Gene mutations predict sporadic breast cancer

Scientists discover gene mutations that can used for early detection of sporadic breast cancer (i.e. breast cancer for those who have no family history of the disease).

New findings from an international research group, led by Professor Jan Dumanski at Uppsala University, show that genetic alterations in apparently healthy breast cells can be associated with an increased risk for sporadic breast cancer.

‘We examined tissue samples that were located far away from the tumour and had been taken at the same time as a breast tumour had been removed. The tissues did not contain any tumour cells and looked like completely normal breast tissue. But when we analysed the DNA in these tissues we found that they contained genetic aberrations in well-known cancer genes, even though they appeared normal in the microscope’, says Jan Dumanski, Department of Immunology, Genetics and Pathology.

The study shows that the development of sporadic breast cancer is a progressive process over many years, eventually producing a tumour. The genetic aberrations in the healthy cells make up a genetic “signature” that indicates an increases risk for developing non-familial breast cancer. This knowledge can be used for future improvements in diagnostics.

‘The mutated genes create an altered protein pattern on the cells’ surface, which could be used to detect those particular cells. This opens up possibilities to develop diagnostic methods that could identify women who are at risk for developing breast cancer, before the tumour is formed and much earlier than it can be detected by e.g. mammography’, says Jan Dumanski.

The study has been published in the journal Genome Research and is the result of collaboration between research groups in Uppsala and Falun in Sweden, Krakow, Bydgoszcz and Gdansk in Poland, and Huntsville, USA.

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