PT - JOURNAL ARTICLE AU - Narjis Fatima AU - Yandong Shen AU - Kyle Crassini AU - Edwin J. Iwanowicz AU - Henk Lang AU - Donald S. Karanewsky AU - Richard I Christopherson AU - Stephen P Mulligan AU - O. Giles Best TI - The CIpP activator, TR-57, is highly effective as a single agent and in combination with venetoclax against CLL cells <em>in vitro</em> AID - 10.1101/2022.03.07.483345 DP - 2022 Jan 01 TA - bioRxiv PG - 2022.03.07.483345 4099 - http://biorxiv.org/content/early/2022/03/07/2022.03.07.483345.short 4100 - http://biorxiv.org/content/early/2022/03/07/2022.03.07.483345.full AB - Despite advances in treatment, a significant proportion of patients with chronic lymphocytic leukaemia (CLL) will relapse with drug-resistant disease.Recent studies demonstrate that the imipridones ONC-201 and ONC-212 and the more potent TR-compounds are effective against a range of different cancers, including acute myeloid leukaemia and tumours of the brain, breast, and prostate. These drugs induce cell death through inhibition of mitochondrial function and activation of the mitochondrial protease, caseinolytic protease (CIpP), and the unfolded protein response (UPR).Here we demonstrate that a drug in this class, TR-57, has efficacy as a single agent and is synergistic with venetoclax against CLL cells cultured under in vitro conditions that mimic the tumour microenvironment. The inhibitory effects of TR-57 on cell survival, proliferation and migration were irrespective of poor-risk features, including aberrations of TP53. Changes in protein expression suggest the mechanisms of action of TR-57 and its synergy with venetoclax involve activation of the UPR, inhibition of the AKT and ERK1/2 pathways and a pro-apoptotic shift in expression of proteins of the BCL-2 family.The study suggests TR-57, as a single agent and in combination with venetoclax, may represent an effective treatment option for CLL, including for patients with poor-risk disease.Competing Interest StatementThe authors have declared no competing interest.