Characterization of a novel metabolic strategy used by drug‐resistant tumor cells

Author:

Harper Mary‐Ellen1,Antoniou Andreas1,Villalobos‐Menuey Elizabeth2,Russo Alicia3,Trauger Richard4,Vendemelio Minda4,George Amanda3,Bartholomew Richard4,Carlo Dennis4,Shaikh Azhar1,Kupperman Jami3,Newell Evan W.5,Bespalov Ivan A.6,Wallace Susan S.7,Liu Ye4,Rogers Jeffrey R.2,Gibbs Gregory L.8,Leahy Jack L.9,Camley Robert E.3,Melamede Robert25,Newell M. Karen2

Affiliation:

1. Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine University of Ottawa Ottawa Ontario Canada

2. Department of Biology University of Colorado at Colorado Springs Colorado Springs Colorado USA

3. Department of Physics University of Colorado at Colorado Springs Colorado Springs Colorado USA

4. Division of Endocrinology, Department of Medicine University of Vermont College of Medicine Burlington Vermont USA

5. Toronto Western Research Institute and Department of Physiology University of Toronto Toronto Ontario

6. Immune Response Corporation San Diego California USA

7. Department of Microbiology and Molecular Genetics, The Markey Center for Molecular Genetics University of Vermont Burlington Vermont USA

8. Colorado Springs Colorado USA

9. Division of Immunobiology University of Vermont College of Medicine Burlington Vermont USA

Funder

National Institutes of Health

Natural Sciences and Engineering Research Council of Canada

U.S. Department of Energy

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Reference25 articles.

1. Selection for Drug Resistance Results in Resistance to Fas-Mediated Apoptosis

2. The Correlation of Membranous Glycoprotein-GP-170, Cytoplasmic Glutathione and Glucose-6-Phosphate Dehydrogenase Levels with Multidrug Resistance in Transitional Cell Carcinoma Cell Lines of the Urinary Tract

3. Cellular energy utilization and molecular origin of standard metabolic rate in mammals

4. The proton leak across the mitochondrial inner membrane

5. Role of oxidative stress generated from the mitochondrial electron transport chain and mitochondrial glutathione status in loss of mitochondrial function and activation of transcription factor nuclear factor‐kappa B: studies with isolated mitochondria and rat hepatocytes;Garcia‐Ruiz C.;Mol. Pharmacol,1995

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