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首页> 外文期刊>Pathology oncology research: POR >The Value of a Novel Panel of Cervical Cancer Biomarkers for Triage of HPV Positive Patients and for Detecting Disease Progression
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The Value of a Novel Panel of Cervical Cancer Biomarkers for Triage of HPV Positive Patients and for Detecting Disease Progression

机译:新型宫颈癌生物标记物对HPV阳性患者的分类和疾病进展检测的价值

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id="Par1" class="Para">In the era of primary vaccination against HPV and at the beginning of the low prevalence of cervical lesions, introduction of screening methods that can distinguish between low- and high-grade lesions is necessary in order to maintain the positive predictive value of screening. This case-control study included 562 women who attended cervical screening or were referred for colposcopy and 140 disease free controls, confirmed by histology and/or cytology. The cases were stratified by age. Using routine exfoliated liquid based cytological samples RT-PCR measurements of biomarker genes, high-risk HPV testing and liquid based cytology were performed and used to evaluate different testing protocols including sets of genes/tests with different test cut-offs for the diagnostic panels. Three new panels of cellular biomarkers for improved triage of hrHPV positive women (diagnostic panel) and for prognostic assessment of CIN lesions were proposed. The diagnostic panel (PIK3AP1, TP63 and DSG3) has the potential to distinguish cytologically normal hrHPV+ women from hrHPV+ women with CIN2+. The prognostic gene panels (KRT78, MUC5AC, BPIFB1 and CXCL13, TP63, DSG3) have the ability to differentiate hrHPV+ CIN1 and carcinoma cases. The diagnostic triage panel showed good likelihood ratios for all age groups. The panel showed age-unrelated performance and even better diagnostic value under age 30, a unique feature among the established cervical triage tests. The prognostic gene-panels demonstrated good discriminatory power and oncogenic, anti-oncogenic grouping of genes. The study highlights the potential for the gene expression panels to be used for diagnostic triage and lesion prognostics in cervical cancer screening.
机译:id =“ Par1” class =“ Para”>在针对HPV的初次疫苗接种时代以及子宫颈病变的低流行初期,有必要引入能够区分低度和高度病变的筛查方法为了保持筛查的积极预测价值。这项病例对照研究包括562名接受宫颈癌筛查或接受阴道镜检查的妇女以及140名无病对照,这些均通过组织学和/或细胞学检查证实。病例按年龄分层。使用常规剥落的基于液体的细胞学样本对生物标志物基因进行RT-PCR测量,进行高风险的HPV检测和基于液体的细胞学检查,并用于评估不同的检测方案,包括用于诊断面板的具有不同检测截止值的基因/检测集。提出了三个新的细胞生物标记物组,用于改善hrHPV阳性女性的分类(诊断组)和用于CIN病变的预后评估。诊断小组(PIK3AP1,TP63和DSG3)有可能将细胞学上正常的hrHPV +妇女与具有CIN2 +的hrHPV +妇女区分开。预后基因组(KRT78,MUC5AC,BPIFB1和CXCL13,TP63,DSG3)具有区分hrHPV + CIN1和癌症病例的能力。诊断分类分类小组显示了所有年龄组的良好似然比。专家组显示了与年龄无关的性能,甚至在30岁以下具有更好的诊断价值,这是既定的宫颈分诊测试中的独特功能。预后基因面板显示出良好的区分力和基因的致癌,抗癌分组。该研究强调了基因表达面板在宫颈癌筛查中用于诊断分类和病变预后的潜力。

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