Giarrizzo Michael, LaComb Joseph F, Patel Hetvi R, Reddy Rohan G, Haley John D, Graves Lee M, Iwanowicz Edwin J, Bialkowska Agnieszka B
Department of Medicine, Renaissance School of Medicine at Stony Brook University, Stony Brook, New York.
Department of Pathology, Stony Brook University, Stony Brook, New York.
Mol Cancer Ther. 2024 Dec 3;23(12):1761-1778. doi: 10.1158/1535-7163.MCT-24-0170.
Oxidative phosphorylation is an essential metabolic process for cancer proliferation and therapy resistance. The ClpXP complex maintains mitochondrial proteostasis by degrading misfolded proteins. Madera Therapeutics has developed a class of highly potent and selective small-molecule activators (TR compounds) of the ClpXP component caseinolytic peptidase proteolytic subunit (ClpP). This approach to cancer therapy eliminates substrate recognition and activates nonspecific protease function within mitochondria, which has shown encouraging preclinical efficacy in multiple malignancies. The class-leading compound TR-107 has demonstrated significantly improved potency in ClpP affinity and activation and enhanced pharmacokinetic properties over the multitargeting clinical agent ONC201. In this study, we investigate the in vitro efficacy of TR-107 against human colorectal cancer cells. TR-107 inhibited colorectal cancer cell proliferation in a dose- and time-dependent manner and induced cell cycle arrest at low nanomolar concentrations. Mechanistically, TR-107 downregulated the expression of proteins involved in the mitochondrial unfolded protein response and mitochondrial DNA transcription and translation. TR-107 attenuated oxygen consumption rate and glycolytic compensation, confirming inactivation of oxidative phosphorylation and a reduction in total cellular respiration. Multiomics analysis of treated cells indicated a downregulation of respiratory chain complex subunits and an upregulation of mitophagy and ferroptosis pathways. Further evaluation of ferroptosis revealed a depletion of antioxidant and iron toxicity defenses that could potentiate sensitivity to combinatory chemotherapeutics. Together, this study provides evidence and insight into the subcellular mechanisms employed by colorectal cancer cells in response to potent ClpP agonism. Our findings demonstrate a productive approach to disrupting mitochondrial metabolism, supporting the translational potential of TR-107.
氧化磷酸化是癌症增殖和治疗耐药性的重要代谢过程。ClpXP复合物通过降解错误折叠的蛋白质来维持线粒体蛋白质稳态。马德拉治疗公司开发了一类高效且选择性的小分子激活剂(TR化合物),可激活ClpXP组分酪蛋白水解肽酶蛋白水解亚基(ClpP)。这种癌症治疗方法消除了底物识别并激活线粒体内的非特异性蛋白酶功能,在多种恶性肿瘤中显示出令人鼓舞的临床前疗效。领先的化合物TR-107在ClpP亲和力和激活方面表现出显著提高的效力,并且与多靶点临床药物ONC201相比,其药代动力学特性得到了增强。在本研究中,我们研究了TR-107对人结肠癌细胞的体外疗效。TR-107以剂量和时间依赖性方式抑制结肠癌细胞增殖,并在低纳摩尔浓度下诱导细胞周期停滞。从机制上讲,TR-107下调了参与线粒体未折叠蛋白反应以及线粒体DNA转录和翻译的蛋白质表达。TR-107降低了氧消耗率和糖酵解补偿,证实了氧化磷酸化的失活以及总细胞呼吸的减少。对处理过的细胞进行的多组学分析表明,呼吸链复合物亚基下调,线粒体自噬和铁死亡途径上调。对铁死亡的进一步评估显示抗氧化剂和铁毒性防御的耗竭,这可能增强对联合化疗的敏感性。总之,本研究为结肠癌细胞对强效ClpP激动剂反应所采用的亚细胞机制提供了证据和见解。我们的研究结果证明了一种破坏线粒体代谢的有效方法,支持了TR-107的转化潜力。