YTHDF2 in hepatocellular carcinoma: Bridging m6A modification and cancer progression

Abstract YTH N6‐methyladenosine RNAbinding protein F2 (YTHDF2) is an N6‐methyladenosine (m6A) reader protein that mainly regulates the stability of methylated transcripts through mRNA decay. In the liver, YTHDF2 is involved in metabolic homeostasis, oxidative stress responses, and immune regulation. Altered YTHDF2 expression has also been reported in hepatocellular carcinoma (HCC), where its effects appear to depend on the target transcript and cellular context. This review summarizes the molecular functions of YTHDF2 in m6A recognition, RNA stability, and hepatic metabolism. We then discuss its expression patterns in HCC and its reported roles in inflammation, oxidative stress, lipid metabolism, and cancer‐related signaling. The upstream factors that regulate YTHDF2 and its major downstream targets are also reviewed, together with its links to immune and metabolic pathways. Finally, we examine current evidence for YTHDF2 as a possible biomarker and therapeutic target and discuss the limitations that still need to be addressed before clinical application.

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Publication Details

Journal
Open Research (University of Surrey)
Published
2026-10-27
DOI
https://doi.org/10.1002/viw2.70222
Primary Topic
RNA modifications and cancer
Type
article
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article

YTHDF2 in hepatocellular carcinoma: Bridging m6A modification and cancer progression

Weihong Ge, Dongxue Ge, Sijie Zang, Haobin Shen et al.
2 links
Open Research (University of Surrey)
RNA modifications and cancer
article

YTHDF2 in hepatocellular carcinoma: Bridging m6A modification and cancer progression

Weihong Ge, Dongxue Ge, Sijie Zang, Haobin Shen, Jinglin Wang, Li Li, Dayu Chen, Wanqi Yang
article en

Abstract

Abstract YTH N6‐methyladenosine RNAbinding protein F2 (YTHDF2) is an N6‐methyladenosine (m6A) reader protein that mainly regulates the stability of methylated transcripts through mRNA decay. In the liver, YTHDF2 is involved in metabolic homeostasis, oxidative stress responses, and immune regulation. Altered YTHDF2 expression has also been reported in hepatocellular carcinoma (HCC), where its effects appear to depend on the target transcript and cellular context. This review summarizes the molecular functions of YTHDF2 in m6A recognition, RNA stability, and hepatic metabolism. We then discuss its expression patterns in HCC and its reported roles in inflammation, oxidative stress, lipid metabolism, and cancer‐related signaling. The upstream factors that regulate YTHDF2 and its major downstream targets are also reviewed, together with its links to immune and metabolic pathways. Finally, we examine current evidence for YTHDF2 as a possible biomarker and therapeutic target and discuss the limitations that still need to be addressed before clinical application.

Open Research (University of Surrey)
Macau University of Science and Technology (MO), China Pharmaceutical University (CN), Nanjing Drum Tower Hospital (CN), Nanjing Medical University (CN)
Good health and well-being
Openalex Percentile: Top 22%
RNA modifications and cancer
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YTHDF2 in hepatocellular carcinoma: Bridging m6A modification and cancer progression — Weihong Ge, Dongxue Ge, et al. · Open Research (University of Surrey) (2026) | TGRS Research Map | TGRS