2009
DOI: 10.1016/j.lungcan.2008.12.009
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A meta-analysis of TP53 codon 72 polymorphism and lung cancer risk: Evidence from 15,857 subjects

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Cited by 29 publications
(16 citation statements)
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“…The allele frequencies of p53 Pro and MDM2 G were 0.485 and 0.419, respectively, among healthy control subjects in this study; these values are similar to those of other studies on Chinese populations (0.38-0.52 and 0.42-0.52, respectively) (Hu et al, 2006;Zhang et al, 2006;Chua et al, 2010;Liu et al, 2013). Li et al (Li et al, 2009) reported the OR for Asians carrying Pro/Pro genotype to be 1.395 (95% CI = 1.206-1.613), which is much higher than that of Caucasians. Zhang et al (2006) found that smoking modified the association between the p53 Arg72Pro polymorphism and lung cancer; in contrast, both Piao et al (2011) andSakiyama et al (2005) found that it did not.…”
Section: Discussionsupporting
confidence: 90%
“…The allele frequencies of p53 Pro and MDM2 G were 0.485 and 0.419, respectively, among healthy control subjects in this study; these values are similar to those of other studies on Chinese populations (0.38-0.52 and 0.42-0.52, respectively) (Hu et al, 2006;Zhang et al, 2006;Chua et al, 2010;Liu et al, 2013). Li et al (Li et al, 2009) reported the OR for Asians carrying Pro/Pro genotype to be 1.395 (95% CI = 1.206-1.613), which is much higher than that of Caucasians. Zhang et al (2006) found that smoking modified the association between the p53 Arg72Pro polymorphism and lung cancer; in contrast, both Piao et al (2011) andSakiyama et al (2005) found that it did not.…”
Section: Discussionsupporting
confidence: 90%
“…Interestingly, an age-associated change in the TP53 genotype distribution was also observed for lung cancer: the elderly (60-79 yr) affected subjects were characterized by an increased frequency of TP53 major genotypes, whereas a high proportion of heterozygous genotype combinations was frequently detected in mature (40-59 yr) patients Gervas et al, 2007). These data not only agreed with recent meta-analyses (Dai et al, 2009;Francisco et al, 2010;Li et al, 2009;Yan et al, 2009) but also suggest that age might be an important modifier of the association between TP53 rs1042522 polymorphism and lung cancer risk. With regard to rs17878362 and rs1625895 germline variations, the alteration in frequency of their genotypes is most likely linked to the regulation of TP53 gene dosage particularly that which results in an increase in expression of the rs1042522 G allele, as already mentioned previously.…”
Section: Tp53 Polymorphismssupporting
confidence: 90%
“…However, in spite of the present disagreements and methodological flaws, association tendencies for some cancer localizations are clear (Table 2). Simply stated, the rs1042522 C allele is associated with increased susceptibility to cancers, including of the lung (Dai et al, 2009;Francisco et al, 2010;Li et al, 2009;Yan et al, 2009), head and neck (Francisco et al, 2010), thyroid (Francisco et al, 2010), esophagus Zhao et al, 2010), pancreas , liver Francisco et al, 2010), gallbladder , nasopharynx (Zhuo et al, 2009b), and cervix (Francisco et al, 2010;Klug et al, 2009). No significant contribution of TP53 rs1042522 polymorphism to oral cancer has been reported (Zhuo et al, 2009c).…”
Section: Tp53 Polymorphisms: the Cancer Predisposing Valuementioning
confidence: 99%
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“…Finally, gene-gene and gene-environment interactions were not fully addressed in our meta-analysis owing to lack of sufficient data. Previous studies have demonstrated that interactions among smoking and some genetic polymorphisms were associated with lung cancer risk (Herbst et al, 2008;Li et al, 2009). Further studies are expected to explore potential gene-gene and gene-environment interactions.…”
Section: A B Discussionmentioning
confidence: 96%