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[Cancer Research 62, 3587-3591, July 1, 2002]
© 2002 American Association for Cancer Research


Advances in Brief

TBX2 Is Preferentially Amplified in BRCA1- and BRCA2-related Breast Tumors1

Colleen S. Sinclair2, Camilo Adem2, Ali Naderi, Cheryl L. Soderberg, Michele Johnson, Linda Wadum, Vicki L. Couch, Thomas A. Sellers, Daniel Schaid, Jeffrey Slezak, Zach Fredericksen, James N. Ingle, Lynn Hartmann, Robert B. Jenkins and Fergus J. Couch3

Departments of Laboratory Medicine and Pathology [C. S. S., C. A., C. L. S., M. J., L. W., V. L. C., R. B. J., F. J. C.], Epidemiology [T. A. S.], Biostatistics [D. S., J. S., Z. F.], Oncology [A. N., J. N. I., L. H.], and Biochemistry and Molecular Biology [R. B. J., F. J. C.], Mayo Clinic and Foundation, Rochester, Minnesota 55905

The chromosome 17q23 region is frequently amplified in breast tumors. Gain of the region is present in 50% of BRCA1-associated breast tumors and 87% of BRCA2-associated breast tumors. The amplification frequency of the RPS6KB1 and TBX2 oncogenes from this amplicon was compared in 27 BRCA1 and BRCA2 mutant breast tumors, 15 breast tumors from high-risk patients with no BRCA1 or BRCA2 mutations, and 62 matched sporadic breast tumor controls. TBX2 was determined to be preferentially amplified and overexpressed in BRCA1 and BRCA2 mutant tumors, whereas RPS6KB1 was not, suggesting a role for TBX2 amplification in the development of BRCA1- and BRCA2-associated breast tumors.




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Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 2002 by the American Association for Cancer Research.