| GeneLibs

题目:: Genetic variant of CCND1: association with HPV-mediated cervical cancer in Indian population.
作者:: Thakur(Nisha),Hussain(Showket),Kohaar(Indu),Tabassum(Rubina),Nasare(Vilas),Tiwari(Pratibha),Batra(Swaraj),Bhambhani(Suresh),Das(Bhudev C),Basir(Seemi Farhat),Bharadwaj(Dwaipayan),Bharadwaj(Mausumi)
状态:: 发布时间2009-06-03 , 更新时间 2009-06-03
期刊:: Biomarkers
摘要:: The potential association of single nucleotide polymorphisms (SNPs) (G870A and G1722C) of CCND1 with susceptibility to cervical cancer was investigated. The study included 200 cervical cancer cases along with an equal number of healthy controls. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis and direct sequencing were employed for genotyping. We found that women carrying the 870AA genotype have a 2.49-fold increased risk for the development of cervical cancer (odds ratio (OR) 2.49; 95% confidence interval (CI) 1.51-4.09; p = 0.0004) compared with GG+GA genotypes. For the 1722 locus, the frequency of the polymorphic 'C' allele was strongly associated with a reduced risk of cervical cancer (p = 0.019; OR 0.71; 95% CI 0.54-0.94). Our data suggest that CCND1 G870A polymorphism could act as a risk factor for the development of cervical cancer. And G1722C polymorphism may play a protective role against the development of human papillomavirus-associated cervical cancer among Indian women.
语言:: eng
DOI:: 10.1080/13547500902825274

文献库文献相关信息

DataTable pData

联系方式

微信公众号

文献库 文献相关信息

DataTable pData

联系方式

微信公众号

文献库文献相关信息