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http://purl.uniprot.org/citations/32514824http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/32514824http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

To investigate the possibility of using the methylation level of PAX1/ZNF582 gene as molecular marker to differentiate the progression of cervical cancer.

Methods

From January 2016 to March 2018, 150 patients, who were admitted to Cervical Disease Diagnosis and Treatment Center of Xuzhu Maternity and Child Care Hospital, were enrolled in this study. Patients were classified into chronic cervicitis (for 19 cases), low-grade squamous intraepithelial lesion (LSIL) (18 cases), high-grade squamous intraepithelial lesion (HSIL) (37 cases) and squamous cell carcinoma (SCC) (31 cases). All patients underwent several tests including Thin-prep cytology test (TCT), HPV DNA detection and detection of methylation level of PAX1/ZNF582 genes.

Results

For diagnosis of HSIL, the area under curve (AUC) was 0.878 (95% CI 0.806 ~ 0.950); the threshold for PAX1 was 12.285, the sensitivity and specificity were 91.9% and 72.8%, respectively. The AUC of ZNF582 gene detection was 0.900 (95% CI 0.842 ~ 0.959), the threshold was 11.56, while the sensitivity and specificity were 97.3% and 76.7%, respectively. Among various tests we conducted, PAX gene detection methods showed the highest specificity (97.30%). PAX1/ZNF582 gene detection method demonstrated the highest accuracy.

Conclusions

For patients with high-grade cervical lesion and cervical cancer, the methylation level of PAX1/ZNF582 gene could be applied as a noteworthy biomarker for diagnosis and for cervical cancer classification."xsd:string
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http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Fu M."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Huang H."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Liu J."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Liang H."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Wei Y."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Xiao J."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Zhao K."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/author"Li G.L."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/name"Clin Transl Oncol"xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/pages"283-288"xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/title"The application value of PAX1 and ZNF582 gene methylation in high grade intraepithelial lesion and cervical cancer."xsd:string
http://purl.uniprot.org/citations/32514824http://purl.uniprot.org/core/volume"23"xsd:string
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