Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/28181
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Type: Journal article
Title: Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes
Author: Powell, J.
Gardner, A.
Bais, A.
Hinze, S.
Baker, E.
Whitmore, S.
Crawford, J.
Kochetkova, M.
Spendlove, H.
Doggett, N.
Sutherland, G.
Callen, D.
Kremmidiotis, G.
Citation: Genomics, 2002; 80(3):303-310
Publisher: Academic Press Inc
Issue Date: 2002
ISSN: 0888-7543
1089-8646
Statement of
Responsibility: 
Jason A. Powell, Alison E. Gardner, Anthony J. Bais, Susan J. Hinze, Elizabeth Baker, Scott Whitmore, Joanna Crawford, Marina Kochetkova, Hayley E. Spendlove, Norman A. Doggett, Grant R. Sutherland, David F. Callen, and Gabriel Kremmidiotis
Abstract: Loss of heterozygosity (LOH) of chromosome 16q24.3 is a common genetic alteration observed in invasive ductal and lobular breast carcinomas. We constructed a physical map and generated genomic DNA sequence data spanning 2.4 Mb in this region. Detailed in silico and in vitro analyses of the genomic sequence data enabled the identification of 104 genes. It was hypothesized that tumor-suppressor genes would exhibit marked mRNA expression variability in a panel of breast cancer cell lines as a result of downregulation due to mutation or hypermethylation. We examined the mRNA expression profiles of the genes identified at 16q24.3 in normal breast, a normal breast epithelial cell line, and several breast cancer cell lines exhibiting 16q24.3 LOH. Three of the genes, CYBA, Hs.7970, and CBFA2T3, exhibited variability ten times higher than the baseline. The possible role of these genes as tumor suppressors is discussed.
Keywords: Chromosomes, Human, Pair 16; Humans; Breast Neoplasms; Genetic Predisposition to Disease; Physical Chromosome Mapping; Gene Expression Profiling; Sequence Analysis, DNA; Loss of Heterozygosity; Genes, Tumor Suppressor; Female
Rights: © 2002 Elsevier Science (USA). All rights reserved.
RMID: 0020020819
DOI: 10.1006/geno.2002.6828
Appears in Collections:Paediatrics publications
Molecular and Biomedical Science publications

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