Pregled bibliografske jedinice broj: 1020010
The multi-factorial nature of clinical multidrug resistance in cancer
The multi-factorial nature of clinical multidrug resistance in cancer // Drug resistance updates, 46 (2019), 100645, 78 doi:10.1016/j.drup.2019.100645 (međunarodna recenzija, pregledni rad, znanstveni)
CROSBI ID: 1020010 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The multi-factorial nature of clinical multidrug resistance in cancer
Autori
Assaraf, Yehuda G. ; Brozović, Anamaria ; Gonçalves, Ana Cristina ; Jurkovicova , Dana ; Linē, Aija ; Machuqueiro, Migueli ; Saponara, Simona ; Sarmento-Ribeiro, Ana Bela ; Xavier, Cristina P. R. ; Vasconcelos, M. Helena
Izvornik
Drug resistance updates (1368-7646) 46
(2019);
100645, 78
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pregledni rad, znanstveni
Ključne riječi
cancer ; clinical multidrug resistance ; cancer patients ; genetic variants ; drug-drug interactions ; drug efflux ; drug compartmentalization ; extracellular vesicles ; cell death mechanisms ; DNA damage response and repair ; epigenetic ; microRNAs ; intratumor heterogeneity and dynamics ; stem cell plasticity ; tumor microenvironment ; selection pressures ; acidic environment ; precision medicine.
Sažetak
Curative cancer therapy remains a major challenge particularly in cancers displaying multidrug resistance (MDR). The MDR phenotype is characterized by cross-resistance to a wide array of anticancer drugs harboring distinct structures and mechanisms of action. The multiple factors involved in mediating MDR may include host factors, tumor factors as well as tumor-host interactions. Among the host factors are genetic variants and drug-drug interactions. The plethora of tumor factors involves decreased diminished drug uptake primarily via impaired influx transporters, increased drug efflux predominantly due to the overexpression of multidrug efflux transporters of the ATP-binding cassette superfamily or due to drug efflux mediated by extracellular vesicles or drug-loaded lysosomes undergoing exocytosis, drug metabolism, deregulation of cell death mechanisms (i.e. anti-apoptotic modalities), enhanced DNA damage repair, epigenetic alterations and/or deregulation in microRNAs. The intratumor heterogeneity and dynamics, along with cancer stem cell plasticity, are important tumor factors. Among the tumor-host interactions are the role of the tumor microenvironment, selection pressures of various stressor conditions and agents, acidic pH and the intracellular transfer of traits mediated by extracellular vesicles. The involvement of these diverse factors in MDR highlights the need for precision medicine and real-time personalized treatments of individual cancer patients. In this review, written by a group of researchers from COST Action STRATAGEM “New diagnostic and therapeutic tools against multidrug resistant tumors”, we aim to bring together these multidisciplinary and interdisciplinary features of MDR cancers. Importantly, it is becoming increasingly clear that deciphering the molecular mechanisms underlying anticancer drug resistance, will pave the way towards the development of novel precision medicine treatment modalities that are able to surmount distinct mechanisms of anticancer drug resistance.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
COST Action 17104 STRATAGEM
HRZZ-IP-2016-06-1036 - Određivanje ključnih molekula epitelno-mezenhimalne tranzicije kao mogućih ciljeva za terapiju raka jajnika (DEvOuT) (Brozović, Anamaria, HRZZ - 2016-06) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Anamaria Brozović
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE