期刊
JOURNAL OF INFECTIOUS DISEASES
卷 199, 期 1, 页码 20-30出版社
OXFORD UNIV PRESS INC
DOI: 10.1086/595563
关键词
-
资金
- DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS [N01CP021081] Funding Source: NIH RePORTER
- NATIONAL CANCER INSTITUTE [U01CA078527, R01CA078527, ZIACP010124, ZIACP010206] Funding Source: NIH RePORTER
- Intramural NIH HHS Funding Source: Medline
- NCI NIH HHS [CA-78527, U01 CA078527, CP-31061, CP-21081, CO-12400, N01CO12400, R01 CA078527] Funding Source: Medline
Background. We examined host genetic factors to identify those more common in individuals whose human papillomavirus (HPV) infections were most likely to persist and progress to cervical intraepithelial neoplasia grade 3 (CIN3) and cancer. Methods. We genotyped 92 single-nucleotide polymorphisms (SNPs) from 49 candidate immune response and DNA repair genes obtained from 469 women with CIN3 or cancer, 390 women with persistent HPV infections (median duration, 25 months), and 452 random control subjects from the 10,049-woman Guanacaste Costa Rica Natural History Study. We calculated odds ratios and 95% confidence intervals (CIs) for the association of SNP and haplotypes in women with CIN3 or cancer and HPV persistence, compared with random control subjects. Results. A SNP in the Fanconi anemia complementation group A gene (FANCA) (G501S) was associated with increased risk of CIN3 or cancer. The AG and GG genotypes had a 1.3-fold (95% CI, 0.95-1.8-fold) and 1.7-fold ( 95% CI, 1.1-2.6-fold) increased risk for CIN3 or cancer, respectively (P-trend =.008; referent, AA). The FANCA haplotype that included G501S also conferred increased risk of CIN3 or cancer, as did a different haplotype that included 2 other FANCA SNPs (G809A and T266A). A SNP in the innate immune gene IRF3 (S427T) was associated with increased risk for HPV persistence (P-trend =.009). Conclusions. Our results require replication but support the role of FANCA variants in cervical cancer susceptibility and of IRF3 in HPV persistence.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据