CURYLOVÁ, Lucie, Helena RAMOS, Lucília SARAIVA and Jan ŠKODA. Noncanonical roles of p53 in cancer stemness and their implications in sarcomas. Cancer letters. Elsevier Ireland Ltd, 2022, vol. 525, January, p. 131-145. ISSN 0304-3835. Available from: https://dx.doi.org/10.1016/j.canlet.2021.10.037.
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Basic information
Original name Noncanonical roles of p53 in cancer stemness and their implications in sarcomas
Authors CURYLOVÁ, Lucie (203 Czech Republic, belonging to the institution), Helena RAMOS, Lucília SARAIVA and Jan ŠKODA (203 Czech Republic, guarantor, belonging to the institution).
Edition Cancer letters, Elsevier Ireland Ltd, 2022, 0304-3835.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 9.700
RIV identification code RIV/00216224:14310/22:00125082
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1016/j.canlet.2021.10.037
UT WoS 000720470900007
Keywords in English p53; Sarcoma; Mesenchymal stem cells; Cancer stem cells; p53-targeted therapy
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 6/12/2021 13:10.
Abstract
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.
Links
NU20J-07-00004, research and development projectName: Faktory kmenovosti a proteiny rodiny p53 u sarkomů dětského věku: Dysregulovaná transkripční síť jako potenciální cíl terapie
Investor: Ministry of Health of the CR, Stemness factors and the p53 family proteins in pediatric sarcomas: A dysregulated transcriptional network as a potential therapeutic target, Subprogram 2 - junior
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