Molecular Cancer Therapeutics
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Mol Cancer Ther. 2006;5:2444-2449
© 2006 American Association for Cancer Research

Reviews

Developing gene expression signatures of pathway deregulation in tumors

James W. Watters1 and Christopher J. Roberts2

1 Department of Molecular Profiling, Merck Research Laboratories, West Point, Pennsylvania and 2 Rosetta Inpharmatics LLC (a wholly owned subsidiary of Merck & Co., Inc.), Seattle, Washington

Requests for reprints: Christopher J. Roberts, Rosetta Inpharmatics LLC, 401 Terry Avenue North, Seattle, WA 98109. Phone: 206-802-7304. E-mail: christopher_roberts2{at}merck.com

Recent advances in our understanding of cancer biology have led to the development of therapies targeting specific signaling pathways. Molecular targeting promises to improve our ability to predict who will respond by assessing the state of these targeted pathways in patients. However, a single pathway can be deregulated by multiple mechanisms, and for some pathways it may be difficult to assess activation state by analyzing a single oncogene or tumor suppressor. Therefore, developing gene expression signatures of pathway activation status using model systems or human tumor samples may enable a more reliable measurement of pathway activity. This review discusses recent advances in the identification of gene expression–based signatures of pathway deregulation and how this information may lead to improved therapeutic response prediction. [Mol Cancer Ther 2006;5(10):2444–9]


Received 6/ 8/06; revised 7/31/06; accepted 8/25/06.







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
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2006 by the American Association for Cancer Research.