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Visfatin and global histone H3K9me levels in colon cancer

BACKGROUND: Visfatin is considered to be a biomarker in various types of cancers, including colon cancer. Moreover, evidence for epigenetic mechanism must be reported for an association between visfatin level and colon cancer. Therefore, this study was designed to investigate the status of visfatin...

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Detalles Bibliográficos
Autores principales: Al Abdulsalam, Eman A., Al Harithy, Rowyda N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143622/
https://www.ncbi.nlm.nih.gov/pubmed/34008459
http://dx.doi.org/10.1080/07853890.2021.1925737
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author Al Abdulsalam, Eman A.
Al Harithy, Rowyda N.
author_facet Al Abdulsalam, Eman A.
Al Harithy, Rowyda N.
author_sort Al Abdulsalam, Eman A.
collection PubMed
description BACKGROUND: Visfatin is considered to be a biomarker in various types of cancers, including colon cancer. Moreover, evidence for epigenetic mechanism must be reported for an association between visfatin level and colon cancer. Therefore, this study was designed to investigate the status of visfatin expression and the global histone three modifications in colon cancerous tissue. METHODS: Colon cancerous tissue and paired adjacent non-cancerous tissue from 30 patients were used to determine the global histone three modifications using Western blot. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to assess visfatin's expression level in tissues. RESULTS: The visfatin and the global H3K9me expression levels were significantly higher in colon cancerous tissue than in the paired adjacent non-cancerous tissue. CONCLUSION: The present study makes a crucial noteworthy contribution to visfatin effect on colon cancer development via H3K9me.
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spelling pubmed-81436222021-06-07 Visfatin and global histone H3K9me levels in colon cancer Al Abdulsalam, Eman A. Al Harithy, Rowyda N. Ann Med Oncology BACKGROUND: Visfatin is considered to be a biomarker in various types of cancers, including colon cancer. Moreover, evidence for epigenetic mechanism must be reported for an association between visfatin level and colon cancer. Therefore, this study was designed to investigate the status of visfatin expression and the global histone three modifications in colon cancerous tissue. METHODS: Colon cancerous tissue and paired adjacent non-cancerous tissue from 30 patients were used to determine the global histone three modifications using Western blot. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to assess visfatin's expression level in tissues. RESULTS: The visfatin and the global H3K9me expression levels were significantly higher in colon cancerous tissue than in the paired adjacent non-cancerous tissue. CONCLUSION: The present study makes a crucial noteworthy contribution to visfatin effect on colon cancer development via H3K9me. Taylor & Francis 2021-05-19 /pmc/articles/PMC8143622/ /pubmed/34008459 http://dx.doi.org/10.1080/07853890.2021.1925737 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Oncology
Al Abdulsalam, Eman A.
Al Harithy, Rowyda N.
Visfatin and global histone H3K9me levels in colon cancer
title Visfatin and global histone H3K9me levels in colon cancer
title_full Visfatin and global histone H3K9me levels in colon cancer
title_fullStr Visfatin and global histone H3K9me levels in colon cancer
title_full_unstemmed Visfatin and global histone H3K9me levels in colon cancer
title_short Visfatin and global histone H3K9me levels in colon cancer
title_sort visfatin and global histone h3k9me levels in colon cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143622/
https://www.ncbi.nlm.nih.gov/pubmed/34008459
http://dx.doi.org/10.1080/07853890.2021.1925737
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