On the other side its behaviour varies quite a lot. While some GIST tumours are relatively harmless, others may become metastatic. For some time now such tumours can be treated in targeted therapies. But since such treatments are not effective for all GIST tumours there is a lot of interest in alternative treatments.
A research team led by Peter Birner from the Clinical Institute of Pathology at the MedUni Vienna has now identified the enzyme MAPKAP kinase 2 as important for the progression of GIST. Birner states: “These results are interesting since we hardly knew anything about the role of MAPKAP kinase 2 in malignant cancer.“
However, it was known that this protein plays an important role in inflammatory diseases such as rheumatoid arthritis. Due to this, there are already several selective inhibitors against MAPKAP kinase 2. According to Birner these medicines could possibly be used in future therapies for GIST patients.
The discovery of this mechanism also relativises the meaning of the cancer gene ETV1 that in the case of GIST is regulated by MAPKAP kinase 2. At the end of 2010 a study claimed that ETV1 plays a central role for the origin and progression of GIST. This assumption has been partially relativised by Birner and his research team: “Our research results show that MAPKAP kinase 2 is obviously more important for the progression of GIST than ETV1, which is only upregulated in some tumours.“
Sebastian Schoppmann of the University Department of Surgery at MedUni Vienna says: “This study is very welcomed since it shows that Austria ranks among the international top countries in the research of rare tumours, without conducting large prospective studies as this is the case in the US.“
MEDICA.de; Source: Medical University of Vienna