Ivaska's research team is working at Turku Centre for Biotechnology, University of Turku and Åbo Academy. Large-scale screens aiming at find potential new genes regulating cancer cell metastasis revealed to the research team an unexpected link between brain development and tumor invasion. Amazingly, the ability of cancer cells to adhere and migrate on their environment and invade into surrounding tissue were prevented by SHANK protein – a molecule previously studied in the central nervous system and linked to autism, describes graduate student Johanna Lilja. In cell culture experiments, the researchers found that SHANK protein limits the ability of a protein called Rap1 to activate cell adhesion receptors, integrins. This same mechanism regulated cancer cell motility as well as the morphology and branching of neurites, known to be essential for normal brain function. To reveal the underlying mechanism the co-operation of three international research group was needed. Dr. Igor Barsukov’s laboratory from University of Liverpool solved the 3-dimensional structure of SHANK protein, which led the researchers to study the correct mechanism. Then, Ivaska’s research team in collaboration with neuroscientist Dr. Hans-Juergen Kreienkamp from Institute for Human Genetics, Hamburg, studied the function of SHANK in both cancer cells and neurons.
The research team and their collaborators are currently assessing if SHANK proteins have other impacts on cancer cells - especially on their proliferation. The findings were published in the highly appreciated Nature Cell Biology - journal on the 6th of March 2017.
Figure legend: SHANK regulates adhesion and protrusion in very different cell types: cancer cells and neurons. Image taken by Dr Guillaume Jacquemet reveals the distinct morphologies of neurons and cancer cells. On the right: Primary Rat hippocampal neuron stained for actin (green) Dapi (blue) and MAP2 (purple). On the left a bone cancer cell stained for Actin (red) and paxillin (green).