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Originally published as JCO Early Release 10.1200/JCO.2006.05.9501 on August 8 2006 © 2006 American Society of Clinical Oncology. Lactate Dehydrogenase 5 Expression in Operable Colorectal Cancer: Strong Association With Survival and Activated Vascular Endothelial Growth Factor Pathway—A Report of the Tumour Angiogenesis Research Group
From the Departments of Pathology, and Radiotherapy/Oncology, Democritus University of Thrace, Alexandroupolis, Greece; Department of Pathology, Nuffield Department of Clinical Laboratory Sciences, John Radcliffe Hospital; Cancer Research UK, Molecular Oncology Laboratories, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom Address reprint requests to Michael I. Koukourakis, MD, Tumor and Angiogenesis Research Group, PO BOX 12, Alexandroupolis 68100, Greece; e-mail: targ{at}her.forthnet.gr Purpose: Lactate dehydrogenase 5 (LDH-5) regulates, under hypoxic conditions, the anaerobic transformation of pyruvate to lactate for energy acquisition. Several studies have shown that serum LDH may be an ominous prognostic marker in malignant tumors. The clinical significance of tissue LDH-5, however, remains largely unexplored.
Patients and Methods: We investigated the immunohistochemical expression of LDH-5 in a series of 128 stage II/III colorectal adenocarcinomas treated with surgery alone. In addition, markers of tumor hypoxia (hypoxia-inducible factor 1 alpha [HIF1
Results: The expression of LDH-5, together with that of HIF1 Conclusion: The immunohistochemical assessment of tissue LDH-5 and pKDR provides important prognostic information in operable colorectal cancer. The strong association between LDH-5 and pKDR expression would justify their use as surrogate markers to screen patients for tyrosin kinase inhibitor therapy. published online ahead of print at www.jco.org on August 7, 2006. Supported by the Tumour and Angiogenesis Research Group and Cancer Research UK. Terms in blue are defined in the glossary, found at the end of this article and online at www.jco.org. Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article. This article has been cited by other articles:
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Copyright © 2006 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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