The new complex was identified as a controller of DNA repair processes using a precise measurement method (affinity purification mass spectrometry). "This also showed that the inhibition of these enzymes can prevent the repair of genetic material and cause the death of cells," says first author Terezia Vcelkova from MedUni Vienna's Center for Anatomy and Cell Biology describing a highly desirable effect in tumour cells. The genetic material, the DNA, is exposed to various harmful influences such as UV light or environmental pollutants on a daily basis. These influences can lead to changes in the DNA sequence, so-called mutations. To repair this damage to genetic material, various highly efficient biochemical repair mechanisms are normally activated. If these processes do not succeed in repairing the damage, programmed cell death (apoptosis) is ultimately initiated to protect against malignant cells. To ensure their survival, cells react to DNA damage by activating and integrating signalling pathways or signalling cascades.

 

This is achieved in particular through the activation of signalling pathways known as DNA damage response (or DDR). These signalling cascades are responsible for bringing repair factors to the right place in the genome at the right time in order to repair the mutated DNA efficiently and promptly. The control instances and regulators in this interaction are better defined thanks to the current research work. "The effectiveness of the novel cancer therapeutics based on this, which are intended to improve the response of tumour cells to cancer therapies, is now being tested in preclinical studies," says Christian Seiser about the next steps.