<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(24)</volume><submitter>Li Z</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Squamous cell carcinoma (SCC) and adenocarcinoma (AC) are the two main pathological types of esophageal cancer (EC), which differ in molecular features, genetic variation, and treatment sensitivity. However, as a key process in tumorigenesis and development, the role of N6-methyladenosine (m6A) regulators in esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC) is not fully understood.&lt;h4>Methods&lt;/h4>This study systematically compared the role of m6A regulators of ESCC and EAC in terms of molecular characteristics, immuno-oncology characteristics, and clinical relevance, and validated our findings in a long-term follow-up patient cohort.&lt;h4>Results&lt;/h4>There were many differences in m6A regulators between ESCC and EAC in terms of expression patterns, genetic variation, association with tumor pathways, immune signatures, and immunotherapy sensitivity. Furthermore, &lt;i>VIRMA&lt;/i> was identified as a factor with opposite functional and prognostic effects in ESCC and EAC. ESCC patients with high &lt;i>VIRMA&lt;/i> expression and EAC patients with low &lt;i>VIRMA&lt;/i> expression had a better prognosis. Single-center data showed that low expression of &lt;i>FTO&lt;/i> may be associated with superior immunotherapy efficacy in ESCC patients.&lt;h4>Conclusions&lt;/h4>The results herein provide novel ideas for understanding the tumor characteristics, occurrence, and development of ESCC and EAC, and suggest new targets for the treatment and intervention of EC.</pubmed_abstract><journal>Annals of translational medicine</journal><pagination>1347</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9843396</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance.</pubmed_title><pmcid>PMC9843396</pmcid><pubmed_authors>Yin X</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Zheng C</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Li B</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance.</name><description>&lt;h4>Background&lt;/h4>Squamous cell carcinoma (SCC) and adenocarcinoma (AC) are the two main pathological types of esophageal cancer (EC), which differ in molecular features, genetic variation, and treatment sensitivity. However, as a key process in tumorigenesis and development, the role of N6-methyladenosine (m6A) regulators in esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC) is not fully understood.&lt;h4>Methods&lt;/h4>This study systematically compared the role of m6A regulators of ESCC and EAC in terms of molecular characteristics, immuno-oncology characteristics, and clinical relevance, and validated our findings in a long-term follow-up patient cohort.&lt;h4>Results&lt;/h4>There were many differences in m6A regulators between ESCC and EAC in terms of expression patterns, genetic variation, association with tumor pathways, immune signatures, and immunotherapy sensitivity. Furthermore, &lt;i>VIRMA&lt;/i> was identified as a factor with opposite functional and prognostic effects in ESCC and EAC. ESCC patients with high &lt;i>VIRMA&lt;/i> expression and EAC patients with low &lt;i>VIRMA&lt;/i> expression had a better prognosis. Single-center data showed that low expression of &lt;i>FTO&lt;/i> may be associated with superior immunotherapy efficacy in ESCC patients.&lt;h4>Conclusions&lt;/h4>The results herein provide novel ideas for understanding the tumor characteristics, occurrence, and development of ESCC and EAC, and suggest new targets for the treatment and intervention of EC.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T08:29:25.347Z</modification><creation>2025-04-04T08:29:25.347Z</creation></dates><accession>S-EPMC9843396</accession><cross_references><pubmed>36660671</pubmed><doi>10.21037/atm-22-5895</doi></cross_references></HashMap>