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Erschienen in: Tumor Biology 6/2012

01.12.2012 | Research Article

CYP1A1 Ile462Val polymorphism and cervical cancer: evidence from a meta-analysis

verfasst von: Shuyan Yang, Changru Jia, Hong Zhu, Shiyu Han

Erschienen in: Tumor Biology | Ausgabe 6/2012

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Abstract

Many publications have evaluated the correlation between Cytochrome P450 1A1 (CYP1A1) Ile462Val polymorphism and cervical cancer risk, but the results remain inconclusive. To provide a more robust estimate of this effect, a meta-analysis was carried out. We systematically searched PubMed, Embase and CBM databases for studies published before May 2012. The association between CYP1A1 Ile462Val polymorphism and cervical cancer risk was assessed by calculating pooled odds ratios (OR) with its 95 % confidence intervals (95 % CI). On the basis of our inclusion criteria, ten studies with a total of 2,423 individuals were included in the meta-analysis. Overall, CYP1A1 Ile462Val polymorphism was associated with increased risk of cervical cancer (Val versus Ile, OR = 1.43; 95 % CI, 1.03–1.97; ValVal versus IleIle, OR = 2.43; 95 % CI, 1.19–4.95; ValVal+ValIle versus IleIle, OR = 1.59; 95 % CI, 1.00–2.53). Ethnic subgroup analyses showed a significant association was found in Caucasians (Val versus Ile, OR = 2.03; 95 % CI, 1.17–3.51; ValVal versus IleIle, OR = 2.74; 95 % CI, 1.30–5.75; ValVal+ValIle versus IleIle, OR = 2.50; 95 % CI, 1.33–4.70), but not in Asians. In conclusion, this meta-analysis suggests that CYP1A1 Ile462Val polymorphism plays an important role in susceptibility to cervical cancer. Further studies with large sample size and careful design need performing to identify this association more comprehensively.
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Metadaten
Titel
CYP1A1 Ile462Val polymorphism and cervical cancer: evidence from a meta-analysis
verfasst von
Shuyan Yang
Changru Jia
Hong Zhu
Shiyu Han
Publikationsdatum
01.12.2012
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 6/2012
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-012-0488-y

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