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首页> 外文期刊>Human Immunology: Official Journal of the American Society for Histocompatibility and Immunogenetics >MICA and KLRK1 genes and their impact in cervical intraepithelial neoplasia development in the southern Brazilian population
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MICA and KLRK1 genes and their impact in cervical intraepithelial neoplasia development in the southern Brazilian population

机译:云母和KLRK1基因及其对巴西南部宫颈上皮内瘤形成发展的影响

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摘要

Cervical carcinoma and cervical intraepithelial neoplasia (CIN) are associated with persistent infection by oncogenic subtypes of HPV (Human Papillomavirus). Factors linked to immunity, genetics and others like oral contraceptive use, sexual behavior, coinfections with other microorganisms and smoking seem to influence the mechanisms that determine regression or progression to CIN and cervical cancer. We investigated the effect of the MHC class I chain-related gene A (MICA) and Killer Cell Lectin Like receptor K1 (KLRK1) genes on cervical cancer and CIN lesions susceptibility in a group of 195 patients from southern Brazil. There were found a significantly higher number of ex-smokers in the control group (p = 0.005). There were more oral contraceptives (OC) users in the patient group. MICA*008:01/04 allele showed a significant difference between patient and control groups (p = 0.03; OR = 0.63, 95% CI 0.41-0.96), as well as MICA*018:01(p = 0.004, OR = 0.15, 95% CI 0.03-0.64) and MICA*002:01/020 (p = 0.01; OR = 0.60, 95% CI 0.40-0.88). We also analyzed cases and controls according to the MICA-129 genotypes (Met/Val). There was found a difference (p = 0.02) with the Met/Val genotype in a higher frequency in controls and Val/Val and Val/MICA del at a higher frequency in the patient group. For the KLRK1 gene there was no significant difference between groups.
机译:宫颈癌和宫颈上皮内瘤周期(CIN)与HPV(人乳头瘤病毒)的致癌亚型持续感染有关。与免疫力相关的因素,遗传学和其他像口服避孕药,性行为,与其他微生物和吸烟的繁殖似乎会影响确定对CIN和宫颈癌的回归或进展的机制。我们研究了MHC类I链相关基因A(MICA)和杀手细胞凝集素在巴西南部的195名患者中对宫颈癌和CIN病变易感性的影响。在对照组中发现了较高的出吸烟者(P = 0.005)。患者组中有更多口服避孕药(OC)用户。 MICA * 008:01/04等位基因显示患者和对照组之间存在显着差异(P = 0.03;或= 0.63,95%CI 0.41-0.96),以及云母* 018:01(p = 0.004,或= 0.15 ,95%CI 0.03-0.64)和云母* 002:01/020(P = 0.01;或= 0.60,95%CI 0.40-0.88)。我们还根据MICA-129基因型(MET / VAL)分析病例和对照。在患者组中,在对照组和Val / val和val / Mica Del中的较高频率下,在较高频率下发现了差异(p = 0.02)。对于KLRK1基因,组之间没有显着差异。

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