Importance of genetic background of oxysterol signaling in cancer
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F75010330%3A_____%2F18%3A00012310" target="_blank" >RIV/75010330:_____/18:00012310 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11120/18:43916710 RIV/00216208:11140/18:10375004
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S0300908418301184?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0300908418301184?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.biochi.2018.04.023" target="_blank" >10.1016/j.biochi.2018.04.023</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Importance of genetic background of oxysterol signaling in cancer
Popis výsledku v původním jazyce
Oxysterols, oxygenated derivatives of cholesterol, are formed in the human body or ingested. Experimental evidence suggests that due to their diverse functions, e.g. modulating the activity of receptors such as liver X receptors, oxysterol-binding and metabolizing proteins, and several ATP binding cassette transporters, oxysterols may contribute to a number of human disorders including cancer. Genetic variability of oxysterol pathways represents another side of this process, affecting carcinogenesis and cancer progression. This review summarizes information about both the physiological role of oxysterol pathway genes and observed associations between their genetic variability and cancer incidence, progression, and therapy outcome. Besides candidate gene studies, results of genome-wide association studies are presented as well. The survey of available data shows some potential genetic biomarkers that, if clinically validated, may allow the stratification of individuals into genetically defined groups for prediction of individual cancer risk and subsequent screening strategies for early diagnosis.
Název v anglickém jazyce
Importance of genetic background of oxysterol signaling in cancer
Popis výsledku anglicky
Oxysterols, oxygenated derivatives of cholesterol, are formed in the human body or ingested. Experimental evidence suggests that due to their diverse functions, e.g. modulating the activity of receptors such as liver X receptors, oxysterol-binding and metabolizing proteins, and several ATP binding cassette transporters, oxysterols may contribute to a number of human disorders including cancer. Genetic variability of oxysterol pathways represents another side of this process, affecting carcinogenesis and cancer progression. This review summarizes information about both the physiological role of oxysterol pathway genes and observed associations between their genetic variability and cancer incidence, progression, and therapy outcome. Besides candidate gene studies, results of genome-wide association studies are presented as well. The survey of available data shows some potential genetic biomarkers that, if clinically validated, may allow the stratification of individuals into genetically defined groups for prediction of individual cancer risk and subsequent screening strategies for early diagnosis.
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
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Biochimie
ISSN
0300-9084
e-ISSN
1638-6183
Svazek periodika
153
Číslo periodika v rámci svazku
October
Stát vydavatele periodika
FR - Francouzská republika
Počet stran výsledku
30
Strana od-do
109-138
Kód UT WoS článku
000446007300013
EID výsledku v databázi Scopus
—