Research into active substances that act on the body in a personalized and targeted manner is gathering pace. An interdisciplinary team led by Bernhard Küster, Professor of Proteomics and Bioanalytics at the Technical University of Munich (TUM), has now made a decisive advance in the characterization of these active substances.
By developing a new technology, the team of natural scientists and physicians has succeeded in breaking down the interactions of active substances with hundreds of molecular processes in body cells with dose accuracy. To do this, the team uses a method that is capable of simultaneously determining thousands of proteins and their pathological modifications in a biological system and directly measuring the effect of drugs on them. The studies showed that many cancer drugs have a broader spectrum of activity than previously known. The new technology thus creates a kind of fingerprint for each active ingredient.
"Each tumor disease also has its own fingerprint of altered protein levels or activities, so even cancers that are identical by name are often individually different at the molecular level," Küster explains. "Now the challenge is to precisely analyze the fingerprints of the approximately 200 cancer drugs on the market in order to estimate their effect on the individual molecular tumor signature," says Dr. Jana Zecha, who was involved in developing the technology. This would allow existing cancer drugs to be reused in other forms of cancer via a previously undiscovered spectrum of activity. The new technology will significantly improve the search for such a "perfect match" and set a new standard in drug discovery. The technology is currently being tested in molecular tumor boards with the aim of recommending the perfect cancer therapy for each individual patient.
Publication:
https://www.science.org/doi/10.1126/science.ade3925
Scientific Contact:
Prof. Bernhard Küster
Chair of Proteomics and Bioanalytics
kuster(at)tum.de
Editing:
Susanne Neumann
TUM School of Life Sciences
Press and Public Relations