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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8235215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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