Many Ways to the Cell Cycle Exit after Inhibition of CDK4/6
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F23%3A00617303" target="_blank" >RIV/68378050:_____/23:00617303 - isvavai.cz</a>
Výsledek na webu
<a href="https://foliabiologica.lf1.cuni.cz/69/5/0194/" target="_blank" >https://foliabiologica.lf1.cuni.cz/69/5/0194/</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.14712/fb2023069050194" target="_blank" >10.14712/fb2023069050194</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Many Ways to the Cell Cycle Exit after Inhibition of CDK4/6
Popis výsledku v původním jazyce
Cyclin-dependent kinases (CDKs) are master regulators of proliferation, and therefore they represent attractive targets for cancer therapy. Development of selective CDK4/6 inhibitors including palbociclib revolutionized the treatment of advanced HR+/HER2– breast cancer. Inhibition of CDK4/6 leads to cell cycle arrest in G0/G1 phase and eventually to a permanent cell cycle exit called senescence. One of the main features of the senescence is an increased cell size. For many years, it was believed that the non-dividing cells simply continue to grow and as a result, they become excessively large. There is now emerging evidence that the increased cell size is a cause rather than consequence of the cell cycle arrest. This review aims to summarize recent advances in our understanding of senescence induction, in particular that resulting from treatment with CDK4/6 inhibitors.
Název v anglickém jazyce
Many Ways to the Cell Cycle Exit after Inhibition of CDK4/6
Popis výsledku anglicky
Cyclin-dependent kinases (CDKs) are master regulators of proliferation, and therefore they represent attractive targets for cancer therapy. Development of selective CDK4/6 inhibitors including palbociclib revolutionized the treatment of advanced HR+/HER2– breast cancer. Inhibition of CDK4/6 leads to cell cycle arrest in G0/G1 phase and eventually to a permanent cell cycle exit called senescence. One of the main features of the senescence is an increased cell size. For many years, it was believed that the non-dividing cells simply continue to grow and as a result, they become excessively large. There is now emerging evidence that the increased cell size is a cause rather than consequence of the cell cycle arrest. This review aims to summarize recent advances in our understanding of senescence induction, in particular that resulting from treatment with CDK4/6 inhibitors.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10608 - Biochemistry and molecular biology
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2023
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Folia Biologica
ISSN
0015-5500
e-ISSN
0015-5500
Svazek periodika
69
Číslo periodika v rámci svazku
5-6
Stát vydavatele periodika
CZ - Česká republika
Počet stran výsledku
3
Strana od-do
194-196
Kód UT WoS článku
001199526300003
EID výsledku v databázi Scopus
2-s2.0-85190398748