دورية أكاديمية

The identification and validation of EphA7 hypermethylation, a novel biomarker, in cervical cancer.

التفاصيل البيبلوغرافية
العنوان: The identification and validation of EphA7 hypermethylation, a novel biomarker, in cervical cancer.
المؤلفون: Zhang W; Department of Laboratory Medicine, Tianjin Medical University, Tianjin, China., Cao H; Department of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China., Yang J; Department of Laboratory Medicine, Tianjin Medical University, Tianjin, China., Zhao J; Department of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China., Liang Z; Department of Otorhinolaryngology, Tianjin Medical University General Hospital, Tianjin, China., Kang X; Department of Medical Image, Tianjin Medical University, Tianjin, China., Wang R; Department of Laboratory Medicine, Tianjin Medical University, Tianjin, China. wangrong825@tmu.edu.cn.
المصدر: BMC cancer [BMC Cancer] 2022 Jun 09; Vol. 22 (1), pp. 636. Date of Electronic Publication: 2022 Jun 09.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2407 (Electronic) Linking ISSN: 14712407 NLM ISO Abbreviation: BMC Cancer Subsets: MEDLINE
أسماء مطبوعة: Original Publication: London : BioMed Central, [2001-
مواضيع طبية MeSH: DNA Methylation* , Receptor, EphA7*/genetics , Uterine Cervical Neoplasms*/diagnosis , Uterine Cervical Neoplasms*/genetics, Biomarkers, Tumor ; Cell Line, Tumor ; Female ; Gene Expression Regulation, Neoplastic ; Humans
مستخلص: Background: Aberrant methylation of EphA7 has been reported in the process of carcinogenesis but not in cervical cancer. Therefore, an integration study was performed to explore the association between EphA7 hypermethylation and cervical cancer and validate the potential value of EphA7 hypermethylation in the diagnosis of cervical cancer.
Methods: We performed an integration study to identify and validate the association between EphA7 methylation and cervical cancer. First, data on EphA7 methylation and expression in cervical cancer were extracted and analyzed via bioinformatics tools. Subsequently, CRISPR-based methylation perturbation tools (dCas9-Tet1/DNMT3a) were constructed to further demonstrate the association between DNA methylation and EphA7 expression. Ultimately, the clinical value of EphA7 methylation in cervical cancer was validated in cervical tissues and Thinprep cytologic test (TCT) samples by methylation-specific PCR (MSP) and quantitative methylation-specific PCR (QMSP), respectively.
Results: Pooled analysis showed that EphA7 promoter methylation levels were significantly increased in cervical cancer compared to normal tissues (P < 0.001) and negatively correlated with EphA7 expression. These prediction results were subsequently confirmed in cell lines; moreover, CRISPR-based methylation perturbation tools (dCas9-Tet1/DNMT3a) demonstrated that DNA methylation participates in the regulation of EphA7 expression directly. Consistent with these findings, the methylation level and the positive rate of EphA7 gradually increased with severity from normal to cancer stages in TCT samples (P < 0.01).
Conclusions: EphA7 hypermethylation is present in cervical cancer and is a potential biomarker for the diagnosis of cervical cancer.
(© 2022. The Author(s).)
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فهرسة مساهمة: Keywords: CRISPR-dCas9; Cervical cancer; DNA methylation; EphA7
المشرفين على المادة: 0 (Biomarkers, Tumor)
EC 2.7.10.1 (Receptor, EphA7)
تواريخ الأحداث: Date Created: 20220610 Date Completed: 20220613 Latest Revision: 20220716
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC9185921
DOI: 10.1186/s12885-022-09653-7
PMID: 35681118
قاعدة البيانات: MEDLINE
الوصف
تدمد:1471-2407
DOI:10.1186/s12885-022-09653-7