Designing PARP-specific inhibitors would enhance their effectiveness against cancer

IMIM researchers show that PARP-1 or PARP-2 specific deficiency in T lymphocytes results in better antitumor response than depleting both forms.

PARP inhibitors are considered a potential treatment for cancer. | Picture by National Cancer Institute from Unsplash.

PARP inhibitors are considered a potential treatment for cancer. | Picture by National Cancer Institute from Unsplash.

In order to make our cells work properly, we need many enzymes. Poly (ADP-ribose) polymerase (PARP) is a family of enzymes involved in some cellular processes such as DNA repair. Since this family has key functions in cell division, scientists have designed PARP inhibitors, which are considered a potential treatment for cancer.

Recently, researchers at the Hospital del Mar Medical Research Institute (IMIM) have proved that specific PARP-1 or PARP-2 deficiency — PARP family members — in T lymphocytes results in better antitumor response. On the other hand, they found a worse antitumour response when there was a double deficiency of PARP-1 and PARP-2 in T lymphocytes.

“All current PARP inhibitor drugs act in the same way against both proteins, PARP-1 and PARP-2. However, our results show that it would be very important to develop more selective drugs in order to specifically inhibit PARP-1 or PARP-2, thus achieving a better response against the tumor”, concludes José Yelamos, research group coordinator at IMIM and leader of the study.

 

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