A Novel RNA Methylation-Related Prognostic Signature and its Tumor Microenvironment Characterization in Hepatocellular Carcinoma.

IF 2.7 4区 医学 Q3 ONCOLOGY Technology in Cancer Research & Treatment Pub Date : 2024-01-01 DOI:10.1177/15330338241276895
Luzheng Liu, Jiacheng Chen, Fei Ye, Yanggang Yan, Yong Wang, Jincai Wu
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Abstract

Introduction: Hepatocellular carcinoma (HCC) is one of the most common malignant tumors of the digestive system. RNA methylation plays an important role in tumorigenesis and metastasis, which could alter gene expression and even function at multiple levels, such as RNA splicing, stability, translocation, and translation. In this study, we aimed to conduct a comprehensive analysis of RNA methylation-related genes (RMGs) in HCC and their relationship with survival and clinical features.

Methods: A retrospective analysis was performed using publicly available HCC-related datasets. The differentially expressed genes (DEGs) between HCC and controls were identified from TCGA-LlHC and intersected with RMGs to obtain differentially expressed RNA methylation-related genes (DERMGs). Regression analysis was used to screen for prognostic genes and construct risk models. Simultaneously, clinical, immune infiltration and therapeutic efficacy analyses were performed. Finally, multivariate cox regression was used to identify independent risk factors, and quantitative real-time polymerase chain reaction (qRT-PCR) was used to validate the expression levels of the core genes of the model.

Results: A 21-gene risk model for HCC was established with excellent performance based on ROC curves and survival analysis. Risk scores correlated with tumor grade, pathologic T, and TNM stage. Immune infiltration analysis showed correlations with immune scores, 11 immune cells, and 30 immune checkpoints. Low-risk patients showed a higher susceptibility to immunotherapy. The risk score and TNM stage were independent prognostic factors. qRT-PCR confirmed higher expression of PRDM9, ALPP, and GAD1 in HCC.

Conclusions: This study identified RNA methylation-related signature genes in HCC and constructed a risk model that predicts patient outcomes and reflects the immune microenvironment. Prognostic genes are involved in complex regulatory mechanisms, which may be useful for cancer diagnosis, prognosis, and therapy.

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肝细胞癌中与 RNA 甲基化相关的新型预后特征及其肿瘤微环境特征描述
简介:肝细胞癌(HCC)是消化系统最常见的恶性肿瘤之一:肝细胞癌(HCC)是消化系统最常见的恶性肿瘤之一。RNA 甲基化在肿瘤发生和转移过程中起着重要作用,可在多个水平上改变基因表达甚至功能,如 RNA 剪接、稳定性、转位和翻译。在这项研究中,我们旨在对HCC中的RNA甲基化相关基因(RMGs)及其与生存和临床特征的关系进行全面分析:方法:我们利用公开的 HCC 相关数据集进行了回顾性分析。从TCGA-LlHC中确定了HCC和对照组之间的差异表达基因(DEGs),并将其与RMGs交叉以获得差异表达的RNA甲基化相关基因(DERMGs)。回归分析用于筛选预后基因和构建风险模型。同时,还进行了临床、免疫浸润和疗效分析。最后,研究人员利用多变量考克斯回归确定了独立的风险因素,并利用实时定量聚合酶链反应(qRT-PCR)验证了模型核心基因的表达水平:结果:根据ROC曲线和生存分析,建立的21个基因的HCC风险模型表现优异。风险评分与肿瘤分级、病理 T 和 TNM 分期相关。免疫浸润分析显示与免疫评分、11种免疫细胞和30个免疫检查点相关。低风险患者对免疫疗法的易感性更高。qRT-PCR证实PRDM9、ALPP和GAD1在HCC中表达较高:本研究发现了 HCC 中与 RNA 甲基化相关的特征基因,并构建了一个可预测患者预后并反映免疫微环境的风险模型。预后基因涉及复杂的调控机制,可能有助于癌症诊断、预后和治疗。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
202
审稿时长
2 months
期刊介绍: Technology in Cancer Research & Treatment (TCRT) is a JCR-ranked, broad-spectrum, open access, peer-reviewed publication whose aim is to provide researchers and clinicians with a platform to share and discuss developments in the prevention, diagnosis, treatment, and monitoring of cancer.
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