NSUN6-mediated 5-methylcytosine modification of NDRG1 mRNA promotes radioresistance in cervical cancer

抗辐射性 辐射敏感性 生物 癌症研究 癌症 核糖核酸 信使核糖核酸 基因沉默 小RNA 分子生物学 遗传学 放射治疗 基因 医学 内科学 细胞培养
作者
Min Yu,Mengdong Ni,Fei Xu,Chaohua Liu,Lihua Chen,Jiana Li,Siyu Xia,Yixin Diao,Jiaxin Chen,Jun Zhu,Xiaohua Wu,Min Tang,Jiajia Li,Guihao Ke
出处
期刊:Molecular Cancer [BioMed Central]
卷期号:23 (1) 被引量:12
标识
DOI:10.1186/s12943-024-02055-2
摘要

Abstract Background Radioresistance is the leading cause of death in advanced cervical cancer (CC). Dysregulation of RNA modification has recently emerged as a regulatory mechanism in radiation and drug resistance. We aimed to explore the biological function and clinical significance of 5-methylcytosine (m 5 C) in cervical cancer radiosensitivity. Methods The abundance of RNA modification in radiotherapy-resistant and sensitive CC specimens was quantified by liquid chromatography-tandem mass spectrometry. The essential RNA modification-related genes involved in CC radiosensitivity were screened via RNA sequencing. The effect of NSUN6 on radiosensitivity was verified in CC cell lines, cell-derived xenograft (CDX), and 3D bioprinted patient-derived organoid (PDO). The mechanisms of NSUN6 in regulating CC radiosensitivity were investigated by integrative m 5 C sequencing, mRNA sequencing, and RNA immunoprecipitation. Results We found a higher abundance of m 5 C modification in resistant CC samples, and NSUN6 was the essential m 5 C-regulating gene concerning radiosensitivity. NSUN6 overexpression was clinically correlated with radioresistance and poor prognosis in cervical cancer. Functionally, higher NSUN6 expression was associated with radioresistance in the 3D PDO model of cervical cancer. Moreover, silencing NSUN6 increased CC radiosensitivity in vivo and in vitro. Mechanistically, NDRG1 was one of the downstream target genes of NSUN6 identified by integrated m 5 C-seq, mRNA-seq, and functional validation. NSUN6 promoted the m 5 C modification of NDRG1 mRNA, and the m 5 C reader ALYREF bound explicitly to the m 5 C-labeled NDRG1 mRNA and enhanced NDRG1 mRNA stability. NDRG1 overexpression promoted homologous recombination-mediated DNA repair, which in turn led to radioresistance in cervical cancer. Conclusions Aberrant m 5 C hypermethylation and NSUN6 overexpression drive resistance to radiotherapy in cervical cancer. Elevated NSUN6 expression promotes radioresistance in cervical cancer by activating the NSUN6/ALYREF-m 5 C-NDRG1 pathway. The low expression of NSUN6 in cervical cancer indicates sensitivity to radiotherapy and a better prognosis.
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