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HPV E6/E7和STAT3 mRNA检测在宫颈癌筛查中的临床价值

The clinical value of HPV E6/E7 and STAT3 mRNA detection in cervical cancer screening.

作者信息

Fan Yibing, Shen Zongji

机构信息

The First Affiliated Hospital of Soochow University, Suzhou 215006, China.

Department of Obstetrics and Gynecology, The Fifth Clinical Medical College of Yangzhou University, The Second People's Hospital of Changshu City, Suzhou 215006, China.

出版信息

Pathol Res Pract. 2018 May;214(5):767-775. doi: 10.1016/j.prp.2018.02.003. Epub 2018 Feb 11.

Abstract

OBJECTIVE

To explore the value of human papillomavirus (HPV) E6/E7 and signal transducer and activator of transcription 3 (STAT3) mRNA detection in the screening of cervical lesions.

METHODS

192 patients with abnormal ThinPrep cytology test (TCT) results and/or high-risk HPV infection were screened to identify possible cervical lesions in cases. Diagnoses were confirmed by histopathology. Fluorescence in situ hybridization (FISH) was performed to detect and qualify the mRNAs of HPV E6/E7, STAT3, and Survivin in cervical exfoliated cells. In addition, the performance of separate and combined mRNA detection methods were compared with TCT, HR-HPV DNA schemes respectively.

RESULTS

  1. Compared with HPVE6/E7 and STAT3 mRNA methods, Survivin mRNA assay had poor specificity (Sp), Youden index (YI) and concordance rate. 2. HPV E6/E7, STAT3, and STAT3 + HR-HPV methods had the best Sp, concordance rate and positive predictive value (PPV) for cervical lesions screening and atypical squamous cells of undetermined significance (ASCUS) triage. For screening of high grade squamous intraepithelial lesions or greater (HSILs+), no difference was observed in the Se of mRNA detection methods in comparison with that of TCT, HR-HPV and TCT + HR-HPV, whereas the false positive rate (FPR) decreased by 41.48%/55.99%/17.19% and the colposcopy referral rate reduced by about 20.00%/25.00%/11.17%. For triage of women with ASCUS, no difference was observed in the Se of mRNA detection methods as compared to that of HR-HPV (χ = 1.05, P > 0.75), while the FPR decreased by 45.83%/37.50%/41.66% and the colposcopy referral rate reduced by 32.42%/22.60%/25.28%, respectively. The Se, YI, and PPV of the combined methods increased in comparison to each method alone. 3. Compared with the TCT + HR-HPV method, HPV E6/E7 + STAT3 method had perfect Sp (95.92%) and PPV (95.40%) for screening HSILs+, the FPR and colposcopy referral rate decreased by 31.06% and 22.48% respectively.

CONCLUSIONS

  1. The expression of HPV E6/E7 and STAT3 mRNA confirmed using FISH assay is expected to be a new method and molecular marker for cervical lesions screening. Survivin mRNA was excluded due to its poor performance. 2. HPV E6/E7, STAT3, and STAT3 +HR-HPV assays could be new approaches for cervical cancer screening and ASCUS triage, and the efficiency of combined screening program was better than that of a separate one. 3. HPV E6/E7 + STAT3 regimen is expected to be a diagnostic strategy for cervical lesions.
摘要

目的

探讨人乳头瘤病毒(HPV)E6/E7及信号转导与转录激活因子3(STAT3)mRNA检测在宫颈病变筛查中的价值。

方法

对192例液基薄层细胞学检测(TCT)结果异常和/或高危型HPV感染患者进行筛查,以确定可能存在的宫颈病变情况。诊断经组织病理学确诊。采用荧光原位杂交(FISH)技术检测宫颈脱落细胞中HPV E6/E7、STAT3和生存素(Survivin)的mRNA,并对其进行定量分析。此外,分别将单独及联合mRNA检测方法的性能与TCT、高危型HPV DNA检测方案进行比较。

结果

  1. 与HPV E6/E7和STAT3 mRNA检测方法相比,Survivin mRNA检测的特异性(Sp)、约登指数(YI)及符合率较差。2. HPV E6/E7、STAT3及STAT3 +高危型HPV检测方法在宫颈病变筛查及意义不明确的非典型鳞状细胞(ASCUS)分流方面具有最佳的Sp、符合率及阳性预测值(PPV)。对于高级别鳞状上皮内病变或更高级别病变(HSILs+)的筛查,mRNA检测方法与TCT、高危型HPV及TCT +高危型HPV检测方法相比,敏感性(Se)无差异,而假阳性率(FPR)分别降低了41.48%/55.99%/17.19%,阴道镜转诊率降低了约20.00%/25.00%/11.17%。对于ASCUS患者的分流,mRNA检测方法与高危型HPV检测方法相比,Se无差异(χ = 1.05,P > 0.75),而FPR分别降低了45.83%/37.50%/41.66%,阴道镜转诊率分别降低了32.42%/22.60%/25.28%。联合检测方法的Se、YI及PPV较各单独检测方法均有所提高。3. 与TCT +高危型HPV检测方法相比,HPV E6/E7 + STAT3检测方法对HSILs+筛查具有理想的Sp(95.92%)和PPV(95.40%),FPR和阴道镜转诊率分别降低了31.06%和22.48%。

结论

  1. 采用FISH技术证实的HPV E6/E7和STAT3 mRNA表达有望成为宫颈病变筛查的新方法及分子标志物。Survivin mRNA因性能较差被排除。2. HPV E6/E7、STAT3及STAT3 +高危型HPV检测可作为宫颈癌筛查及ASCUS分流的新方法,联合筛查方案的效率优于单独检测。3. HPV E6/E7 + STAT3检测方案有望成为宫颈病变的诊断策略。

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