» Articles » PMID: 31292714

Models Used to Screen for the Treatment of Multidrug Resistant Cancer Facilitated by Transporter-based Efflux

Overview
Specialty Oncology
Date 2019 Jul 12
PMID 31292714
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Efflux transporters of the adenosine triphosphate-binding cassette (ABC)-superfamily play an important role in the development of multidrug resistance (multidrug resistant; MDR) in cancer. The overexpression of these transporters can directly contribute to the failure of chemotherapeutic drugs. Several in vitro and in vivo models exist to screen for the efficacy of chemotherapeutic drugs against MDR cancer, specifically facilitated by efflux transporters.

Results: This article reviews a range of efflux transporter-based MDR models used to test the efficacy of compounds to overcome MDR in cancer. These models are classified as either in vitro or in vivo and are further categorised as the most basic, conventional models or more complex and advanced systems. Each model's origin, advantages and limitations, as well as specific efflux transporter-based MDR applications are discussed. Accordingly, future modifications to existing models or new research approaches are suggested to develop prototypes that closely resemble the true nature of multidrug resistant cancer in the human body.

Conclusions: It is evident from this review that a combination of both in vitro and in vivo preclinical models can provide a better understanding of cancer itself, than using a single model only. However, there is still a clear lack of progression of these models from basic research to high-throughput clinical practice.

Citing Articles

Unveiling the therapeutic potential of cabozantinib-loaded poly D,L-lactic-co-glycolic acid and polysarcosine nanoparticles in inducing apoptosis and cytotoxicity in human HepG2 hepatocellular carcinoma cell lines and anti-tumor activity in SCID....

Bhattacharya S, Parihar V, Prajapati B Front Oncol. 2023; 13:1125857.

PMID: 36874145 PMC: 9975495. DOI: 10.3389/fonc.2023.1125857.


Exploring near-infrared absorbing nanocarriers to overcome cancer drug resistance.

Chu S, Stochaj U Cancer Drug Resist. 2022; 3(3):302-333.

PMID: 35582453 PMC: 8992494. DOI: 10.20517/cdr.2020.20.


Curcumin-Loaded Solid Lipid Nanoparticles Bypass P-Glycoprotein Mediated Doxorubicin Resistance in Triple Negative Breast Cancer Cells.

Fathy Abd-Ellatef G, Gazzano E, Chirio D, Hamed A, Belisario D, Zuddas C Pharmaceutics. 2020; 12(2).

PMID: 31991669 PMC: 7076516. DOI: 10.3390/pharmaceutics12020096.

References
1.
Killion J, Radinsky R, Fidler I . Orthotopic models are necessary to predict therapy of transplantable tumors in mice. Cancer Metastasis Rev. 1999; 17(3):279-84. DOI: 10.1023/a:1006140513233. View

2.
Krishna R, Mayer L . Multidrug resistance (MDR) in cancer. Mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of anticancer drugs. Eur J Pharm Sci. 2000; 11(4):265-83. DOI: 10.1016/s0928-0987(00)00114-7. View

3.
Desoize B, Jardillier J . Multicellular resistance: a paradigm for clinical resistance?. Crit Rev Oncol Hematol. 2000; 36(2-3):193-207. DOI: 10.1016/s1040-8428(00)00086-x. View

4.
Rao M, Reddy J . Histogenesis of pseudo-ductular changes induced in the pancreas of guinea pigs treated with N-methyl-N-nitrosourea. Carcinogenesis. 1980; 1(12):1027-37. DOI: 10.1093/carcin/1.12.1027. View

5.
Johnson J, Decker S, Zaharevitz D, Rubinstein L, Venditti J, SCHEPARTZ S . Relationships between drug activity in NCI preclinical in vitro and in vivo models and early clinical trials. Br J Cancer. 2001; 84(10):1424-31. PMC: 2363645. DOI: 10.1054/bjoc.2001.1796. View