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The YTH Domain-containing Protein Family: Emerging Players in Immunomodulation and Tumour Immunotherapy Targets

Overview
Journal Clin Transl Med
Publisher Wiley
Specialty General Medicine
Date 2024 Aug 13
PMID 39135292
Authors
Affiliations
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Abstract

Background: The modification of N6-methyladenosine (m6A) plays a pivotal role in tumor by altering both innate and adaptive immune systems through various pathways, including the regulation of messenger RNA. The YTH domain protein family, acting as "readers" of m6A modifications, affects RNA splicing, stability, and immunogenicity, thereby playing essential roles in immune regulation and antitumor immunity. Despite their significance, the impact of the YTH domain protein family on tumor initiation and progression, as well as their involvement in tumor immune regulation and therapy, remains underexplored and lacks comprehensive review.

Conclusion: This review introduces the molecular characteristics of the YTH domain protein family and their physiological and pathological roles in biological behavior, emphasizing their mechanisms in regulating immune responses and antitumor immunity. Additionally, the review discusses the roles of the YTH domain protein family in immune-related diseases and tumor resistance, highlighting that abnormal expression or dysfunction of YTH proteins is closely linked to tumor resistance.

Key Points: This review provides an in-depth understanding of the YTH domain protein family in immune regulation and antitumor immunity, suggesting new strategies and directions for immunotherapy of related diseases. These insights not only deepen our comprehension of m6A modifications and YTH protein functions but also pave the way for future research and clinical applications.

Citing Articles

Emerging roles of N-methyladenosine in arsenic-induced toxicity.

Li R, Wu C, Zhao Y, Jiang S, Huang J, Huo X Heliyon. 2024; 10(22):e40473.

PMID: 39641074 PMC: 11617730. DOI: 10.1016/j.heliyon.2024.e40473.


The YTH domain-containing protein family: Emerging players in immunomodulation and tumour immunotherapy targets.

Li F, Zeng C, Liu J, Wang L, Yuan X, Yuan L Clin Transl Med. 2024; 14(8):e1784.

PMID: 39135292 PMC: 11319238. DOI: 10.1002/ctm2.1784.

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