Testing for tumor drug resistance in the age of molecular medicine. A contribution to the Debate Round-Table on phenotypic and genotypic analyses of multidrug resistance (MDR) in clinical hospital practice

Authors
Citation
T. Efferth, Testing for tumor drug resistance in the age of molecular medicine. A contribution to the Debate Round-Table on phenotypic and genotypic analyses of multidrug resistance (MDR) in clinical hospital practice, LEUKEMIA, 13(10), 1999, pp. 1627-1629
Citations number
26
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
LEUKEMIA
ISSN journal
08876924 → ACNP
Volume
13
Issue
10
Year of publication
1999
Pages
1627 - 1629
Database
ISI
SICI code
0887-6924(199910)13:10<1627:TFTDRI>2.0.ZU;2-Q
Abstract
The detection of multidrug resistance (MDR) in clinical hospital practice r epresents an important strategy to combat clinical tumor drug resistance. P redicting the response of tumors to cytostatic drugs is of prognostic value . The 'Debate Round-Table on Phenotypic and Genotypic Analyses of Multidrug Resistance (MDR) in Clinical Hospital Practice' was launched in 1997 to ad dress specific questions on this topic. The results published thus far are a rich source to learn about the promises and pitfalls of methods, eg surro gate and functional tests and protein or mRNA expression assays as well. In the present paper, some requirements are discussed for applications of dru g resistance testing in clinical routine diagnostics. To improve the detect ion of low-level resistance, established methodologies may be strengthened with respect to: (1) standardization of sample handling, antibodies, PCR pr imers, and detection reagents; (2) standardization of protocols and far rea ching automation in performance and evaluation of results to ensure high qu ality control criteria. Sophisticated new techniques will feature: (1) high -throughput analyses for the 'horizontal screening' of single drug resistan ce genes in large numbers of patient samples at economically fair costs; (2 ) 'vertical screening' of a large number of resistance mechanisms operating upstream or downstream of the actual drug-target interaction sites, in ord er to detect more complex and multifaceted genotypes and phenotypes of mult idrug resistance.