Epigenome dysregulation in cholangiocarcinoma
Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt
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Epigenome dysregulation in cholangiocarcinoma. / O'Rourke, Colm J; Munoz-Garrido, Patricia; Aguayo, Esmeralda L; Andersen, Jesper B.
I: BBA Molecular Basis of Disease, Bind 1864, Nr. 4, Part B, 2018, s. 1423-1434.Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt
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TY - JOUR
T1 - Epigenome dysregulation in cholangiocarcinoma
AU - O'Rourke, Colm J
AU - Munoz-Garrido, Patricia
AU - Aguayo, Esmeralda L
AU - Andersen, Jesper B
N1 - Copyright © 2017 Elsevier B.V. All rights reserved.
PY - 2018
Y1 - 2018
N2 - Epigenomics is a fast-evolving field of research that has lately attracted considerable interest, mainly due to the reversibility of epigenetic marks. Clinically, among solid tumors, the field is still limited. In cholangiocarcinoma (CCA) it is well known that the epigenetic landscape is deregulated both during carcinogenesis and disease progression as a consequence of aberrant mechanisms leading to genome instability. In this article, we will briefly review the molecular alterations that have been described in the transformation of normal cholangiocytes into malignant derivatives, focusing on the role of non-coding RNA (ncRNA) interactions, DNA methylation, post-translational modifications (PTMs) of histones and chromatin remodeling complexes.
AB - Epigenomics is a fast-evolving field of research that has lately attracted considerable interest, mainly due to the reversibility of epigenetic marks. Clinically, among solid tumors, the field is still limited. In cholangiocarcinoma (CCA) it is well known that the epigenetic landscape is deregulated both during carcinogenesis and disease progression as a consequence of aberrant mechanisms leading to genome instability. In this article, we will briefly review the molecular alterations that have been described in the transformation of normal cholangiocytes into malignant derivatives, focusing on the role of non-coding RNA (ncRNA) interactions, DNA methylation, post-translational modifications (PTMs) of histones and chromatin remodeling complexes.
KW - Journal Article
KW - Review
U2 - 10.1016/j.bbadis.2017.06.014
DO - 10.1016/j.bbadis.2017.06.014
M3 - Review
C2 - 28645654
VL - 1864
SP - 1423
EP - 1434
JO - B B A - Molecular Basis of Disease
JF - B B A - Molecular Basis of Disease
SN - 0925-4439
IS - 4, Part B
ER -
ID: 182354750