CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions

Background: From our previous study, we established that cyclin A1 (CCNA1) promoter methylation is strongly correlated with multistep progression of HPV-associated cervical cancer, suggesting potential use as a diagnostic maker of disease. Objectives: The purpose of the present study was to assess t...

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Main Authors: Suthipong Chujan, Nakarin Kitkumthorn, Sumalee Siriangkul, Apiwat Mutirangura
Format: Journal
Published: 2018
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spelling th-cmuir.6653943832-532782018-09-04T09:59:06Z CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions Suthipong Chujan Nakarin Kitkumthorn Sumalee Siriangkul Apiwat Mutirangura Biochemistry, Genetics and Molecular Biology Medicine Background: From our previous study, we established that cyclin A1 (CCNA1) promoter methylation is strongly correlated with multistep progression of HPV-associated cervical cancer, suggesting potential use as a diagnostic maker of disease. Objectives: The purpose of the present study was to assess the prevalence of CCNA1 promoter methylation in residual cervical cells isolated from liquid-based cytology that underwent hrHPV DNA screening for cervical cancer, and then to evaluate this marker for diagnostic accuracy using parameters like sensitivity, specificity, predictive values and likelihood ratio. Methods: In this retrospective study, histopathology was used as the gold standard method with specimens separated into the following groups: negative (n=31), low-grade squamous intraepithelial lesions (LSIL, n=34) and high-grade squamous intraepithelial lesions or worse (HSIL+, n=32). The hrHPV was detected by Hybrid Capture 2 (HC2) and CCNA1 promoter methylation was examined by CCNA1 duplex methylation specific PCR. Results: The results showed the frequencies of CCNA1 promoter methylation were 0%, 5.88% and 83.33%, while the percentages of hrHPV were 66.67%, 82.35% and 100% in the negative, LSIL and HSIL+ groups, respectively. Although hrHPV infection showed high frequency in all three groups, it could not differentiate between the different groups and grades of precancerous lesions. In contrast, CCNA1 promoter methylation clearly distinguished between negative/LSIL and HSIL+, with high levels of all statistic parameters. Conclusion: CCNA1 promoter methylation is a potential marker for distinguishing between histologic negative/LSIL and HSIL+using cervical cytology samples. 2018-09-04T09:46:16Z 2018-09-04T09:46:16Z 2014-01-01 Journal 15137368 2-s2.0-84908031784 10.7314/APJCP.2014.15.18.7971 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84908031784&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/53278
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
Suthipong Chujan
Nakarin Kitkumthorn
Sumalee Siriangkul
Apiwat Mutirangura
CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions
description Background: From our previous study, we established that cyclin A1 (CCNA1) promoter methylation is strongly correlated with multistep progression of HPV-associated cervical cancer, suggesting potential use as a diagnostic maker of disease. Objectives: The purpose of the present study was to assess the prevalence of CCNA1 promoter methylation in residual cervical cells isolated from liquid-based cytology that underwent hrHPV DNA screening for cervical cancer, and then to evaluate this marker for diagnostic accuracy using parameters like sensitivity, specificity, predictive values and likelihood ratio. Methods: In this retrospective study, histopathology was used as the gold standard method with specimens separated into the following groups: negative (n=31), low-grade squamous intraepithelial lesions (LSIL, n=34) and high-grade squamous intraepithelial lesions or worse (HSIL+, n=32). The hrHPV was detected by Hybrid Capture 2 (HC2) and CCNA1 promoter methylation was examined by CCNA1 duplex methylation specific PCR. Results: The results showed the frequencies of CCNA1 promoter methylation were 0%, 5.88% and 83.33%, while the percentages of hrHPV were 66.67%, 82.35% and 100% in the negative, LSIL and HSIL+ groups, respectively. Although hrHPV infection showed high frequency in all three groups, it could not differentiate between the different groups and grades of precancerous lesions. In contrast, CCNA1 promoter methylation clearly distinguished between negative/LSIL and HSIL+, with high levels of all statistic parameters. Conclusion: CCNA1 promoter methylation is a potential marker for distinguishing between histologic negative/LSIL and HSIL+using cervical cytology samples.
format Journal
author Suthipong Chujan
Nakarin Kitkumthorn
Sumalee Siriangkul
Apiwat Mutirangura
author_facet Suthipong Chujan
Nakarin Kitkumthorn
Sumalee Siriangkul
Apiwat Mutirangura
author_sort Suthipong Chujan
title CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions
title_short CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions
title_full CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions
title_fullStr CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions
title_full_unstemmed CCNA1 promoter methylation: A potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions
title_sort ccna1 promoter methylation: a potential marker for grading papanicolaou smear cervical squamous intraepithelial lesions
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84908031784&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/53278
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