Source:http://linkedlifedata.com/resource/pubmed/id/20590474
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2010-10-26
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pubmed:abstractText |
DNA repair gene alterations may cause a reduction in DNA repair capacity and influence an individual's susceptibility to carcinogenesis. We hypothesized that single nucleotide polymorphisms of DNA repair genes may be a risk factor for prostate cancer (PCa) susceptibility, influencing expression of homologous recombination (XRCC3) and nonhomologous end-joining (XRCC7) genes and conferring predisposition to PCa. In a case-control study, genotyping was done in 192 patients with PCa and 224 age matched unrelated healthy controls of similar ethnicity to determine variants in XRCC3 Exon 7 (C18067T, rs861539), IVS5-14 (A17893G, rs1799796), and XRCC7 Intron 8 (G6721T, rs7003908) by polymerase chain reaction-restriction fragment-length polymorphism methods. Variant genotype GG (odds ratio [OR], 2.23; p=0.003) and combined genotype TG+GG (OR, 1.541; p=0.049), G allele of XRCC7 Intron 8 (G>T), demonstrated significant risk for PCa (OR, 1.529; p=0.002). Stratification on bases of Gleason grade and bone metastasis, significant risk with high Gleason grade for CT genotype of XRCC3 Exon 7, and variant genotype GG of XRCC7 Intron 8 were observed. Our results strongly support that common sequence variants (GG) genotype of XRCC7 may increase risk of PCa. G allele being a risk allele in our study also suggests that this polymorphism be used as a marker for the PCa susceptibility.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Activated Protein Kinase,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PRKDC protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/X-ray repair cross complementing...
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1557-7430
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
669-74
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pubmed:meshHeading |
pubmed-meshheading:20590474-Asian Continental Ancestry Group,
pubmed-meshheading:20590474-Bone Neoplasms,
pubmed-meshheading:20590474-Case-Control Studies,
pubmed-meshheading:20590474-Cohort Studies,
pubmed-meshheading:20590474-DNA Repair,
pubmed-meshheading:20590474-DNA-Activated Protein Kinase,
pubmed-meshheading:20590474-DNA-Binding Proteins,
pubmed-meshheading:20590474-Genetic Predisposition to Disease,
pubmed-meshheading:20590474-Genotype,
pubmed-meshheading:20590474-Humans,
pubmed-meshheading:20590474-India,
pubmed-meshheading:20590474-Male,
pubmed-meshheading:20590474-Middle Aged,
pubmed-meshheading:20590474-Nuclear Proteins,
pubmed-meshheading:20590474-Polymorphism, Single Nucleotide,
pubmed-meshheading:20590474-Prostatic Neoplasms,
pubmed-meshheading:20590474-Smoking
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pubmed:year |
2010
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pubmed:articleTitle |
Polymorphic variants of DNA repair gene XRCC3 and XRCC7 and risk of prostate cancer: a study from North Indian population.
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pubmed:affiliation |
Department of Urology and Renal Transplantation, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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