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[Cancer Research 64, 7201-7204, October 15, 2004]
© 2004 American Association for Cancer Research


Advances in Brief

A Gene Expression Signature Associated with Metastatic Outcome in Human Leiomyosarcomas

Yin-Fai Lee1, Megan John1, Alison Falconer1, Sandra Edwards1, Jeremy Clark1, Penny Flohr1, Toby Roe1, Rubin Wang1, Janet Shipley1, Robert J. Grimer2, D. Chas Mangham2, J. Meirion Thomas3, Cyril Fisher3, Ian Judson1 and Colin S. Cooper1

1 The Male Urological Cancer Research Centre, Institute of Cancer Research, Surrey; 2 Department of Musculoskeletal Pathology, The Royal Orthopedic Hospital National Health Service Trust, Birmingham; and 3 Department of Histopathology, The Royal Marsden National Health Service Trust, London, United Kingdom

Metastasis is a major factor associated with poor prognosis in cancer, but little is known of its molecular mechanisms. Although the clinical behavior of soft tissue sarcomas is highly variable, few reliable determinants of outcome have been identified. New markers that predict clinical outcome, in particular the ability of primary tumors to develop metastatic tumors, are urgently needed. Here, we have chosen leiomyosarcoma as a model for examining the relationship between gene expression profile and the development of metastasis in soft tissue sarcomas. Using cDNA microarray, we have identified a gene expression signature associated with metastasis in sarcoma that allowed prediction of the future development of metastases of primary tumors (Kaplan-Meier analysis P = 0.001). Our finding may aid the tailoring of therapy for individual sarcoma patients, where the aggressiveness of treatment is affected by the predicted outcome of disease.




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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 © 2004 by the American Association for Cancer Research.