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Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer

PURPOSE: N6-methyladenosine (m6A) is the most frequent type of messenger RNA (mRNA) modification and is implicated in diverse physiological processes. The procedure of m6A RNA modification is regulated by a dynamic interaction of writers (METTL3, METTL4, METTL14, WTAP, KIAA1429), erasers (FTO, ALKBH...

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Autores principales: Ralser, Damian J., Condic, Mateja, Klümper, Niklas, Ellinger, Jörg, Staerk, Christian, Egger, Eva K., Kristiansen, Glen, Mustea, Alexander, Thiesler, Thore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129960/
https://www.ncbi.nlm.nih.gov/pubmed/35731272
http://dx.doi.org/10.1007/s00432-022-04083-1
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author Ralser, Damian J.
Condic, Mateja
Klümper, Niklas
Ellinger, Jörg
Staerk, Christian
Egger, Eva K.
Kristiansen, Glen
Mustea, Alexander
Thiesler, Thore
author_facet Ralser, Damian J.
Condic, Mateja
Klümper, Niklas
Ellinger, Jörg
Staerk, Christian
Egger, Eva K.
Kristiansen, Glen
Mustea, Alexander
Thiesler, Thore
author_sort Ralser, Damian J.
collection PubMed
description PURPOSE: N6-methyladenosine (m6A) is the most frequent type of messenger RNA (mRNA) modification and is implicated in diverse physiological processes. The procedure of m6A RNA modification is regulated by a dynamic interaction of writers (METTL3, METTL4, METTL14, WTAP, KIAA1429), erasers (FTO, ALKBH5), and readers (HNRNPA2B1, HNRNPC, YTHDC1, YTHDC1, YTHDF1-3). In the oncological context, alterations in m6A were identified to be critically involved in tumorigenesis, proliferation, angiogenesis, and drug resistance across diverse cancer entities including endometrial cancer (EC). METHODS: In this study, we comprehensively examined the protein expression of m6A writers, readers and erasers by immunohistochemical staining in a cohort of N = 65 EC patients. Protein expression data were analyzed with regard to clinical outcomes. RESULTS: We identified enhanced protein expression levels of METTL3, METTL14, FTO, HNRNPA2B1, and HNRNPC, respectively to be of prognostic value and linked to a shortened overall survival in EC. CONCLUSION: Overall, our study points toward dysregulated m6A modification in EC and its possibility to serve as a promising prognostic biomarker.
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spelling pubmed-101299602023-04-27 Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer Ralser, Damian J. Condic, Mateja Klümper, Niklas Ellinger, Jörg Staerk, Christian Egger, Eva K. Kristiansen, Glen Mustea, Alexander Thiesler, Thore J Cancer Res Clin Oncol Research PURPOSE: N6-methyladenosine (m6A) is the most frequent type of messenger RNA (mRNA) modification and is implicated in diverse physiological processes. The procedure of m6A RNA modification is regulated by a dynamic interaction of writers (METTL3, METTL4, METTL14, WTAP, KIAA1429), erasers (FTO, ALKBH5), and readers (HNRNPA2B1, HNRNPC, YTHDC1, YTHDC1, YTHDF1-3). In the oncological context, alterations in m6A were identified to be critically involved in tumorigenesis, proliferation, angiogenesis, and drug resistance across diverse cancer entities including endometrial cancer (EC). METHODS: In this study, we comprehensively examined the protein expression of m6A writers, readers and erasers by immunohistochemical staining in a cohort of N = 65 EC patients. Protein expression data were analyzed with regard to clinical outcomes. RESULTS: We identified enhanced protein expression levels of METTL3, METTL14, FTO, HNRNPA2B1, and HNRNPC, respectively to be of prognostic value and linked to a shortened overall survival in EC. CONCLUSION: Overall, our study points toward dysregulated m6A modification in EC and its possibility to serve as a promising prognostic biomarker. Springer Berlin Heidelberg 2022-06-22 2023 /pmc/articles/PMC10129960/ /pubmed/35731272 http://dx.doi.org/10.1007/s00432-022-04083-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Ralser, Damian J.
Condic, Mateja
Klümper, Niklas
Ellinger, Jörg
Staerk, Christian
Egger, Eva K.
Kristiansen, Glen
Mustea, Alexander
Thiesler, Thore
Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer
title Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer
title_full Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer
title_fullStr Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer
title_full_unstemmed Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer
title_short Comprehensive immunohistochemical analysis of N6-methyladenosine (m6A) writers, erasers, and readers in endometrial cancer
title_sort comprehensive immunohistochemical analysis of n6-methyladenosine (m6a) writers, erasers, and readers in endometrial cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129960/
https://www.ncbi.nlm.nih.gov/pubmed/35731272
http://dx.doi.org/10.1007/s00432-022-04083-1
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