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Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes.

Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes. Research Abstract Details 

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  • Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes. Abstract Text:

    federica gemignaniFederica Gemignani,stefano landiStefano Landi,neonilia szeszenia-dabrowskaNeonilia Szeszenia-Dabrowska,david zaridzeDavid Zaridze,jolanta lissowskaJolanta Lissowska,peter rudnaiPeter Rudnai,eleonora fabianovaEleonora Fabianova,dana matesDana Mates,lenka foretovaLenka Foretova,vladimir janoutVladimir Janout,vladimir benckoVladimir Bencko, gaborieau Gaborieau,lydie gioia-patricolaLydie Gioia-Patricola,ilaria belliniIlaria Bellini,roberto baraleRoberto Barale,federico canzianFederico Canzian,janet hallJanet Hall,paolo boffettaPaolo Boffetta,rayjean j hungRayjean J Hung,paul brennanPaul Brennan,

    The role of genes coding for xenobiotic metabolizing enzymes (XMEs) and the risk of lung cancer is unclear. Under the assumption that these genes may be more important among people having a diagnosis of lung cancer at younger ages, we have investigated the role of single-nucleotide polymorphisms (SNPs) within phase I and phase II XME genes, and also genes involved in the metabolism of nucleic acids in a series of young onset patients and matched controls. We genotyped 299 lung cancer cases diagnosed before the age of 50 and 317 controls, from six countries of Central and Eastern Europe, by use of an oligonucleotide microarray and arrayed primer extension technique for 45 SNPs in 15 phase I XME genes, 46 SNPs in 17 phase II genes and 9 SNPs in 4 genes related to metabolism of nucleic acids. Heterozygote carriers of SNPs in CYP1A2 1545T>C, -164C>A and -740T>G; CYP2A6 -47A>C; MDR1 3435T>C; NAT1 1088T>A and 1095A>C; GSTA2 S112T; GSTM3 V224I and MTHFR A222V had altered risk of developing lung cancer. Phenotypes reconstructed after haplotype analyses showed that the carriers of the combined NAT1 fast+ NAT2 fast phenotypes were at lower risk when compared with those with the combined NAT1 slow + NAT2 slow acetylator phenotypes. Finally, extensive EPHX1 metabolizers showed an increased risk as compared with the poor metabolizers.

    Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes. Publishing Authors By Initials

    f gemignaniF Gemignani,s landiS Landi,n szeszenia-dabrowskaN Szeszenia-Dabrowska,d zaridzeD Zaridze,j lissowskaJ Lissowska,p rudnaiP Rudnai,e fabianovaE Fabianova,d matesD Mates,l foretovaL Foretova,v janoutV Janout,v benckoV Bencko,v gaborieauV Gaborieau,l gioia-patricolaL Gioia-Patricola,i belliniI Bellini,r baraleR Barale,f canzianF Canzian,j hallJ Hall,p boffettaP Boffetta,rj hungRJ Hung,p brennanP Brennan,

    For similar pharmaceutical preparations: xenobiotics research abstracts see: pharmaceutical preparations: xenobiotics research

    PUBMED ID PMID:

    MEDLINE DATE:

    Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Carcinogenesis

    VOLUME: 28

    Page Numbers: 1287-93

    Journal Abbreviation: Carcinogenesis

    ISSN: 0143-3334

    DAY: 27

    MONTH: 01

    YEAR: 2007

    Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8008055

    Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes. Keywords Mesh Terms:

    KEYWORDS: Xenobiotics

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes. Information

    Substance Name: Xenobiotics

    Registry Number: 0

    Grant and Affiliation Information for Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes.

    AFFILIATION: Genetics, Department of Biology, University of Pisa, Pisa, Italy.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NCI

    GRANT: R01 CA092039-01A2

    ACRONYM: CA

    MEDLINETA: Carcinogenesis

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    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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