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Silencing of Cited2 and Akap12 genes in radiation-induced rat osteosarcomas
- Source :
- Biochemical and Biophysical Research Communications. 390:654-658
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- We have previously studied genomic copy number changes and global gene expression patterns in rat osteosarcomas (OS) induced by the bone-seeking alpha emitter (238)Pu by comparative genomic hybridization (CGH) and oligonucleotide microarray analyses, respectively. Among the previously identified genes that were down-regulated in radiation-induced rat OS tumors, Cited2 (Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2) and Akap12 (a kinase anchoring protein, also known as src-suppressed C-kinase substrate, SSeCKS) genes mapped to the most frequently lost regions on chromosome 1p. In the present study, relative copy number losses of Cited2 and Akap12 genes were observed in 8 of 15 (53%) and 10 of 15 (67%) tumors by quantitative PCR analysis. Loss of Cited2 and Akap12 in the tumors was confirmed at the levels of mRNA and protein expression by quantitative RT-PCR and immunoblot analyses, respectively. These results indicate that Cited2 and Akap12 are silenced in radiation-induced OS, and therefore are novel candidate tumor-suppressor genes of this tumor.
- Subjects :
- Neoplasms, Radiation-Induced
Tumor suppressor gene
Gene Dosage
Biophysics
A Kinase Anchor Proteins
Bone Neoplasms
Cell Cycle Proteins
Biology
Biochemistry
Gene dosage
Rats, Sprague-Dawley
Gene duplication
Gene expression
Animals
Genes, Tumor Suppressor
Gene Silencing
Molecular Biology
Gene
Regulation of gene expression
Osteosarcoma
Cell Biology
Molecular biology
Rats
Gene Expression Regulation, Neoplastic
Gene chip analysis
Female
Transcription Factors
Comparative genomic hybridization
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 390
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....9b099725621a3f871eff920dc82452d5
- Full Text :
- https://doi.org/10.1016/j.bbrc.2009.10.022