首页> 美国卫生研究院文献>American Journal of Cancer Research >TMEM45A SERPINB5 and p16INK4A transcript levels are predictive for development of high-grade cervical lesions
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TMEM45A SERPINB5 and p16INK4A transcript levels are predictive for development of high-grade cervical lesions

机译:TMEM45ASERPINB5和p16INK4A转录水平可预测高度宫颈病变的发展

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摘要

Women persistently infected with human papillomavirus (HPV) type 16 are at high risk for development of cervical intraepithelial neoplasia grade 3 or cervical cancer (CIN3+). We aimed to identify biomarkers for progression to CIN3+ in women with persistent HPV16 infection. In this prospective study, 11,088 women aged 20-29 years were enrolled during 1991-1993, and re-invited for a second visit two years later. Cervical cytology samples obtained at both visits were tested for HPV DNA by Hybrid Capture 2 (HC2), and HC2-positive samples were genotyped by INNO-LiPA. The cohort was followed for up to 19 years via a national pathology register. To identify markers for progression to CIN3+, we performed microarray analysis on RNA extracted from cervical swabs of 30 women with persistent HPV16-infection and 11 HPV-negative women. Six genes were selected and validated by quantitative PCR. Three genes were subsequently validated within a different and large group of women from the same cohort. Secondly, Kaplan-Meier and Cox-regression analyses were used to investigate whether expression levels of those three genes predict progression to CIN3+. We found that high transcript levels of TMEM45A, SERPINB5 and p16INK4a at baseline were associated with increased risk of CIN3+ during follow-up. The hazard ratios of CIN3+ per 10-fold increase in baseline expression level were 1.6 (95% CI: 1.1-2.3) for TMEM45A, 1.6 (95% CI: 1.1-2.5) for p16INK4a, and 1.8 (95% CI: 1.2-2.7) for SERPINB5. In conclusion, high mRNA expression levels of TMEM45A, SERPINB5 and p16INK4a were associated with increased risk of CIN3+ in persistently HPV16-infected women.
机译:持续感染16型人类乳头瘤病毒(HPV)的妇女极有可能发展为3级宫颈上皮内瘤变或宫颈癌(CIN3 +)。我们的目的是鉴定持续性HPV16感染女性进展为CIN3 +的生物标志物。在这项前瞻性研究中,1991-1993年招募了11088名20-29岁的女性,并在两年后再次邀请其第二次访问。通过Hybrid Capture 2(HC2)测试了两次访视时获得的宫颈细胞学样本的HPV DNA,并通过INNO-LiPA对HC2阳性样本进行了基因分型。该队列通过国家病理学记录进行了长达19年的随访。为了鉴定进展为CIN3 +的标志物,我们对从30例持续感染HPV16的女性和11例HPV阴性的女性的宫颈拭子中提取的RNA进行了微阵列分析。选择了六个基因,并通过定量PCR进行了验证。随后,在同一队列的一组不同的大批女性中验证了三个基因。其次,使用Kaplan-Meier和Cox回归分析来研究这三个基因的表达水平是否预测向CIN3 +的进展。我们发现基线时TMEM45A,SERPINB5和p16INK4a的高转录水平与随访期间CIN3 +的风险增加有关。基线表达水平每升高10倍CIN3 +的危险比对于TMEM45A为1.6(95%CI:1.1-2.5),对于p16INK4a为1.6(95%CI:1.1-2.5)和1.8(95%CI:1.2-) 2.7)用于SERPINB5。总之,在持续感染HPV16的女性中,TMEM45A,SERPINB5和p16INK4a的高mRNA表达水平与CIN3 +风险增加有关。

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