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Vol. 28, Issue 8, 987-993, August 2000
Department of Pharmaceutics, State University of New York
at Buffalo, Buffalo, New York (L.T.N., M.R., K.D.); and Department of
Neurology, Buffalo General Hospital, Buffalo, New York (B.W.-G., C.M.,
M.P., K.P., C.B., L.D.J.)
The purpose of this study was to determine whether the expression
of cytochrome P450 (CYP) enzyme mRNAs, other drug-metabolizing enzyme
mRNAs, and transporter mRNAs can be detected using DNA arrays. Total
RNA was isolated from peripheral blood mononuclear cells of 10 multiple
sclerosis patients and 10 age- and sex-matched controls. The mRNA was
reverse transcribed to radiolabeled cDNA, and the resultant cDNA was
used to probe a DNA array containing several thousand known human
genes. The signals corresponding to several CYPs, drug-metabolizing,
and transporter mRNAs was substantially above background. The results
demonstrate that the DNA array technique has the sensitivity and the
selectivity for applications in the pharmaceutical sciences. The mean
values for mRNAs of specific CYPs and drug-metabolizing enzymes in
peripheral blood cells were compared with reported values for liver.
The capabilities of DNA arrays may prove useful for characterizing CYP
expression in a variety of clinical samples.
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