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Epigenetic Alterations in Pancreatic Cancer Metastasis

Pancreatic cancer is the third leading cause of cancer-related deaths in the United States. Pancreatic ductal adenocarcinoma (PDA) is the most common (90%) and aggressive type of pancreatic cancer. Genomic analyses of PDA specimens have identified the recurrent genetic mutations that drive PDA initi...

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Autores principales: Wang, Sarah S., Xu, Jihao, Ji, Keely Y., Hwang, Chang-Il
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394313/
https://www.ncbi.nlm.nih.gov/pubmed/34439749
http://dx.doi.org/10.3390/biom11081082
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author Wang, Sarah S.
Xu, Jihao
Ji, Keely Y.
Hwang, Chang-Il
author_facet Wang, Sarah S.
Xu, Jihao
Ji, Keely Y.
Hwang, Chang-Il
author_sort Wang, Sarah S.
collection PubMed
description Pancreatic cancer is the third leading cause of cancer-related deaths in the United States. Pancreatic ductal adenocarcinoma (PDA) is the most common (90%) and aggressive type of pancreatic cancer. Genomic analyses of PDA specimens have identified the recurrent genetic mutations that drive PDA initiation and progression. However, the underlying mechanisms that further drive PDA metastasis remain elusive. Despite many attempts, no recurrent genetic mutation driving PDA metastasis has been found, suggesting that PDA metastasis is driven by epigenetic fluctuations rather than genetic factors. Therefore, establishing epigenetic mechanisms of PDA metastasis would facilitate the development of successful therapeutic interventions. In this review, we provide a comprehensive overview on the role of epigenetic mechanisms in PDA as a critical contributor on PDA progression and metastasis. In particular, we explore the recent advancements elucidating the role of nucleosome remodeling, histone modification, and DNA methylation in the process of cancer metastasis.
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spelling pubmed-83943132021-08-28 Epigenetic Alterations in Pancreatic Cancer Metastasis Wang, Sarah S. Xu, Jihao Ji, Keely Y. Hwang, Chang-Il Biomolecules Review Pancreatic cancer is the third leading cause of cancer-related deaths in the United States. Pancreatic ductal adenocarcinoma (PDA) is the most common (90%) and aggressive type of pancreatic cancer. Genomic analyses of PDA specimens have identified the recurrent genetic mutations that drive PDA initiation and progression. However, the underlying mechanisms that further drive PDA metastasis remain elusive. Despite many attempts, no recurrent genetic mutation driving PDA metastasis has been found, suggesting that PDA metastasis is driven by epigenetic fluctuations rather than genetic factors. Therefore, establishing epigenetic mechanisms of PDA metastasis would facilitate the development of successful therapeutic interventions. In this review, we provide a comprehensive overview on the role of epigenetic mechanisms in PDA as a critical contributor on PDA progression and metastasis. In particular, we explore the recent advancements elucidating the role of nucleosome remodeling, histone modification, and DNA methylation in the process of cancer metastasis. MDPI 2021-07-22 /pmc/articles/PMC8394313/ /pubmed/34439749 http://dx.doi.org/10.3390/biom11081082 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 Review
Wang, Sarah S.
Xu, Jihao
Ji, Keely Y.
Hwang, Chang-Il
Epigenetic Alterations in Pancreatic Cancer Metastasis
title Epigenetic Alterations in Pancreatic Cancer Metastasis
title_full Epigenetic Alterations in Pancreatic Cancer Metastasis
title_fullStr Epigenetic Alterations in Pancreatic Cancer Metastasis
title_full_unstemmed Epigenetic Alterations in Pancreatic Cancer Metastasis
title_short Epigenetic Alterations in Pancreatic Cancer Metastasis
title_sort epigenetic alterations in pancreatic cancer metastasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394313/
https://www.ncbi.nlm.nih.gov/pubmed/34439749
http://dx.doi.org/10.3390/biom11081082
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