Tumour cells have several genetic mutations, one of the effects of which is unbridled cell growth. One of the tumour cell’s “weak spots” is that large amounts of defective proteins are produced. These proteins are broken down by proteasomes, the cell’s “waste disposal units” for proteins. The researchers have identified a molecule called b-AP15 which inhibits the cell’s ability to feed the protein waste into the proteasomes. The waste then accumulates, which leads to the death of the tumour cells via apoptosis. More precisely, b-AP15 inhibits the deubiquitinating enzymes USP14 and UCHL5 of the proteasomes. The study demonstrates that b-AP15-inhibited tumour growth in four separate animal models, which suggests that the substance could be used for treating cancer.
The substance was also shown able to kill off tumour cells that are resistant to a currently used cancer drug that inhibits the proteasome by another mechanism.

“This newly discovered mechanism of action is very promising,” says Stig Linder, professor of experimental oncology at the Department of Oncology and Pathology at Karolinska Institutet. “However, I should like to stress that we’re unable to treat patients with our substances at present. But we hope that our continuing work will eventually lead to the development of new drugs.”

The study has been conducted as a collaboration between researchers at Karolinska Institutet, Uppsala University and the Istituto Nazionale per Studio e Cura dei Tumori in Milan.

For further information, contact:
Professor Stig Linder
Department of Oncology and Pathology
Karolinska Institutet
Tel: +46 (0)8 517 724 52, +46 (0)70 4841275

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Karolinska Institutet is one of the world’s leading medical universities. It accounts for over 40 per cent of the medical academic research conducted in Sweden and offers the country’s broadest range of education in medicine and health sciences. Since 1901 the Nobel Assembly at Karolinska Institutet has selected the Nobel laureates in Physiology or Medicine.