- Paper Report
- Open Access
Amplification at 17q23 in breast cancer
- Chris Jones1
© Current Science Ltd 2000
- Published: 1 December 2000
- breast cancer
Studies using comparative genomic hybridisation (CGH) have demonstrated that chromosome 17q23 is amplified in up to 20% of primary breast tumours. This increase in DNA copy number has been shown to be due to high-level amplification of at least two distinct regions at 17q23. To further characterize this region of amplification in breast tumorigenesis, six genes localised to 17q23 in breast cancer cell lines were analysed for amplification frequency in primary breast tumours.
To assess amplification frequencies of six genes localised to 17q23 in primary breast carcinoma.
Breast cancer cell lines were analysed by Southern and northern hybridisation and FISH to determine amplification and expression of genes which mapped to 17q23. Wu et al analysed amplification by Southern hybridisation, and expression by semi-quantitative RT-PCR in 94 primary breast tumours. Barlund et alexamined amplification in 372 primary breast tumours on a tissue array by FISH, and expression in 12 tumours by LightCycler RT-PCR.
The genes PAT1, PS6K, and RAD51C were identified as being both amplified and overexpressed in the breast cancer cell lines analysed by both groups. In addition, although both groups identified SIGMA1B, Barlund et al found poor correlation between expression and amplification levels for this gene. However Barlund et al did identify TBX2 as another overexpressed and amplified gene. In primary breast tumours, PAT1 was amplified in 19% and 8.9% of cases, PS6K in 7.5% and 10.2%, and RAD51C in 8% and 3.1% in the Wu et al and Barlund et al studies, respectively. SIGMA1 was amplified in 12% and TBX2in 8.6% of cases in the appropriate study. For each gene, there were instances of amplification without overexpression, and/or vice versa.
Both groups have identified genes localised to the chromosome 17q23 amplicon which are amplified and overexpressed in breast cancer cell lines and primary tumours. Taken together, there are at least five genes at 17q23 which appear to be associated with the amplification in breast carcinomas, with potential upregulation of PAT1, PS6K, RAD51C, SIGMA1B and TBX2. PS6K is a serine-threonine kinase involved in G1 to S-phase progression, and provides an excellent candidate for an amplification target gene based on its biological role. However, the equivocal correlation between amplification and overexpression of PS6K observed in one of the studies (Wu et al) raises doubts as to its oncogenic nature. This correlation is a general feature of all genes investigated across the two studies.
Wu G-J, Sinclair CS, Paape J, Ingle JN, Roche PC, James CD and Couch FJ: 17q23 amplifications in breast cancer involve the PAT1 , RAD51C , PS6K and SIGMA1B genes. Cancer Res 2000, 60:5371-5375 (PubMed%20abstract).