m6A调节因子对头颈部鳞状细胞癌预后的综合研究。

Jingning Cheng, Yong Lyu, Ziyan Cheng
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引用次数: 0

摘要

头颈部鳞状细胞癌(HNSCC)的早期发现对临床预后有重要影响。N6-甲基腺苷(m6A)参与肿瘤发生和发展的转录后调控。本研究探讨了m6A调节靶点在HNSCC中的预后和生物学功能。收集来自TCGA-HNSCC和GSE23036数据集的RNA-Seq表达数据和临床信息。肿瘤组织中IGF2BP2和IGF2BP3的mRNA水平显著上调。从m6A2Target数据库获得的IGF2BP2和IGF2BP3的潜在靶标的差异表达和功能富集分析表明,它们在细胞周期相关途径中显著富集。进行Cox回归分析以建立包括PLAU、LPIN1和AURKA的三种mRNA特征。在外部数据集GSE41613中验证了预后效果。进一步的研究表明,在临床亚组中,三种信使核糖核酸特征与生存率显著相关。ROC曲线、Harrell一致性指数和决策曲线比较用于比较先前研究中三种信使核糖核酸标记与其他标记的预测效果,表明三种信使信使核糖核酸信号对HNSCC患者的预后具有更好的预测效果。用qRT-PCR和Western blot在HNSCC细胞系中验证了这三种mRNA特征表达。序列分析表明,在PLAU、LPIN1和AURKA基因上均存在m6A修饰位点。总之,三种信使核糖核酸标记已被证明可用于评估HNSCC的预后并有助于HNSCC的个性化治疗,并且IGB2BP2/3与HNSCC的细胞周期有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive Investigation of m6A Regulators for Prognosis in Head and Neck Squamous Cell Carcinoma.

The early detection of head and neck squamous cell carcinoma (HNSCC) has an important impact on the clinical prognosis. N6-methyladenosine (m6A) is involved in the post-transcriptional regulation of tumorigenesis and development. In this study, the prognosis and biological functions of m6A regulator targets in HNSCC were explored. RNA-Seq expression data and clinical information from TCGA-HNSCC and GSE23036 datasets were collected. The mRNA levels of IGF2BP2 and IGF2BP3 in tumor tissues were significantly up-regulated. Differential expression and functional enrichment analysis of potential targets for IGF2BP2 and IGF2BP3 obtained from the m6A2Target database showed that they were significantly enriched in cell cycle-related pathways. The Cox regression analysis was performed to establish a three-mRNA signature including PLAU, LPIN1 and AURKA. The prognostic effect was verified in the external dataset GSE41613. Further studies revealed that the three-mRNA signature was significantly associated with survival in the clinical subgroup. The ROC curve, Harrell consistency index and decision curve comparison used to compare the predictive effect of the three-mRNA signature and the other signatures in previous studies showed that the three-mRNA signature had better predictive effect on the prognosis of HNSCC patients. The three-mRNA signature expression were verified in HNSCC cell lines with qRT-PCR and Western blot. Sequence analysis showed that m6A-modification sites existed on PLAU, LPIN1 and AURKA genes. In conclusion, the three-mRNA signature has been proved to be useful on evaluating the prognosis and contributing to the personalized treatment of HNSCC, and IGB2BP2/3 were related to the cell cycle in HNSCC.

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