2021
Tumour Microenvironment Stress Promotes the Development of Drug Resistance
SEEBACHER, Nicole A., Mária KRCHNIAKOVÁ, Alexandra E. STACY, Jan ŠKODA, Patric J. JANSSON et. al.Základní údaje
Originální název
Tumour Microenvironment Stress Promotes the Development of Drug Resistance
Autoři
SEEBACHER, Nicole A., Mária KRCHNIAKOVÁ (703 Slovensko, domácí), Alexandra E. STACY, Jan ŠKODA (203 Česká republika, domácí) a Patric J. JANSSON
Vydání
Antioxidants, Basel, MDPI, 2021, 2076-3921
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10601 Cell biology
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 7.675
Kód RIV
RIV/00216224:14310/21:00119405
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000724516000001
Klíčová slova anglicky
tumour microenvironmental stress; drug resistance; reactive oxygen species; cancer stem cells
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 9. 12. 2021 14:41, Mgr. Marie Šípková, DiS.
Anotace
V originále
Multi-drug resistance (MDR) is a leading cause of cancer-related death, and it continues to be a major barrier to cancer treatment. The tumour microenvironment (TME) has proven to play an essential role in not only cancer progression and metastasis, but also the development of resistance to chemotherapy. Despite the significant advances in the efficacy of anti-cancer therapies, the development of drug resistance remains a major impediment to therapeutic success. This review highlights the interplay between various factors within the TME that collectively initiate or propagate MDR. The key TME-mediated mechanisms of MDR regulation that will be discussed herein include (1) altered metabolic processing and the reactive oxygen species (ROS)-hypoxia inducible factor (HIF) axis; (2) changes in stromal cells; (3) increased cancer cell survival via autophagy and failure of apoptosis; (4) altered drug delivery, uptake, or efflux and (5) the induction of a cancer stem cell (CSC) phenotype. The review also discusses thought-provoking ideas that may assist in overcoming the TME-induced MDR. We conclude that stressors from the TME and exposure to chemotherapeutic agents are strongly linked to the development of MDR in cancer cells. Therefore, there remains a vast area for potential research to further elicit the interplay between factors existing both within and outside the TME. Elucidating the mechanisms within this network is essential for developing new therapeutic strategies that are less prone to failure due to the development of resistance in cancer cells.
Návaznosti
GJ20-00987Y, projekt VaV |
|