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From the Department of Neurology, Washington University School of Medicine, St. Louis, MO (S.S.H., E.I.S., H.B.Z., D.H.G.); and the Department of Pathology, MD Anderson Cancer Center, Houston, TX (G.N.F.).
Address correspondence and reprint requests to Dr. David H. Gutmann, Department of Neurology, Washington University School of Medicine, Box 8111; 660 S. Euclid Avenue, St. Louis, MO 63110; e-mail: gutmannd{at}wustl.edu
Tumor suppressor in lung cancer-1 (TSLC1) loss is common in many human cancers, including meningioma. In this study, we demonstrate that TSLC1 protein and RNA expression is lost in 60% to 65% of high-grade gliomas, and that TSLC1 reintroduction into glioma cells results in growth suppression. Moreover, Tslc1 loss in mice results in increased astrocyte proliferation in vivo and in vitro. These data indicate that TSLC1 functions as a glioma tumor suppressor.
Supported in part from grants from the James F. McDonnell Foundation and the Department of Defense (DAMD-17-04-0266 to D.H.G.). S.S.H. is supported by a nested postdoctoral fellowship from the Department of Defense. The Siteman Cancer Center is supported in part by NCI Cancer Center Support Grant #P30 CA91842.
Disclosure: The authors report no conflicts of interest.
Received May 12, 2006. Accepted in final form July 28, 2006.
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