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The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance

BACKGROUND: 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-methyladenosin...

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Autores principales: Li, Zhe, Zheng, Chunyan, Huang, Liquan, Yin, Xiaoyang, Wang, Zhongtang, Liu, Chengxin, Li, Baosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843396/
https://www.ncbi.nlm.nih.gov/pubmed/36660671
http://dx.doi.org/10.21037/atm-22-5895
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author Li, Zhe
Zheng, Chunyan
Huang, Liquan
Yin, Xiaoyang
Wang, Zhongtang
Liu, Chengxin
Li, Baosheng
author_facet Li, Zhe
Zheng, Chunyan
Huang, Liquan
Yin, Xiaoyang
Wang, Zhongtang
Liu, Chengxin
Li, Baosheng
author_sort Li, Zhe
collection PubMed
description BACKGROUND: 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. METHODS: 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. RESULTS: 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, VIRMA was identified as a factor with opposite functional and prognostic effects in ESCC and EAC. ESCC patients with high VIRMA expression and EAC patients with low VIRMA expression had a better prognosis. Single-center data showed that low expression of FTO may be associated with superior immunotherapy efficacy in ESCC patients. CONCLUSIONS: 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.
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spelling pubmed-98433962023-01-18 The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance Li, Zhe Zheng, Chunyan Huang, Liquan Yin, Xiaoyang Wang, Zhongtang Liu, Chengxin Li, Baosheng Ann Transl Med Original Article BACKGROUND: 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. METHODS: 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. RESULTS: 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, VIRMA was identified as a factor with opposite functional and prognostic effects in ESCC and EAC. ESCC patients with high VIRMA expression and EAC patients with low VIRMA expression had a better prognosis. Single-center data showed that low expression of FTO may be associated with superior immunotherapy efficacy in ESCC patients. CONCLUSIONS: 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. AME Publishing Company 2022-12 /pmc/articles/PMC9843396/ /pubmed/36660671 http://dx.doi.org/10.21037/atm-22-5895 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Li, Zhe
Zheng, Chunyan
Huang, Liquan
Yin, Xiaoyang
Wang, Zhongtang
Liu, Chengxin
Li, Baosheng
The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance
title The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance
title_full The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance
title_fullStr The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance
title_full_unstemmed The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance
title_short The landscape of m6A regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance
title_sort landscape of m6a regulators in esophageal cancer: molecular characteristics, immuno-oncology features, and clinical relevance
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843396/
https://www.ncbi.nlm.nih.gov/pubmed/36660671
http://dx.doi.org/10.21037/atm-22-5895
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