Achilles heel of anaplastic large-cell lymphoma (ALCL) cells identified

Anaplastic large-cell lymphomas (ALCL) are rare cancers of the white blood cells. New research from the international ERIA consortium, led by scientists in Vienna, has now shown that the same signaling pathway is essential to the growth of cancer cells in various forms of ALCL: TYK2 (tyrosine kinase 2, an important component of the immune system) prevents apoptotic cell death by increasing the production of Mcl1, a special type of protein belonging to the BCL2 family. Due to its unique enzymatic composition, TYK2 is therefore an interesting therapeutic target, making TYK2-specific inhibitors highly promising as new therapeutic agents in ALCL.

A particularly fruitful area of personalised medicine is cancer treatment, where improved diagnostic methods are able to break cancers down into increasingly smaller subcategories, thereby making it possible to apply individual treatment strategies. The molecular analysis of human tumour samples has therefore become a focus of cancer research, to identify new therapeutic targets and validate them in tumour models, in order to improve the clinical management of cancer patients. However, this faces clinicians with several challenges, including increasingly comprehensive diagnostics as well as the problem of adequately validating this data for smaller patient groups. This is all the more urgent in the case of rare cancers such as ALCL, where the number of patients is so small.

Nicole Prutsch and Olaf Merkel from the Medical University of Vienna and their international colleagues have now reported in the journal Leukemia that, rather than finding yet another subdivision of the ALCL subgroups, they have managed to identify a common actor in ALCL patients. TYK2 is not only expressed in all patients but produces the same anti-apoptotic reaction, which keeps the lymphoma cells alive and so helps the tumour to grow.

“We were therefore able to regard the TYK2 signals as the Achilles heel of ALCL, since both types of ALCL that we investigated relied on its activity to maintain the essential signal to protect against cell death,” explains Olaf Merkel, who is co-last author of this publication together with Lukas Kenner. Attenuating the TYK2 signal in the cell culture resulted in rapid cell death and, in ALCL model mice, in which TYK2 was genetically switched off, the researchers observed that the laboratory animals survived for longer.

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