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

dc.contributor.authorWillers, Clarissa
dc.contributor.authorSvitina, Hanna
dc.contributor.authorRossouw, Michael J.
dc.contributor.authorSwanepoel, Roan A.
dc.contributor.authorHamman, Josias H.
dc.contributor.authorGouws, Chrisna
dc.contributor.researchID20672322 - Willers, Clarissa
dc.contributor.researchID30884365 - Svitina, Hanna M.
dc.contributor.researchID10081097 - Hamman, Josias Hendrik
dc.contributor.researchID12450960 - Gouws, Chrisna
dc.contributor.researchID24166936 - Swanepoel, Roan Albertus
dc.contributor.researchID24093580 - Rossouw, Michael Jacques
dc.date.accessioned2019-08-07T06:27:17Z
dc.date.available2019-08-07T06:27:17Z
dc.date.issued2019
dc.description.abstractPurpose 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 practiceen_US
dc.identifier.citationWillers, C. et al. 2019. Models used to screen for the treatment of multidrug resistant cancer facilitated by transporter-based efflux. Journal of cancer research and clinical oncology, 145(8):1949-1976. [https://doi.org/10.1007/s00432-019-02973-5]en_US
dc.identifier.issn0171-5216
dc.identifier.issn1432-1335 (Online)
dc.identifier.urihttp://hdl.handle.net/10394/33106
dc.identifier.urihttps://link.springer.com/article/10.1007/s00432-019-02973-5
dc.identifier.urihttps://doi.org/10.1007/s00432-019-02973-5
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectCanceren_US
dc.subjectCell cultureen_US
dc.subjectEfflux transporteren_US
dc.subjectGenetically engineered mouse modelen_US
dc.subjectMultidrug resistanceen_US
dc.subjectPreclinical screening modelen_US
dc.titleModels used to screen for the treatment of multidrug resistant cancer facilitated by transporter-based effluxen_US
dc.typeArticleen_US

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