Cancer Research Donn Young  Jordan
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

[Cancer Research 54, 1393-1396, March 15, 1994]
© 1994 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schott, D. R.
Right arrow Articles by Smith, H. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schott, D. R.
Right arrow Articles by Smith, H. S.

A Candidate Tumor Suppressor Gene in Human Breast Cancers1

David R. Schott2, Julielani Ngo Chang2, Guoren Deng, Wayne Kurisu, Wen-Lin Kuo, Joe Gray and Helene S. Smith3

Geraldine Brush Cancer Research Institute, California Pacific Medical Center, San Francisco, California 94115-1932 [D. R. S., G. D., W. K., H. S. S.]; The Jules Stein Eye Institute and Department of Ophthalmology, University of California at Los Angeles, Los Angeles, California 90024 [J. N. C.]; and Division of Molecular Cytometry, Department of Laboratory Medicine, University of California, San Francisco, California 94143 [W-L. K., J. G.]

We have isolated a candidate gene (designated Brush-1) located at 13q12–q13, proximal to the retinoblastoma gene (RB1). Brush-1 codes for a 4.7-kilobase mRNA expressed at high levels in normal breast epithelium but drastically reduced in 6 of 13 breast cancer cell lines. RB1 mRNA expression is at normal levels for 5 of these 6 lines suggesting a greater importance of Brush-1 for breast cancer. Four primary breast tumors which showed no loss of heterozygosity in the 13q13–q14 region demonstrated normal levels of mRNA for both Brush-1 and RB1. However, four additional primary tumors which displayed loss of heterozygosity for this region had markedly decreased levels of Brush-1 mRNA while maintaining the normal levels for RB1. This differential loss of Brush-1 mRNA expression for both primary tumors and breast cancer cell lines is the expected pattern for a breast tumor suppressor gene.

1 Supported by Grant P01 CA44768 from the NIH.

2 Additionally supported by fellowships from the Fenton Family Foundation and the Susan G. Komen Foundation.

3 To whom requests for reprints should be addressed, at Geraldine Brush Cancer Research Institute, California Pacific Medical Center, 2330 Clay Street, San Francisco, CA 94115.

Received 12/ 9/93. Accepted 2/ 4/94.




This article has been cited by other articles:


Home page
Arch Otolaryngol Head Neck SurgHome page
T. J. Belbin, B. Singh, R. V. Smith, N. D. Socci, V. B. Wreesmann, M. Sanchez-Carbayo, J. Masterson, S. Patel, C. Cordon-Cardo, M. B. Prystowsky, et al.
Molecular Profiling of Tumor Progression in Head and Neck Cancer
Arch Otolaryngol Head Neck Surg, January 1, 2005; 131(1): 10 - 18.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
L. A. Scott, J. K. Vass, E. K. Parkinson, D. A. F. Gillespie, J. N. Winnie, and B. W. Ozanne
Invasion of Normal Human Fibroblasts Induced by v-Fos Is Independent of Proliferation, Immortalization, and the Tumor Suppressors p16INK4a and p53
Mol. Cell. Biol., February 15, 2004; 24(4): 1540 - 1559.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
M. Esteller, J. M. Silva, G. Dominguez, F. Bonilla, X. Matias-Guiu, E. Lerma, E. Bussaglia, J. Prat, I. C. Harkes, E. A. Repasky, et al.
Promoter Hypermethylation and BRCA1 Inactivation in Sporadic Breast and Ovarian Tumors
J Natl Cancer Inst, April 5, 2000; 92(7): 564 - 569.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
D. J. Simpson, J. Magnay, J. E. Bicknell, A. L. Barkan, A. M. McNicol, R. N. Clayton, and W. E. Farrell
Chromosome 13q Deletion Mapping in Pituitary Tumors: Infrequent Loss of the Retinoblastoma Susceptibility Gene (RB1) Locus Despite Loss of RB1 Protein Product in Somatotrophinomas
Cancer Res., April 1, 1999; 59(7): 1562 - 1566.
[Abstract] [Full Text] [PDF]




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 © 1994 by the American Association for Cancer Research.