METTL1通过ATF4 mRNA的m7G修饰协调皮肤鳞状细胞癌的进展。

IF 7 2区 生物学 Q1 CELL BIOLOGY Cell Death Discovery Pub Date : 2025-01-27 DOI:10.1038/s41420-025-02304-3
Xinru Zhang, Tong Chen, Fanrong Zhang, Huanhuan Shi, Xiang Li, Zhijuan Wang, Dong Wang, Chao Hou
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引用次数: 0

摘要

甲基转移酶样1 (METTL1)介导的m7G修饰在各种RNA物种中都很常见,包括mrna、tRNAs、rnas和miRNAs。最近的证据表明,这种修饰与几种癌症的发展有关,使其成为癌症治疗的一个有希望的目标。然而,m7G修饰在皮肤鳞状细胞癌(cSCC)中的具体作用尚不清楚。在这项研究中,我们观察到METTL1在cSCC肿瘤和细胞系中的水平明显升高。抑制METTL1可降低cSCC细胞的存活、迁移、侵袭和异种移植物肿瘤生长。在机制上,通过RNA测序、m7G甲基化免疫沉淀(MeRIP)-qPCR和mRNA稳定性分析,我们发现METTL1负责ATF4 mRNA的m7G修饰,导致ATF4表达增加。重要的是,我们证明了这种修饰依赖于METTL1的甲基转移酶活性。此外,我们观察到cSCC肿瘤中ATF4表达与METTL1水平呈正相关。有趣的是,恢复ATF4在cSCC细胞中的表达不仅可以促进糖酵解,还可以逆转METTL1敲低的抗肿瘤作用。总之,我们的研究结果强调了METTL1和m7G修饰在cSCC肿瘤发生中的关键作用,为未来的cSCC治疗提供了一个有希望的靶点。
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METTL1 coordinates cutaneous squamous cell carcinoma progression via the m7G modification of the ATF4 mRNA.

Methyltransferase-like 1 (METTL1)-mediated m7G modification is a common occurrence in various RNA species, including mRNAs, tRNAs, rRNAs, and miRNAs. Recent evidence suggests that this modification is linked to the development of several cancers, making it a promising target for cancer therapy. However, the specific role of m7G modification in cutaneous squamous cell carcinoma (cSCC) is not well understood. In this study, we observed conspicuously elevated levels of METTL1 in cSCC tumors and cell lines. Inhibiting METTL1 led to reduced survival, migration, invasion, and xenograft tumor growth in cSCC cells. Mechanistically, through a combination of RNA sequencing, m7G methylated immunoprecipitation (MeRIP)-qPCR, and mRNA stability assays, we discovered that METTL1 is responsible for the m7G modification of ATF4 mRNA, leading to increased expression of ATF4. Importantly, we demonstrated that this modification is dependent on the methyltransferase activity of METTL1. Additionally, we observed a positive association between ATF4 expression and METTL1 levels in cSCC tumors. Intriguingly, restoring ATF4 expression in cSCC cells not only promoted glycolysis but also reversed the anti-tumor effects of METTL1 knockdown. In conclusion, our results underscore the critical role of METTL1 and m7G modification in cSCC tumorigenesis, suggesting a promising target for future cSCC therapies.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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