Association between PEG3 DNA methylation and high-grade cervical intraepithelial neoplasia.

Journal Article (Journal Article)

BACKGROUND: Epigenetic mechanisms are hypothesized to contribute substantially to the progression of cervical intraepithelial neoplasia (CIN) to cervical cancer, although empirical data are limited. METHODS: Women (n = 419) were enrolled at colposcopic evaluation at Duke Medical Center in Durham, North Carolina. Human papillomavirus (HPV) was genotyped by HPV linear array and CIN grade was ascertained by biopsy pathologic review. DNA methylation was measured at differentially methylated regions (DMRs) regulating genomic imprinting of the IGF2/H19, IGF2AS, MESTIT1/MEST, MEG3, PLAGL1/HYMAI, KvDMR and PEG10, PEG3 imprinted domains, using Sequenom-EpiTYPER assays. Logistic regression models were used to evaluate the associations between HPV infection, DMR methylation and CIN risk overall and by race. RESULTS: Of the 419 participants, 20 had CIN3+, 52 had CIN2, and 347 had ≤ CIN1 (CIN1 and negative histology). The median participant age was 28.6 (IQR:11.6) and 40% were African American. Overall, we found no statistically significant association between altered methylation in selected DMRs and CIN2+ compared to ≤CIN1. Similarly, there was no significant association between DMR methylation and CIN3+ compared to ≤CIN2. Restricting the outcome to CIN2+ cases that were HR-HPV positive and p16 staining positive, we found a significant association with PEG3 DMR methylation (OR: 1.56 95% CI: 1.03-2.36). CONCLUSIONS: While the small number of high-grade CIN cases limit inferences, our findings suggest an association between altered DNA methylation at regulatory regions of PEG3 and high grade CIN in high-risk HPV positive cases.

Full Text

Duke Authors

Cited Authors

  • Bosire, C; Vidal, AC; Smith, JS; Jima, D; Huang, Z; Skaar, D; Valea, F; Bentley, R; Gradison, M; Yarnall, KSH; Ford, A; Overcash, F; Murphy, SK; Hoyo, C

Published Date

  • June 13, 2021

Published In

Volume / Issue

  • 16 / 1

Start / End Page

  • 42 -

PubMed ID

  • 34120615

Pubmed Central ID

  • PMC8201933

International Standard Serial Number (ISSN)

  • 1750-9378

Digital Object Identifier (DOI)

  • 10.1186/s13027-021-00382-3

Language

  • eng

Conference Location

  • England