2022
Noncanonical roles of p53 in cancer stemness and their implications in sarcomas
CURYLOVÁ, Lucie; Helena RAMOS; Lucília SARAIVA a Jan ŠKODAZákladní údaje
Originální název
Noncanonical roles of p53 in cancer stemness and their implications in sarcomas
Autoři
CURYLOVÁ, Lucie; Helena RAMOS; Lucília SARAIVA a Jan ŠKODA
Vydání
Cancer letters, Elsevier Ireland Ltd, 2022, 0304-3835
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 9.700
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/22:00125082
Organizační jednotka
Přírodovědecká fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
p53; Sarcoma; Mesenchymal stem cells; Cancer stem cells; p53-targeted therapy
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 6. 12. 2021 13:10, Mgr. Marie Novosadová Šípková, DiS.
Anotace
V originále
Impairment of the prominent tumor suppressor p53, well known for its canonical role as the "guardian of the genome", is found in almost half of human cancers. More recently, p53 has been suggested to be a crucial regulator of stemness, orchestrating the differentiation of embryonal and adult stem cells, suppressing reprogramming into induced pluripotent stem cells, or inhibiting cancer stemness (i.e., cancer stem cells, CSCs), which underlies the development of therapy-resistant tumors. This review addresses these noncanonical roles of p53 and their implications in sarcoma initiation and progression. Indeed, dysregulation of p53 family proteins is a common event in sarcomas and is associated with poor survival. Additionally, emerging studies have demonstrated that loss of wild-type p53 activity hinders the terminal differentiation of mesenchymal stem cells and leads to the development of aggressive sarcomas. This review summarizes recent findings on the roles of aberrant p53 in sarcoma development and stemness and further describes therapeutic approaches to restore normal p53 activity as a promising anti-CSC strategy to treat refractory sarcomas.
Návaznosti
| NU20J-07-00004, projekt VaV |
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