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Home NEWS Bioengineering

Proteomics can improve breast cancer treatment

Bioengineer by Bioengineer
September 19, 2013
in Bioengineering
Reading Time: 2 mins read
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Researchers at Karolinska Institutet in Sweden have identified a protein that could help physicians decide what type of therapy patients with hormone driven breast cancer should go through. In a study, published in Nature Communications, they show that high levels of a protein called retinoic acid receptor alpha (RARA) in breast tumors can be linked to an insufficient response to the cancer drug tamoxifen. The findings are based on a novel proteomics technique, developed at the Science for Life Laboratory.

About 80% of all breast cancer tumors depend on the female hormone estrogen to grow. Estrogen acts by binding to so-called estrogen receptors (ER) in cancer cell. Substances that block the action of estrogen have been shown to prevent the growth of many of these tumors. The goal after surgery is to prevent the growth of any cancer cell that might still be in the body after surgery. A common drug used for this purpose is tamoxifen, which blocks the action of estrogen in the breast tissue by binding to the ER of breast cells.

“This drug has been shown to be very effective, however about one third of the patients do not respond to treatment and their breast tumors return”, says Dr. Henrik Johansson, first author of the Nature Communications publication. “In our study, we show that in these cases the breast tumors often contain high amounts of RARA, which indicates that this protein has an important role in hormone driven breast cancer.”

Under the management of Associate Professor Janne Lehtiö, the research team behind the current study has put a lot of effort into studying resistance mechanism in breast cancer. This time researchers aimed to find markers that separate the groups of patients that will benefit from tamoxifen treatment from those that do not. Amongst other things, they studied protein quantities in breast cancer cell lines and made a comparison between cell lines resistant and sensitive to tamoxifen, respectively.

“In our laboratory we have developed a method that improves protein detection, which makes it possible to detect small differences in protein levels for a large number of proteins in tumor cells”, says Dr. Janne Lehtiö. “With this method we found many interesting proteins, of which one is RARA.”

The team continued to investigate RARA in two independent groups of breast cancer patients. The results show that patients with breast cancer tumors containing high levels of RARA had an increased risk of tumor recurrence, compared to patients with low levels of the protein.

“The relationship between RARA and ER is complex, and something we will continue to investigate”, says Janne Lehtiö. “However, we believe that we have identified a way to tailor breast cancer treatment to fit the individual patient, and that there also are other possibilities for technology development, which may benefit public health care in the future.”

The technique used in this project, so-called quantitative mass spectrometry-based proteomics, has been developed by the researchers in collaboration with the Swedish pharmaceutical company GE Healthcare. Janne Lehtiö’s research group is based at the Department of Oncology-Pathology at Karolinska Institutet as well as at the Swedish national research facility Science for Life Laboratory. Researchers from Sahlgrenska Academy in Gothenburg, Linköping University and Karolinska University Hospital, Solna in Stockholm County also took part in the study. The Swedish Research Council, the European Unions seventh frame program and the Swedish Cancer Society, amongst other bodies, funded the research.

Story Source:
The above story is reprinted from materials provided by Karolinska Institutet, Sabina Bossi.

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