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NAT10通过对ELANE mRNA进行ac4C修饰来抑制喉鳞状细胞癌的细胞焦亡。

NAT10 inhibits the pyroptosis of laryngeal squamous cell carcinoma through ac4C modification of ELANE mRNA.

作者信息

Yu Yafang, Yan Jianwen

机构信息

Department of Otolaryngology, Fujian Medical University Union Hospital, No.6, Xuefu South Road, Minhou County, Fuzhou, Fujian, 350000, China.

Department of Otolaryngology, Fuzhou Second Hospital, Fuzhou, Fujian, China.

出版信息

BMC Cancer. 2025 May 30;25(1):970. doi: 10.1186/s12885-025-14352-0.

Abstract

BACKGROUND

Laryngeal squamous cell carcinoma (LSCC) is the most common type of head and neck malignancy. NAT10 is a catalytic enzyme for ac4C and is involved in the progression of a variety of cancers. This study aimed to explore the effects and potential mechanisms of NAT10 in LSCC.

METHODS

Pyroptosis was assessed by measuring the release of lactic dehydrogenase, pyroptosis rate, and pyroptosis-related proteins. The RNA and protein levels were detected by quantitative real-time PCR and western blot, respectively. Potential mechanisms were validated using flow cytometry, ac4C dot blot, methylated RNA immunoprecipitation (MeRIP), RIP, and Dual-Luciferase Reporter Assay experiments.

RESULTS

The result showed that the levels of NAT10 in LSCC tissues and cells were elevated and positively correlated with tumor grading and clinical staging. Knockdown of NAT10 promoted the pyroptosis of LSCC cells. NAT10 directly interacted with ELANE, suppressed the stability of the ELANE mRNA. NAT10 inhibited pyroptosis in LSCC by downregulating the ELANE expression in vivo and in vitro.

CONCLUSION

NAT10 inhibited the pyroptosis of LSCC cells and contributed to LSCC progression by suppressing ELANE mRNA stability in ac4C modification manner, indicating that the NAT10-ac4C-ELANE axis might be a potential target for LSCC.

摘要

背景

喉鳞状细胞癌(LSCC)是头颈部最常见的恶性肿瘤类型。NAT10是一种催化ac4C的酶,参与多种癌症的进展。本研究旨在探讨NAT10在LSCC中的作用及潜在机制。

方法

通过检测乳酸脱氢酶释放量、焦亡率和焦亡相关蛋白来评估焦亡。分别用定量实时PCR和蛋白质印迹法检测RNA和蛋白质水平。使用流式细胞术、ac4C斑点印迹、甲基化RNA免疫沉淀(MeRIP)、RIP和双荧光素酶报告基因检测实验验证潜在机制。

结果

结果显示,LSCC组织和细胞中NAT10水平升高,且与肿瘤分级和临床分期呈正相关。敲低NAT10可促进LSCC细胞的焦亡。NAT10直接与ELANE相互作用,抑制ELANE mRNA的稳定性。NAT10在体内和体外通过下调ELANE表达抑制LSCC中的焦亡。

结论

NAT10通过以ac4C修饰方式抑制ELANE mRNA稳定性来抑制LSCC细胞的焦亡,并促进LSCC进展,表明NAT10-ac4C-ELANE轴可能是LSCC的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac5b/12123832/ba261a4319b9/12885_2025_14352_Fig1_HTML.jpg

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