Suppr超能文献

N6-甲基腺苷(m6A)调控基因将肝细胞癌分为三种亚型。

N6-methyladenosine (m6A) regulatory gene divides hepatocellular carcinoma into three subtypes.

作者信息

Wei Jie, Fang Da Lang, Zhou Weijie, He Yong Fei

机构信息

Department of Hematology, Baise People's Hospital, Baise, China.

Department of Breast and Thyroid Surgery, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.

出版信息

J Gastrointest Oncol. 2021 Aug;12(4):1860-1872. doi: 10.21037/jgo-21-378.

Abstract

BACKGROUND

The N6-methyladenosine (m6A) plays an important role in epigenetic modification and tumor progression, but the modulations of m6A in hepatocellular carcinoma (HCC) have not been determined while the relationship between m6A regulation and immune cell infiltration remains unclear.

METHODS

This study investigated the modification patterns of m6A by analyzing HCC samples from The Cancer Genome Atlas (TCGA) database and the Gene Expression Omnibus (GEO) dataset, and performed molecular typing based on the characteristics of immune cell infiltration. The m6Ascore was also constructed to quantify m6A modifications and predict the immunotherapy response and prognosis of HCC patients.

RESULTS

Of the 364 samples, 31 (8.52%) were genetically altered in the m6A regulatory gene, with the highest frequency of mutations in , , and . Three distinct molecular subtypes of m6A were identified in 590 HCC samples, which were associated with different immune cell infiltrates: immunodepletion type, immune activation type, and immune immunity type. According to the construction of the m6Ascore system in the m6A genotype, HCC patients could be divided into high and low groups. The m6A modified pattern, characterized by immune immunity and immune failure, showed a lower score and a better prognosis. However, the immune-activated type of m6A had a higher score and a poorer prognosis. Further analysis showed that the m6Ascore was correlated with tumor mutation burden (TMB), and the higher the TMB, the worse the prognosis. m6Ascore was also correlated with the expression of cytotoxic T-lymphocyte-associated protein 4 (CTAL-4), and the higher the score, the higher the expression of HCC in patients.

CONCLUSIONS

HCC has a unique m6A modification pattern, and 3 different m6A subtypes help to classify HCC, provide knowledge of drug regimens for immunotherapy, and can be used to predict treatment response and prognosis.

摘要

背景

N6-甲基腺苷(m6A)在表观遗传修饰和肿瘤进展中起重要作用,但肝细胞癌(HCC)中m6A的调控尚未明确,且m6A调控与免疫细胞浸润之间的关系仍不清楚。

方法

本研究通过分析来自癌症基因组图谱(TCGA)数据库和基因表达综合数据库(GEO)的数据集中的HCC样本,研究m6A的修饰模式,并基于免疫细胞浸润特征进行分子分型。还构建了m6A评分来量化m6A修饰,并预测HCC患者的免疫治疗反应和预后。

结果

在364个样本中,31个(8.52%)在m6A调控基因中发生了基因改变,其中 、 和 的突变频率最高。在590个HCC样本中鉴定出三种不同的m6A分子亚型,它们与不同的免疫细胞浸润相关:免疫耗竭型、免疫激活型和免疫豁免型。根据m6A基因型构建的m6A评分系统,HCC患者可分为高分组和低分组。以免疫豁免和免疫衰竭为特征的m6A修饰模式得分较低,预后较好。然而,免疫激活型m6A得分较高,预后较差。进一步分析表明,m6A评分与肿瘤突变负荷(TMB)相关,TMB越高,预后越差。m6A评分还与细胞毒性T淋巴细胞相关蛋白4(CTAL-4)的表达相关,评分越高,HCC患者中的表达越高。

结论

HCC具有独特的m6A修饰模式,三种不同的m6A亚型有助于对HCC进行分类,为免疫治疗提供用药方案知识,并可用于预测治疗反应和预后。

相似文献

1
N6-methyladenosine (m6A) regulatory gene divides hepatocellular carcinoma into three subtypes.
J Gastrointest Oncol. 2021 Aug;12(4):1860-1872. doi: 10.21037/jgo-21-378.
2
Comprehensive Analysis of N6-methyladenosine Modification Patterns Associated With Multiomic Characteristics of Bladder Cancer.
Front Med (Lausanne). 2021 Dec 23;8:757432. doi: 10.3389/fmed.2021.757432. eCollection 2021.
3
N6-methyladenosine with immune infiltration and PD-L1 in hepatocellular carcinoma: novel perspective to personalized diagnosis and treatment.
Front Endocrinol (Lausanne). 2023 Jul 3;14:1153802. doi: 10.3389/fendo.2023.1153802. eCollection 2023.
4
The m6A methylation landscape stratifies hepatocellular carcinoma into 3 subtypes with distinct metabolic characteristics.
Cancer Biol Med. 2020 Nov 15;17(4):937-952. doi: 10.20892/j.issn.2095-3941.2020.0402. Epub 2020 Dec 15.
5
m6A Regulator-Associated Modification Patterns and Immune Infiltration of the Tumor Microenvironment in Hepatocarcinoma.
Front Cell Dev Biol. 2021 Jul 2;9:687756. doi: 10.3389/fcell.2021.687756. eCollection 2021.
7
M6A regulator-mediated immune infiltration and methylation modification in hepatocellular carcinoma microenvironment and immunotherapy.
Front Pharmacol. 2022 Nov 10;13:1052177. doi: 10.3389/fphar.2022.1052177. eCollection 2022.
9
Analysis of N6-Methyladenosine Modification Patterns and Tumor Immune Microenvironment in Pancreatic Adenocarcinoma.
Front Genet. 2022 Jan 3;12:752025. doi: 10.3389/fgene.2021.752025. eCollection 2021.

引用本文的文献

2
Comprehensive analysis of m6A RNA methylation regulators in esophageal carcinoma.
Transl Cancer Res. 2024 Jan 31;13(1):381-393. doi: 10.21037/tcr-23-910. Epub 2024 Jan 18.
3
Pan-cancer analysis revealed prognosis value and immunological relevance of RAMPs.
Heliyon. 2024 Jan 18;10(3):e24849. doi: 10.1016/j.heliyon.2024.e24849. eCollection 2024 Feb 15.
4
m5C methylation modification guides the prognostic value and immune landscapes in acute myeloid leukemia.
Aging (Albany NY). 2023 Sep 25;15(18):9858-9876. doi: 10.18632/aging.205059.
5
6
The m6A/m5C/m1A Regulated Gene Signature Predicts the Prognosis and Correlates With the Immune Status of Hepatocellular Carcinoma.
Front Immunol. 2022 Jun 27;13:918140. doi: 10.3389/fimmu.2022.918140. eCollection 2022.

本文引用的文献

2
Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.
CA Cancer J Clin. 2021 May;71(3):209-249. doi: 10.3322/caac.21660. Epub 2021 Feb 4.
3
CTNNB1 mutation suppresses infiltration of immune cells in hepatocellular carcinoma through miRNA-mediated regulation of chemokine expression.
Int Immunopharmacol. 2020 Dec;89(Pt A):107043. doi: 10.1016/j.intimp.2020.107043. Epub 2020 Oct 8.
4
Roles of long non-coding RNAs and emerging RNA-binding proteins in innate antiviral responses.
Theranostics. 2020 Jul 23;10(20):9407-9424. doi: 10.7150/thno.48520. eCollection 2020.
5
Liver Cancer Immunity.
Hepatology. 2021 Jan;73 Suppl 1(Suppl 1):86-103. doi: 10.1002/hep.31416. Epub 2020 Nov 7.
7
The RNA modification N-methyladenosine as a novel regulator of the immune system.
Nat Immunol. 2020 May;21(5):501-512. doi: 10.1038/s41590-020-0650-4. Epub 2020 Apr 13.
8
Molecular characterization and clinical relevance of mA regulators across 33 cancer types.
Mol Cancer. 2019 Sep 14;18(1):137. doi: 10.1186/s12943-019-1066-3.
10
mA mRNA demethylase FTO regulates melanoma tumorigenicity and response to anti-PD-1 blockade.
Nat Commun. 2019 Jun 25;10(1):2782. doi: 10.1038/s41467-019-10669-0.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验