INHIBITOR OF LIPID KINASE PI3KC2Α IDENTIFIED AS POTENTIAL NEW TREATMENT OF THROMBOSIS

Thrombosis including venous thrombosis and pulmonary embolism with an annual incidence of about 1 in 1,000 adults is a major threat for human health, in particular at old age. To counteract blood clotting, patients take blood thinning medication, which, however, often display severe side-effects such as bleeding (hemorrhage). The lipid kinase PI3KC2a has been found to potently modulate thrombosis by regulating the function of blood platelets that are at the heart of initiating the blood clotting mechanism e.g. in response to high blood pressure or atherosclerosis. PI3KC2a, thus, is a powerful target for the development of novel anti-thrombotic drugs. However, so far no specific inhibitor of PI3KC2a has been described.

Dr. Wen-Ting Lo from the research group of Prof. Volker Haucke in close collaboration with medicinal chemist Dr. Marc Nazaré and his team, researchers from Toulouse, and the Screening Unit of the FMP (led by Dr. Jens Peter von Kries) now has developed and characterized the first PI3KC2a inhibitors. As a result of extensive chemical optimization studies the researchers succeeded to tweak the selectivity of the inhibitors over the entire kinome, in particular against all other lipid kinases. One of these compounds termed PITCOIN3 displays particularly striking selectivity for PI3KC2a and is shown to potently impair platelet membrane remodeling and thrombus formation.

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"This breakthrough development has only been possible because of our earlier structural studies on PI3KC2a", comments Dr. Lo, the first author of the study just published in Nature Chemical Biology. Dr. Nazaré adds “that the unexpected non-classical binding mode of the PITCOIN inhibitors reveals a promising new blueprint for the development of related drug leads. The PITCOINs may also be important tools to help other researchers to probe and uncover unknown functions of PI3KC2a”.

"The antithrombotic effect of the PITCOIN inhibitors counteracts thrombosis via effects on the internal membrane structure of platelets, not by blocking their activation, thereby opening an improved therapeutic window" highlights Prof. Haucke.

The reported findings could open new possibilities for the treatment of thrombosis and cancer, as demonstrated by the ability of PITCOINs to interfere with the migration of breast cancer cells in vitro.

Source: Press release FMP

References

Lo, W.T., Belabed, H., Kücükdisli, M., Metag, J., Roske, Y., Prokofeva, P., Ohashi, Y., Horatschek, A., Cirillo, D., Krauss, M., Schmied, C., Neuenschwander, M., von Kries, J., Médard, G., Kuster, B., Perisic, O., Williams, R.L., Daumke, O., Payrastre, B., Severin, S., Nazaré, M.*, Haucke, V.* (2022) Development of selective inhibitors of phosphatidylinositol 3-kinase C2α. Nat Chem Biol, advance online publication 15 September

Li, H., Prever, L., Hsu, M.Y., Lo, W.T., Margaria, J.P., De Santis, M.C., Zanini, C., Forni, M., Novelli, F., Pece, S., Di Fiore, P.P., Porporato, P.E., Martini, M., Belabed, H., Nazare, M., Haucke, V., Gulluni, F., Hirsch, E. (2022) Phosphoinositide conversion inactivates R-Ras anddrives metastases in breast cancer. Adv. Sci. 9,e2103249. doi: 10.1002/advs.202103249. 

Contact for scientific information:

Professor Dr. Volker Haucke
NeuroCure PI
Direktor am Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)
Professor für Molekulare Pharmakologie an der Freien Universität Berlin
Mitglied des Exzellenzclusters NeuroCure
Robert-Rössle-Str.10
13125 Berlin, Campus Berlin-Buch
E-Mail: haucke@fmp-berlin.de
www.leibniz-fmp.de/haucke

Dr. Marc Nazaré
Leiter der Arbeitsgruppe Medizinische Chemie
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)Robert-Rössle-Str.10
13125 Berlin, Campus Berlin-Buch
E-Mail: nazare@fmp-berlin.de
www.leibniz-fmp.de/nazare