:  Anne Scheffler; Annette E Albrecht; Harald L Esch; Leane Lehmann
Journal:  Data Brief       Date:  2015-07-17
  10 in total

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