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Epigenetic Alterations in Pancreatic Cancer Metastasis

Authors: Sarah S. Wang; Jihao Xu; Keely Y. Ji; Chang-Il Hwang;

Epigenetic Alterations in Pancreatic Cancer Metastasis

Abstract

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.

Keywords

Epigenomics, Carcinogenesis, pancreatic cancer, Review, Epigenesis, Genetic, Histones, Mice, 2.1 Biological and endogenous factors, Neoplasm Metastasis, Cancer, DNA methylation, Cell Differentiation, Biological Sciences, Prognosis, Bioinformatics and computational biology, QR1-502, Chromatin, Gene Expression Regulation, Neoplastic, Pancreatic Ductal, Disease Progression, Carcinoma, Pancreatic Ductal, Oncology and Carcinogenesis, Medical biotechnology, 610, Adenocarcinoma, Microbiology, Pancreatic Cancer, Rare Diseases, Cancer Genomics, Genetic, Genetics, biochemistry, metastasis, Animals, Humans, Neoplastic, Biomedical and Clinical Sciences, epigenetics, Human Genome, Carcinoma, DNA Methylation, 4.1 Discovery and preclinical testing of markers and technologies, Pancreatic Neoplasms, Orphan Drug, Gene Expression Regulation, Biochemistry and cell biology, Mutation, Biochemistry and Cell Biology, Digestive Diseases, Biomarkers, Epigenesis, Transcription Factors

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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    42
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
42
Top 10%
Top 10%
Top 1%
Green
gold