DNA methylation and chromatin modifiers in colorectal cancer.
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F19%3A00518158" target="_blank" >RIV/68378041:_____/19:00518158 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11110/19:10394229 RIV/00216208:11140/19:10394229
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S0098299719300081?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0098299719300081?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.mam.2019.04.002" target="_blank" >10.1016/j.mam.2019.04.002</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
DNA methylation and chromatin modifiers in colorectal cancer.
Popis výsledku v původním jazyce
Colorectal carcinogenesis is a multistep process involving the accumulation of genetic alterations over time that ultimately leads to disease progression and metastasis. Binding of transcription factors to gene promoter regions alone cannot explain the complex regulation pattern of gene expression during this process. It is the chromatin structure that allows for a high grade of regulatory flexibility for gene expression. Posttranslational modifications on histone proteins such as acetylation, methylation, or phosphorylation determine the accessibility of transcription factors to DNA. DNA methylation, a chemical modification of DNA that modulates chromatin structure and gene transcription acts in concert with these chromatin conformation alterations. Another epigenetic mechanism regulating gene expression is represented by small non-coding RNAs. Only very recently epigenetic alterations have been included in molecular subtype classification of colorectal cancer (CRC). In this chapter, we will provide examples of the different epigenetic players, focus on their role for epithelial-mesenchymal transition and metastatic processes and discuss their prognostic value in CRC.
Název v anglickém jazyce
DNA methylation and chromatin modifiers in colorectal cancer.
Popis výsledku anglicky
Colorectal carcinogenesis is a multistep process involving the accumulation of genetic alterations over time that ultimately leads to disease progression and metastasis. Binding of transcription factors to gene promoter regions alone cannot explain the complex regulation pattern of gene expression during this process. It is the chromatin structure that allows for a high grade of regulatory flexibility for gene expression. Posttranslational modifications on histone proteins such as acetylation, methylation, or phosphorylation determine the accessibility of transcription factors to DNA. DNA methylation, a chemical modification of DNA that modulates chromatin structure and gene transcription acts in concert with these chromatin conformation alterations. Another epigenetic mechanism regulating gene expression is represented by small non-coding RNAs. Only very recently epigenetic alterations have been included in molecular subtype classification of colorectal cancer (CRC). In this chapter, we will provide examples of the different epigenetic players, focus on their role for epithelial-mesenchymal transition and metastatic processes and discuss their prognostic value in CRC.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30101 - Human genetics
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Molecular Aspects of Medicine
ISSN
0098-2997
e-ISSN
—
Svazek periodika
69
Číslo periodika v rámci svazku
SI
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
20
Strana od-do
73-92
Kód UT WoS článku
000486385900008
EID výsledku v databázi Scopus
2-s2.0-85064905503