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[Cancer Research 57, 152-155, January 1, 1997]
© 1997 American Association for Cancer Research

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Glutathione Metabolism in Patients with Non-Small Cell Lung Cancers

Sarah L. Blair, Paul Heerdt, Sonu Sachar, Amir Abolhoda, Steven Hochwald, Huiming Cheng and Michael Burt1

Department of Surgery, Memorial Sloan-Kettering Cancer Center New York, NY 10021 [S. L. B., S. S., A. A., S. H., H. C., M. B.], and Department of Anesthesiology and Critical Care Medicine, Memorial Sloan-Kettering Cancer Center, Department of Anesthesiology, New York Hospital, Cornell Medical Center, New York, NY 10021 [P. H.]

Non-small cell lung cancer (NSCLC) is the leading cause of cancer death in the United States. Because NSCLC is highly chemoresistant, it is usually not treatable. Altered glutathione (GSH) metabolism is thought to be one major mechanism of chemoresistance, and GSH levels are reported to be elevated in NSCLC. The main objective of this study is to delineate the potential mechanisms involved in elevation of tissue GSH, including extraction from the circulation by NSCLC. Twenty consecutive patients with NSCLC were enrolled. At the time of lobectomy, pulmonary artery and vein were identified, and blood flow was measured by an electromagnetic probe. Subsequently, blood samples were drawn from pulmonary artery, the vein draining the tumor-bearing lobe, and a normal lobe. Immediately after lobectomy, tumor and lung specimens were snap frozen. NSCLC tumor specimens had higher levels of GSH compared with lung tissue (20.8 ± 9.4 versus 11.6 ± 3.0 nmol/mg protein, respectively; P < 0.05). The tumor demonstrated higher activity of the enzyme {gamma}-glutamyl transpeptidase, a membrane-bound enzyme involved in transmembrane uptake of GSH, than lung tissue (41.9 ± 26.4 versus 22.4 ± 12.3 units/mg protein, respectivel; P < 0.05). Also, the tumor-bearing lobe showed elevated extraction of GSH and two of its component amino acids compared with lung tissue (GSH uptake: 0.60 ± 0.67 versus 0.20 ± 0.40 µM/min, respectively; P < 0.05). NSCLC tumors are able to extract circulating GSH and its constituent amino acids to synthesize intracellular GSH. Increased activity of {gamma}-glutamyl transpeptidase may be one mechanism underlying increased GSH uptake by NSCLC.

1 To whom requests for reprints should be addressed, at Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021. Phone: (212) 639-8026; Fax: (212) 717-3124.

Received 6/20/96. Accepted 10/31/96.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1997 by the American Association for Cancer Research.