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. Author manuscript; available in PMC: 2017 Jun 2.
Published in final edited form as: J Clin Oncol. 2004 Mar 15;22(6):1078–1086. doi: 10.1200/JCO.2004.07.048

Table 4.

Summary of Multidrug Resistance Data

Features MDR+ (n = 63)* MDR− (n = 28)
Shift
 Median 62 24
 Range 10–99 1–98

PSC§
 Median 86 16
 Range 40–100 0–31

Cyclosporine§
 Median 88 8
 Range 17–100 0–33

MRK-16
 Median 65 18
 Range 2–99 1–97

KS/D
 Median 0.74 0.40
 Range 0.07–9.8 0.05–9.5

MESF#
 Median 6,312 3,580**
 Range 1,625–20,007 491–12,612

Abbreviations: MDR, multidrug resistance; PSC, valspodar; KS/D, Kolmogorov-Smirnov Statistics; MESF, molecules of equivalent soluble fluorochrome; P-gp, P170-glycoprotein.

*

≥40% in vitro rhodamine efflux from CD34+ blast cells (see Methods).

Rhodamine fluorescence channel shift, reflecting cellular rhodamine efflux, from baseline (maximal dye uptake and retention) that occurred during a 1-hour incubation of cells at 37°C (to induce dye efflux), expressed as percentage of maximal dye retention.

P = .001.

§

Percentage of inhibition of in vitro rhodamine efflux from blast cells in the presence of these agents.

Percentage of blast cells immuno-stained with anti-P-gp antibody MRK-16.

Binding of MRK-16 to blast cells relative to background using Kolmogorov-Smirnov statistics, whereby the generated D value reflects the difference between the two binding curves.

#

MESF (MRK-16 immuno-staining), an indicator of P-gp protein density in the cellular membrane of blast cells.

**

P = .006.