Many tumour cells mist themselves with a protective perfume that disables the immune system.
But a drug already approved for other purposes can apparently render this weapon harmless.
This is shown in a study by the University of Bonn and the University Medical Center Hamburg-Eppendorf, which has now appeared in the Journal for ImmunoTherapy of Cancer.
The researchers now want to further optimise the compound.
In the medium term, this could pave the way for new anti-cancer drugs.
Many cancer cells surround themselves with a dense cloud of adenosine.
On the one hand, the molecule suppresses the immune system.
At the same time, it stimulates the formation of new blood vessels that supply the tumour with oxygen and nutrients.
It also ensures that the malignant cells migrate to other organs and form metastases there.
Adenosine is produced from adenosine triphosphate, or ATP for short.
Tumour cells secrete large amounts of it.
They carry various enzymes on their surface that then convert the ATP to adenosine in several steps.
One of these is known as CD39. "It catalyses the first of the conversion steps," explains Prof Dr Christa Müller from the Institute of Pharmacy at the University of Bonn. "If CD39 is inhibited, hardly any adenosine is produced."
Around the globe, pharmaceutical researchers are therefore searching for an active ingredient that slows down CD39.
Because without adenosine, tumours would no longer be protected from the immune system.
"Instead, ATP would accumulate around the cancer cells, which would actually stimulate the immune response," says Müller. "So the body's own defenses would not be suppressed; on the contrary, they would be turned on extra sharp."
So far, the search has been largely unsuccessful.
The Bonn research group therefore pursued a new search strategy in the study: "There are other enzymes in the body than CD39 that also process ATP," explains Laura Schäkel. The collaborator of Prof Müller carried out many of the central experiments in the study. "These include, for example, the so-called protein kinases. The nice thing is that there are already approved drugs that inhibit protein kinases. We now looked at whether they also work against CD39."
At the start of the study, there were a total of 50 different agents approved for certain diseases that inhibit protein kinases.
The research group examined all of them.
With success: "One of the substances, ceritinib, also blocks the conversion of ATP by CD39," Schäkel is pleased to report. "We were able to show this not only in the test tube, but also in cultures with so-called triple-negative breast cancer cells. These are extremely difficult to treat - they usually hardly respond to therapies."
Nevertheless, Christa Müller does not think it makes sense to simply administer ceritinib as a CD39 inhibitor in certain cancers. "After all, the active ingredient is primarily directed against a different group of enzymes; it would therefore have undesirable side effects," she says. "We now want to modify it so that it hardly inhibits protein kinases at all and instead slows down CD39 even more."
Such an optimised active ingredient could also be combined with other therapeutic agents. "Classic cytostatics usually massively weaken the immune system; CD39 blockers, on the other hand, would activate it," says Prof. Müller, who is also a member of the Transdisciplinary Research Areas (TRA) "Building Blocks of Matter" and "Life and Health." "In combination, therefore, the drugs could possibly have a significantly greater effect."
Before use, moreover, it would first be possible to measure whether the cancer cells of affected patients actually carry a lot of CD39 on their surface. "Because only then would treatment with CD39 inhibitors make sense," says Müller. "So you would tailor the administration to the individual patient. This personalisation of therapies for the purpose of enhancing efficiency is becoming increasingly important in medicine."
Article: Protein kinase inhibitor ceritinib blocks ectonucleotidase CD39 – a promising target for cancer immunotherapy
Source: University of Bonn
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