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ERCC1 Polymorphisms and Risk of Adult Glioma in a Chinese Population: A Hospital-Based Case-Control Study
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Citations
20
References
2011
Year
GeneticsGenetic EpidemiologyImmunologyPathologyHuman PolymorphismDisease Gene IdentificationImmune-related Gene PolymorphismGliomaClinical GeneticsNeuro-oncologyOncologyNeurologyAdult GliomaCancer ResearchVariant InterpretationCancer GeneticsErcc1 GeneCancer RiskMedicineErcc1 PolymorphismsChinese Population
To examine the associations of two polymorphisms in excision repair cross-complementing rodent repair deficiency complementation group 1 (ERCC1) gene, C8092A (rs3212986) and T19007C (rs11615), with the risk of adult glioma, we performed a hospital-based case-control study with 257 new cases of glioma and 278 controls in Wenzhou, China. Results showed that polymorphisms C8092A and T19007C in ERCC1 gene were not associated with the risk of glioma in a Chinese population. Further studies in Chinese populations with larger sample sizes are still warranted.
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