The SYNTRAIN network officially started September 1st, 2016. 15 fellows have worked in beneficiary laboratories in order to carry out the individual projects. The kickoff meeting was held in April 2017 in Copenhagen, which marked the joint initiation of research projects, and the project came to an end in November 2020. During the execution of these projects, we identified new molecular cancer targets, obtained understanding of their mechanism and function, and, importantly, also developed compounds to achieve the aim. The research has been carried out by the highly selected group of 15 talented young researchers. 3 Summer schools have been held for advanced training, and fellows have participated in major international conference with several already presenting their exciting work. During the period, the consortium has contributed to the international scientific community environment by organizing a symposium on “DNA repair and synthetic lethality in cancer” and latest, an international online conference on “Genomic Instability in Cancer: from tumour evolution to novel cures”.
Our network progressed very well in the first period scientifically, and has now advanced further through the final period with excellent outcomes and results. The following section describes the three research work packages and their outcomes. The first focused on identification of novel synthetic lethal interactions with DNA replication stress to identify proteins with potential to be relevant targets for cancer therapy. 8 tasks were outlined in this work package, all tasks are well completed. The second research work package aimed to obtain mechanistic insights regarding the biological roles of genes involved in synthetic lethal interactions with homologous recombination repair deficiencies and/or DNA replication stress. This work package entailed 13 tasks, all have seen remarkable progress. Finally, the last research work package aimed at identifying and testing chemical compounds with activity against biological targets involved in synthetic lethal interactions with homologous recombination repair deficiencies and/or DNA replication stress. There were 8 tasks, and compound screens were carried out with promising leads being established, also for tasks connected with projects advancing from the second work package. At this stage 17 publications have been accepted and published on fellow projects, and additional manuscripts are in revision and expected to be published in 2021 and 2022. Furthermore the consortium members have so far submitted two patent applications, of which one has been granted.