4.6 Article

Analysis of N6-Methyladenosine Methylome in Adenocarcinoma of Esophagogastric Junction

Journal

FRONTIERS IN GENETICS
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2021.787800

Keywords

epigenomics; adenocarcinoma of esophagogastric junction; m(6)A methylation; diagnosis; treatment

Funding

  1. Jiangsu Innovative Team Leading Talent Fund [CXTDC2016006, QNRC2016446]
  2. Jiangsu 333 Talent Fund [BRA2020016]
  3. Jiangsu Provincial Key Research and Development Special Fund [BE2015666]
  4. Jiangsu Six High Peak Talent Fund [WSW-205, WSW236]
  5. Zhenjiang Key Research and Development Fund [SH2021038]
  6. Suqian Science and Technology Support Project Fund [K201907]

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This study systematically analyzed the m(6)A mRNA modification pattern in adenocarcinoma at the esophagogastric junction, identifying numerous new m(6)A peaks and their relationship with cancer-related pathways in AEG samples. The differential expression of mRNA transcripts in AEG showed hypermethylated or hypomethylated m(6)A peaks.
Background: From previous studies, we found that there are more than 100 types of RNA modifications in RNA molecules. m(6)A methylation is the most common. The incidence rate of adenocarcinoma of the esophagogastric junction (AEG) at home and abroad has increased faster than that of stomach cancer at other sites in recent years. Here, we systematically analyze the modification pattern of m(6)A mRNA in adenocarcinoma at the esophagogastric junction.Methods: m(6)A sequencing, RNA sequencing, and bioinformatics analysis were used to describe the m(6)A modification pattern in adenocarcinoma and normal tissues at the esophagogastric junction.Results: In AEG samples, a total of 4,775 new m(6)A peaks appeared, and 3,054 peaks disappeared. The unique m6A-related genes in AEG are related to cancer-related pathways. There are hypermethylated or hypomethylated m(6)A peaks in AEG in differentially expressed mRNA transcripts.Conclusion: This study preliminarily constructed the first m(6)A full transcriptome map of human AEG. This has a guiding role in revealing the mechanism of m(6)A-mediated gene expression regulation.

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