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FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women

BACKGROUND: The current cervical cancer screening strategies based on Papanicolaou (Pap) and Human papillomavirus (HPV) tests receive great achievement but still exhibit many limitations in clinical practice. Exploring new biomarkers as stratified management method in HPV primary screening is becomi...

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Autores principales: Yang, Fan, Cui, Zifeng, Liao, Yuandong, Tian, Rui, Fan, Weiwen, Jin, Zhuang, Hu, Zheng, Yao, Shuzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175930/
https://www.ncbi.nlm.nih.gov/pubmed/31771040
http://dx.doi.org/10.3233/CBM-182232
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author Yang, Fan
Cui, Zifeng
Liao, Yuandong
Tian, Rui
Fan, Weiwen
Jin, Zhuang
Hu, Zheng
Yao, Shuzhong
author_facet Yang, Fan
Cui, Zifeng
Liao, Yuandong
Tian, Rui
Fan, Weiwen
Jin, Zhuang
Hu, Zheng
Yao, Shuzhong
author_sort Yang, Fan
collection PubMed
description BACKGROUND: The current cervical cancer screening strategies based on Papanicolaou (Pap) and Human papillomavirus (HPV) tests receive great achievement but still exhibit many limitations in clinical practice. Exploring new biomarkers as stratified management method in HPV primary screening is becoming the tendency of current research. METHODS: Immunocytochemistry (ICC) of FHIT and C-MYC were performed on exfoliated cervical cells from 197 eligible high-risk HPV positive women. Mann-Whitney U test, Pearson Chi-Square test, logistic regression analysis and receiver operating characteristic (ROC) curves were used to assess the diagnostic efficiency. RESULTS: ICC staining intensity of FHIT and C-MYC in high-grade cervical intraepithelial neoplasia (CIN) specimens was significantly different from low-grade CIN and normal specimens. Compared with Pap test, ROC analysis of ICC in detecting high-grade CIN resulted in a larger area under the curve (AUC) (0.805 and 0.814 vs 0.723, [Formula: see text] 0.001). FHIT achieved higher sensitivity than Pap test (79.41% vs 66.67%, [Formula: see text] 0.04). Logistic regression analysis of the combination of two biomarkers led to higher AUC value, specificity and PPV than any single biomarker. CONCLUSIONS: The utility of FHIT and C-MYC ICC analysis in cervical exfoliated cells of HPV-positive women displayed superior diagnostic potential and may improve clinical performance of cervical cancer screening.
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spelling pubmed-71759302020-04-28 FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women Yang, Fan Cui, Zifeng Liao, Yuandong Tian, Rui Fan, Weiwen Jin, Zhuang Hu, Zheng Yao, Shuzhong Cancer Biomark Research Article BACKGROUND: The current cervical cancer screening strategies based on Papanicolaou (Pap) and Human papillomavirus (HPV) tests receive great achievement but still exhibit many limitations in clinical practice. Exploring new biomarkers as stratified management method in HPV primary screening is becoming the tendency of current research. METHODS: Immunocytochemistry (ICC) of FHIT and C-MYC were performed on exfoliated cervical cells from 197 eligible high-risk HPV positive women. Mann-Whitney U test, Pearson Chi-Square test, logistic regression analysis and receiver operating characteristic (ROC) curves were used to assess the diagnostic efficiency. RESULTS: ICC staining intensity of FHIT and C-MYC in high-grade cervical intraepithelial neoplasia (CIN) specimens was significantly different from low-grade CIN and normal specimens. Compared with Pap test, ROC analysis of ICC in detecting high-grade CIN resulted in a larger area under the curve (AUC) (0.805 and 0.814 vs 0.723, [Formula: see text] 0.001). FHIT achieved higher sensitivity than Pap test (79.41% vs 66.67%, [Formula: see text] 0.04). Logistic regression analysis of the combination of two biomarkers led to higher AUC value, specificity and PPV than any single biomarker. CONCLUSIONS: The utility of FHIT and C-MYC ICC analysis in cervical exfoliated cells of HPV-positive women displayed superior diagnostic potential and may improve clinical performance of cervical cancer screening. IOS Press 2020-03-03 /pmc/articles/PMC7175930/ /pubmed/31771040 http://dx.doi.org/10.3233/CBM-182232 Text en © 2020 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License (CC BY-NC 4.0).
spellingShingle Research Article
Yang, Fan
Cui, Zifeng
Liao, Yuandong
Tian, Rui
Fan, Weiwen
Jin, Zhuang
Hu, Zheng
Yao, Shuzhong
FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women
title FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women
title_full FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women
title_fullStr FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women
title_full_unstemmed FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women
title_short FHIT and C-MYC expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women
title_sort fhit and c-myc expression in cervical histology and cytology as biomarkers for detecting high-grade intraepithelial neoplasia in human papillomavirus-positive women
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175930/
https://www.ncbi.nlm.nih.gov/pubmed/31771040
http://dx.doi.org/10.3233/CBM-182232
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