The most effective targeted cancer therapies use medications which block enzymes belonging to the kinase family. In a new study a research team from the German Cancer Consortium (DKTK) at the Technical University of Munich have examined 243 kinase inhibitors which are either approved drugs or have been tested in clinical trials. According to results published in Science, some of these may have more applications than previously thought.
In the German Cancer Consortium (DKTK), the German Cancer Research Center (DKFZ) in Heidelberg joins up with certified German university hospitals specialized in oncology.
Targeted therapy has revolutionized the treatment of certain types of cancer. An important class of drugs are kinase inhibitors, which are particularly successful in treating certain types of blood and lung cancer. Kinases are key enzymes which control a number of cell functions, such as their growth or their self-destruction. About 500 different kinases are encoded in the human genome. In cancer cells, these enzymes are often overactive and the normal regulation mechanisms cease to function. Abnormal cells can multiply uncontrollably and the growing tumor initiates the formation of blood vessels in order to sustain itself.
The international team of scientists, physicians, and computer scientists took a unique approach in order to elucidate which kinases and cellular signaling pathways are specifically targeted by the inhibitors: In over more than 6,000 hours of mass spectrometry, the researchers analyzed the interaction of 243 clinically tested inhibitors with hundreds of kinases. The activity of the inhibitors was examined under near physiological conditions. Instead of testing them using genetically produced enzymes, the scientists analyzed the entire cell content of leukemia, brain tumor, and colon cancer cells in response to the inhibitors. "In that way, we are much closer to the tumor biology and can systematically map out the spectrum of molecular binding partners."
In this "map" of the entirety of human kinases and their inhibitors, the scientists discovered new target structures which had previously not been linked to the drugs. Among them was the kinase MELK, which has been identified as a biomarker for poor prognosis in certain types of lung cancer. "Surprisingly, some of the tested inhibitors are capable of blocking MELK activity," explains Bernhard Küster. The research team also identified the precise molecular structure of several MELK-inhibitor complexes, forming the basis for the development of optimized MELK inhibitors.
The researchers discovered a new use for the kinase inhibitor cabozantinib, which is currently used to treat thyroid cancer. The results showed that cabozantinib is also effective against a kinase which plays a role in the onset of acute myeloid leukemia (AML). The drug was able to drastically slow the growth of leukemia cells in mice. "Since the agent is already an approved drug, we can take it straight to a new clinical trial," said Bernhard Küster.
Küster coordinates the development of the database ProteomicsDB as well as the DKTK's Cancer Proteome Analysis Platform, which gives the researchers access to the substantial inhibitor data sets. The new data has already generated excitement in the clinical community: "This information is particularly important for patients with unusual genetic profiles," says Florian Bassermann, a senior physician at Klinikum Rechts der Isar, the university hospital of TU Munich. "Molecular tumor boards now have entirely new options for recommending the most suitable therapy for each individual patient."