Epstein–Barr Virus Promotes Gastric Cancer Progression by Modulating m6A-Dependent YTHDF1–TSC22D1 Axis

  • Yea Rim An
  • , Jaehun Jung
  • , Kyeong Min Kwon
  • , Jun Yeob Kim
  • , Min Hyeok Lee
  • , Ju Yeon Lee
  • , Minho Lee
  • , Suk Kyeong Lee

Research output: Contribution to journalArticlepeer-review

Abstract

Epstein–Barr virus (EBV) infection is closely associated with gastric cancer, yet its role in m6A-dependent gene regulation remains poorly understood. In this study, we investigated how EBV infection alters the m6A methylation pattern in gastric cancer cells and examined its impact on TSC22D1 mRNA stability through interaction with the m6A reader protein YTHDF1. m6A RNA immunoprecipitation sequencing (MeRIP-seq) revealed a significant reduction in m6A methylation of TSC22D1 in EBV-infected gastric cancer cells (AGS-EBV) compared with EBV-negative cells (AGS). Moreover, YTHDF1 knockdown increased both the stability and expression of TSC22D1. These findings demonstrate that YTHDF1 binds to TSC22D1 mRNA and promotes its m6A-dependent degradation. Collectively, our results suggest that EBV infection modulates m6A modification to regulate gene stability and identify the YTHDF1–TSC22D1 axis as a potential therapeutic target in EBV-associated gastric cancer.

Original languageEnglish
Article number2820
JournalMicroorganisms
Volume13
Issue number12
DOIs
StatePublished - Dec 2025

Keywords

  • Epstein–Barr virus
  • TSC22D1
  • YTHDF1
  • epitranscriptomics
  • gastric cancer
  • m6A modification

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