4.5 Article

The Value and Clinical Significance of ZNF582 Gene Methylation in the Diagnosis of Cervical Cancer

Journal

ONCOTARGETS AND THERAPY
Volume 14, Issue -, Pages 403-411

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/OTT.S277445

Keywords

cervical cancer; ZNF582 gene; promoter methylation; HPV16/18; gene expression

Funding

  1. International Science and Technology Collaboration Projector of Xinjiang Production and Construction Corps [2019BC007]
  2. National Natural Science Foundation of China [U1503125, 81660462]
  3. Youth Project Development and Regeneration Key Laboratory of Sichuan Province
  4. General Project Scientific Research Fund of Chengdu Medical College [SYS1807]
  5. Xinjiang Production and Construction Corps Key Areas Innovation Team Project [2018CB002]

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The study aimed to investigate the association between ZNF582 gene methylation and cervical cancer, as well as its correlation with high risk HPV16/18 infection. The findings showed that ZNF582 gene methylation had high specificity and sensitivity in detecting highly diseased cervical lesions, and ZNF582 protein was highly expressed in cervical cancer tissues but with low mRNA expression.
Introduction: The aim of this study was to determine whether ZNF582 gene methylation and tissue protein expression can be used as a tool with high sensitivity and specificity for cervical cancer screening. We analyzed the correlation between promoter methylation of ZNF582 gene and cervical cancer and high risk HPV16/18 infection. Methods: Tissue samples of normal cervical or chronic cervicitis (n=51), CIN (cervical intraepithelial neoplasia) (n=35), and cervical carcinoma (n=68) were tested for HPV16/18 infection by polymerase chain reaction (PCR). We also detected the methylation status of the ZNF582 gene promoter in the same tissues by methylation-specific PCR (MSP), then analyzed the correlation between ZNF582 promoter methylation and HPV16/18 infection. Immunohistochemistry was used to analyze ZNF582 gene expression in 152 cervical tissues. We detected ZNF582 mRNA expression in cervical tissues (including cancer and non-cancer) by real-time fluorescence quantitative PCR (qPCR). Results: Among 93 high-grade cervical lesions (CINII and above) and cervical cancer samples, 57 cases were positive for HPV16/18 infection and 36 cases were negative. ZNF582 gene methylation occurred in 9 out of 51 cases in normal cervical tissues (17.6%), 16 of 35 cases in CIN tissues (45.7%), and 50 of 68 cases in cervical cancer (73.5%). The differences in methylation rate of the three groups were statistically significant (P<0.05). The ZNF582 methylation rate in the positive HPV16/18 infection group was 73.7%, while the negative group was 63.9%. Compared with normal tissues, ZNF582 protein was highly expressed in cervical cancer tissues, but mRNA expression was low. Conclusion: While ZNF582 protein is highly expressed in cervical cancer tissues, it was not sufficient for use as a standard for cervical cancer staging. On the other hand, ZNF582 promoter methylation had high specificity and sensitivity in detecting CINII and highly diseased cervical lesions and could be used as a diagnostic marker for cervical cancer of women.

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