Annals of Oncology 10:455-460, 1999
© 1999 European Society for Medical Oncology
research-article |
Induction of 
-glutamylcysteine synthetase gene expression by platinum drugs in peripheral mononuclear cells of lung cancer patients
1Second Department of Internal Medicine, Hiroshima University School of Medicine
2Evaluation Division I, Pharmaceuticals and Medical Devices Evaluation Center, National Institute of Health Sciences
3Department of Environment and Mutation, Research Institute for Radiation Biology and Medicine, Hiroshima University Japan
Correspondence to. Y. Fujiwara, MD, PhD., 2nd Department of Internal Medicine, Hiroshima University School of Medicine, Kasumi 1-2-3, Minami-ku, Hiroshima, 734-8551, Japan E-mail: fujiwara{at}nihs.go.jp
Background: To investigate in vivo the roles of 
-glutamylcysteine synthetase (y-GCS), multidrug resistance-associated protein (MRP), human canalicular multispecific organic anion transporter (cMOAT) and DNA topoisomerase I (topo I) in relation to platinum drug resistance, we monitored the changes of the steady-state levels of the mRNAs for these factors in peripheral mononuclear cells (PMN) after completing platinum drug administration.
Patients and methods PMN from 46 subjects were studied. We obtained PMN from 14 previously untreated lung cancer patients and 14 normal volunteers to measure the baseline gene expression levels. We then obtained PMN from 18 patients with previously untreated advanced lung cancer before and after they received platinum drug treatment. We analyzed the gene expression levels by using the quantitative reverse transcription polymerase chain reaction (RT-PCR).
Results: There were no differences in the baseline expression levels between normal volunteers and lung cancer patients in any of the genes. After platinum drug administration, the heavy subunit of -GCS (-GCSh) expression level increased 2.5-fold within 24 hours and the increase persisted for a month, whereas the light subunit of -GCS (-GCSl) expression level did not show an early response but had increased after a month. By contrast, the MRP, cMOAT and topo I expression levels were similar before, during and after chemotherapy.
Conclusions: These results suggest that the gene expression levels of both subunits of -GCS play an important in vivo role in platinum drug resistance.
cMOAT, -GCS heavy subunit, -GCS light sub-unit, MRP, platinum drug resistance
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