{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T08:27:35Z","timestamp":1786955255717,"version":"build-2736575974"},"reference-count":84,"publisher":"MDPI AG","issue":"16","license":[{"start":{"date-parts":[[2026,8,16]],"date-time":"2026-08-16T00:00:00Z","timestamp":1786838400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cells"],"abstract":"<jats:p>As a key N6-methyladenosine (m6A)-binding protein, YT521-B Homology (YTH) Domain-Containing Protein 2 (YTHDC2) plays a central role in the epitranscriptomic regulatory network. This protein specifically recognizes and binds to m6A modification sites on RNA molecules through its highly conserved YTH domain. This recognition exhibits high selectivity and affinity, thereby enabling precise control over the fate of target RNAs. At the molecular level, YTHDC2 is widely involved in various stages of the RNA life cycle, including core biological processes such as RNA splicing and processing, nuclear\u2013cytoplasmic transport, translational efficiency regulation, and RNA decay. In recent years, accumulating evidence indicates that YTHDC2 participates in a variety of pathophysiological processes in an m6A-dependent manner. However, the robustness of evidence regarding YTHDC2 is heterogeneous across disease contexts. While certain pathologies are supported by rigorous mechanistic validation, others rely primarily on expression correlations or bioinformatic analyses. This review systematically synthesizes current knowledge regarding the multifaceted roles of YTHDC2 in disease progression, prognosis, and therapy, offering a comprehensive framework to guide future investigations.<\/jats:p>","DOI":"10.3390\/cells15161467","type":"journal-article","created":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T08:05:41Z","timestamp":1786953941000},"page":"1467","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["The m6A Reader YTHDC2: Molecular Mechanisms and Regulatory Networks in Disease Pathogenesis"],"prefix":"10.3390","volume":"15","author":[{"ORCID":"https:\/\/orcid.org\/0009-0000-7193-1310","authenticated-orcid":false,"given":"Yanying","family":"Hu","sequence":"first","affiliation":[{"name":"Institute of Preventive Medicine, School of Public Health, Dali University, No. 22, Wanhua Road, Dali 671000, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qi","family":"Zhou","sequence":"additional","affiliation":[{"name":"Institute of Preventive Medicine, School of Public Health, Dali University, No. 22, Wanhua Road, Dali 671000, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ning","family":"Xu","sequence":"additional","affiliation":[{"name":"Institute of Preventive Medicine, School of Public Health, Dali University, No. 22, Wanhua Road, Dali 671000, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0001-2242-3712","authenticated-orcid":false,"given":"Ning","family":"Du","sequence":"additional","affiliation":[{"name":"Institute of Preventive Medicine, School of Public Health, Dali University, No. 22, Wanhua Road, Dali 671000, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shuangping","family":"Yang","sequence":"additional","affiliation":[{"name":"Institute of Preventive Medicine, School of Public Health, Dali University, No. 22, Wanhua Road, Dali 671000, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4278-2509","authenticated-orcid":false,"given":"Shiyan","family":"Gu","sequence":"additional","affiliation":[{"name":"Institute of Preventive Medicine, School of Public Health, Dali University, No. 22, Wanhua Road, Dali 671000, China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2026,8,16]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"e2022024118","DOI":"10.1073\/pnas.2022024118","article-title":"N6-methyladenosine modification of HCV RNA genome regulates cap-independent IRES-mediated translation via YTHDC2 recognition","volume":"118","author":"Kim","year":"2021","journal-title":"Proc. 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