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Updated: Aug 17, 2026

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
[Multidrug resistance: diagnostic approaches and difficulties]
Orsolya Rideg1, Péter Csutora, Tamás Magyarlaki
1Pécsi Tudományegyetem, Altalános Orvostudományi Kar, Laboratóriumi Medicina Intézet, Pécs.
Abstract:
During the mid sixties scientists recognized that tumour cells can be resistant to a variety of chemotherapeutical drugs of different chemical structure simultaneously. They named this phenomenon multidrug resistance (MDR). Following this observation, number of in vitro and in vivo experiments proved that transmembrane proteins of the cell membrane are responsible for the mechanism. Many details of the underlying biochemical mechanisms were explored during the past decade. Nowadays the importance of MDR is well appreciated in different walks of medical science. MDR is an important problem during the treatment of many haematological conditions and solid organ tumors. Also, MDR is an important factor during immunosuppressant therapy of the transplanted patients. In spite of extensive research there are many uncertainties around MDR. This brief review describes the present options in the investigation of MDR. Based upon the MDR genotyping and expression level the likelihood of drug resistance may be predicted with reasonable accuracy. Additional information may be obtained by measuring the P-glycoprotein expression on the cell surface and the outward transport of test molecules from the cells. Although the tests described above provide significant help in predicting MDR or in the confirmation of existing MDR there is no consensus about the laboratory diagnosis.
Insights
Multidrug resistance (MDR) in cancer and transplant patients poses a significant challenge. Investigating MDR through genotyping and protein expression can help predict drug resistance, though diagnostic consensus is lacking.
Area of Science:
- Oncology
- Pharmacology
- Immunology
Background:
- Multidrug resistance (MDR) was recognized in the 1960s as simultaneous resistance of tumor cells to various chemotherapeutics.
- Transmembrane proteins are key mediators of MDR, with biochemical mechanisms extensively studied.
- MDR is a critical issue in treating hematological and solid organ tumors, and in immunosuppressive therapy for transplant recipients.
Purpose of the Study:
- To review current methods for investigating multidrug resistance (MDR).
- To highlight the importance of MDR in various medical fields.
Main Methods:
- Analysis of MDR genotyping and expression levels.
- Measurement of P-glycoprotein expression on cell surfaces.
- Assessment of outward transport of test molecules from cells.
Main Results:
- MDR genotyping and expression levels can predict drug resistance with reasonable accuracy.
- P-glycoprotein levels and molecule transport provide additional insights into MDR.
- Current testing methods aid in predicting or confirming MDR.
Conclusions:
- Despite advancements, uncertainties remain regarding MDR.
- Predictive testing for MDR shows promise but lacks standardized laboratory diagnostic consensus.
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