A novel dopamine receptor D2 antagonist (ONC206) potentiates the effects of olaparib in endometrial cancer. Issue 1 (31st December 2023)

• Record Type: Journal Article
• Authors: Paraghamian, Sarah E.; Qiu, Jianqing; Hawkins, Gabrielle M.; Zhao, Ziyi; Sun, Wenchuan; Fan, Yali; Zhang, Xin; Suo, Hongyan; Hao, Tianran; Prabhu, Varun Vijay; Allen, Joshua E.; Zhou, Chunxiao; Bae-Jump, Victoria
• Is Part Of: Cancer biology & therapy. Volume 24:Issue 1(2023)
• Publication Date: 2023-12-31
• Subjects: ONC206 -- olaparib -- synergy -- apoptosis -- endometrial cancer; 616.99406
• DOI: 10.1080/15384047.2023.2202104
• Languages: English
• ISSNs: 1538-4047

Abstract

ABSTRACT: Poly ADP-ribose polymerase (PARP) inhibitors are effective therapies for cancer patients with homologous recombination (HR) deficient tumors. The imipridone ONC206 is an orally bioavailable dopamine receptor D2 antagonist and mitochondrial protease ClpP agonist that has anti-tumorigenic effects in endometrial cancer via induction of apoptosis, activation of the integrated stress response and modulation of PI3K/AKT signaling. Both PARP inhibitors and imipridones are being evaluated in endometrial cancer clinical trials but have yet to be explored in combination. In this manuscript, we evaluated the effects of the PARP inhibitor olaparib in combination with ONC206 in human endometrioid endometrial cancer cell lines and in a genetically engineered mouse model of endometrial cancer. Our results showed that simultaneous exposure of endometrial cancer cells to olaparib and ONC206 resulted in synergistic anti-proliferative effects and increased cellular stress and apoptosis in both cell lines, compared to either drug alone. The combination treatment also decreased expression of the anti-apoptotic protein Bcl-2 and reduced phosphorylation of AKT and S6, with greater effects compared to either drug alone. In the transgenic model of endometrial cancer, the combination of olaparib and ONC206 resulted in a more significant reduction in tumor weight in obese and lean mice compared to ONC206 alone or olaparib alone, together with a considerably decreased Ki-67 and enhanced H2AX expression in obese and lean mice. These results suggest that this novel dual therapy may be worthy of further exploration in clinical trials.