Models used to screen for the treatment of multidrug resistant cancer facilitated by transporter-based efflux

J Cancer Res Clin Oncol. 2019 Aug;145(8):1949-1976. doi: 10.1007/s00432-019-02973-5. Epub 2019 Jul 10.

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.

Keywords: Cancer; Cell culture; Efflux transporter; Genetically engineered mouse model; Multidrug resistance; Preclinical screening model.

Publication types

  • Review

MeSH terms

  • ATP-Binding Cassette Transporters / antagonists & inhibitors
  • ATP-Binding Cassette Transporters / genetics
  • ATP-Binding Cassette Transporters / physiology*
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology
  • Biological Transport / drug effects
  • Biological Transport / genetics
  • Culture Techniques / methods
  • Decision Support Techniques
  • Drug Resistance, Multiple* / drug effects
  • Drug Resistance, Multiple* / genetics
  • Drug Resistance, Neoplasm* / drug effects
  • Drug Resistance, Neoplasm* / genetics
  • Drug Screening Assays, Antitumor / methods*
  • Humans
  • Models, Biological*
  • Organ Specificity
  • Patient Selection

Substances

  • ATP-Binding Cassette Transporters
  • Antineoplastic Agents