Extracellular Vesicles and Cancer Multidrug Resistance: Undesirable Intercellular Messengers?

被引:5
作者
Bucci-Munoz, Maria [1 ]
Gola, Aldana Magali [1 ]
Rigalli, Juan Pablo [2 ]
Ceballos, Maria Paula [1 ]
Ruiz, Maria Laura [1 ]
机构
[1] Inst Fisiol Expt CONICET, Fac Ciencias Bioquim & Farmaceut UNR, RA-2000 Rosario, Argentina
[2] Heidelberg Univ Hosp, Dept Clin Pharmacol & Pharmacoepidemiol, Neuenheimer Feld 410, D-69120 Heidelberg, Germany
来源
LIFE-BASEL | 2023年 / 13卷 / 08期
关键词
ABC transporters; drug resistance; extracellular vesicles; P-glycoprotein; breast cancer resistance protein; multidrug resistance-associated protein; P-GLYCOPROTEIN EXPRESSION; BREAST-CANCER; DRUG-RESISTANCE; ABC TRANSPORTERS; OVARIAN-CANCER; TRANSCRIPTIONAL REGULATION; DIFFERENTIAL REGULATION; INTRINSIC RESISTANCE; PROMOTER METHYLATION; RNA STABILIZATION;
D O I
10.3390/life13081633
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cancer multidrug resistance (MDR) is one of the main mechanisms contributing to therapy failure and mortality. Overexpression of drug transporters of the ABC family (ATP-binding cassette) is a major cause of MDR. Extracellular vesicles (EVs) are nanoparticles released by most cells of the organism involved in cell-cell communication. Their cargo mainly comprises, proteins, nucleic acids, and lipids, which are transferred from a donor cell to a target cell and lead to phenotypical changes. In this article, we review the scientific evidence addressing the regulation of ABC transporters by EV-mediated cell-cell communication. MDR transfer from drug-resistant to drug-sensitive cells has been identified in several tumor entities. This was attributed, in some cases, to the direct shuttle of transporter molecules or its coding mRNA between cells. Also, EV-mediated transport of regulatory proteins (e.g., transcription factors) and noncoding RNAs have been indicated to induce MDR. Conversely, the transfer of a drug-sensitive phenotype via EVs has also been reported. Additionally, interactions between non-tumor cells and the tumor cells with an impact on MDR are presented. Finally, we highlight uninvestigated aspects and possible approaches to exploiting this knowledge toward the identification of druggable processes and molecules and, ultimately, the development of novel therapeutic strategies.
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页数:33
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