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The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients

RNA methylation at the nitrogen sixth of adenosine (m(6)A, N(6)-methyladenosine) is the most abundant RNA modification which plays a crucial role in all RNA metabolic aspects. Recently, m(6)A modification has been assigned to mediate the biological processes of cancer cells, but their significance i...

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Autores principales: Romanowska, Kamila, Rawłuszko-Wieczorek, Agnieszka A., Marczak, Łukasz, Kosińska, Agnieszka, Suchorska, Wiktoria M., Golusiński, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235215/
https://www.ncbi.nlm.nih.gov/pubmed/34207099
http://dx.doi.org/10.3390/biom11060908
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author Romanowska, Kamila
Rawłuszko-Wieczorek, Agnieszka A.
Marczak, Łukasz
Kosińska, Agnieszka
Suchorska, Wiktoria M.
Golusiński, Wojciech
author_facet Romanowska, Kamila
Rawłuszko-Wieczorek, Agnieszka A.
Marczak, Łukasz
Kosińska, Agnieszka
Suchorska, Wiktoria M.
Golusiński, Wojciech
author_sort Romanowska, Kamila
collection PubMed
description RNA methylation at the nitrogen sixth of adenosine (m(6)A, N(6)-methyladenosine) is the most abundant RNA modification which plays a crucial role in all RNA metabolic aspects. Recently, m(6)A modification has been assigned to mediate the biological processes of cancer cells, but their significance in HNSCC development is still poorly described. Thus, the main aim of this study was to globally quantify m(6)A modification by the mass spectrometry approach and determine the mRNA expression level of selected m(6)A RNA methyltransferase (METTL3), demethylase (FTO), and m(6)A readers (YTHDF2, YTHDC2) in 45 HNSCC patients and 4 cell lines (FaDu, Detroit 562, A-253 and SCC-15) using qPCR. In the results, we have not observed differences in the global amount of m(6)A modification and the mRNA level of the selected genes between the cancerous and paired-matched histopathologically unchanged tissues from 45 HNSCC patients. However, we have found a positive correlation between selected RNA methylation machinery genes expression and m(6)A abundance on total RNA and characterized the transcript level of those genes in the HNSCC cell lines. Moreover, the lack of global m(6)A differences between cancerous and histopathologically unchanged tissues suggests that m(6)A alterations in specific RNA sites may specifically influence HNSCC tumorigenesis.
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spelling pubmed-82352152021-06-27 The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients Romanowska, Kamila Rawłuszko-Wieczorek, Agnieszka A. Marczak, Łukasz Kosińska, Agnieszka Suchorska, Wiktoria M. Golusiński, Wojciech Biomolecules Article RNA methylation at the nitrogen sixth of adenosine (m(6)A, N(6)-methyladenosine) is the most abundant RNA modification which plays a crucial role in all RNA metabolic aspects. Recently, m(6)A modification has been assigned to mediate the biological processes of cancer cells, but their significance in HNSCC development is still poorly described. Thus, the main aim of this study was to globally quantify m(6)A modification by the mass spectrometry approach and determine the mRNA expression level of selected m(6)A RNA methyltransferase (METTL3), demethylase (FTO), and m(6)A readers (YTHDF2, YTHDC2) in 45 HNSCC patients and 4 cell lines (FaDu, Detroit 562, A-253 and SCC-15) using qPCR. In the results, we have not observed differences in the global amount of m(6)A modification and the mRNA level of the selected genes between the cancerous and paired-matched histopathologically unchanged tissues from 45 HNSCC patients. However, we have found a positive correlation between selected RNA methylation machinery genes expression and m(6)A abundance on total RNA and characterized the transcript level of those genes in the HNSCC cell lines. Moreover, the lack of global m(6)A differences between cancerous and histopathologically unchanged tissues suggests that m(6)A alterations in specific RNA sites may specifically influence HNSCC tumorigenesis. MDPI 2021-06-18 /pmc/articles/PMC8235215/ /pubmed/34207099 http://dx.doi.org/10.3390/biom11060908 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Romanowska, Kamila
Rawłuszko-Wieczorek, Agnieszka A.
Marczak, Łukasz
Kosińska, Agnieszka
Suchorska, Wiktoria M.
Golusiński, Wojciech
The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients
title The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients
title_full The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients
title_fullStr The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients
title_full_unstemmed The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients
title_short The m(6)A RNA Modification Quantity and mRNA Expression Level of RNA Methylation-Related Genes in Head and Neck Squamous Cell Carcinoma Cell Lines and Patients
title_sort m(6)a rna modification quantity and mrna expression level of rna methylation-related genes in head and neck squamous cell carcinoma cell lines and patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235215/
https://www.ncbi.nlm.nih.gov/pubmed/34207099
http://dx.doi.org/10.3390/biom11060908
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