Antignani Antonella, Mathews Griner Lesley, Guha Rajarshi, Simon Nathan, Pasetto Matteo, Keller Jonathan, Huang Manjie, Angelus Evan, Pastan Ira, Ferrer Marc, FitzGerald David J, Thomas Craig J
Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4264, United States of America.
Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, 20850, United States of America.
PLoS One. 2016 Aug 24;11(8):e0161415. doi: 10.1371/journal.pone.0161415. eCollection 2016.
The intersection of small molecular weight drugs and antibody-based therapeutics is rarely studied in large scale. Both types of agents are currently part of the cancer armamentarium. However, very little is known about how to combine them in optimal ways. Immunotoxins are antibody-toxin gene fusion proteins engineered to target cancer cells via antibody binding to surface antigens. For fusion proteins derived from Pseudomonas exotoxin (PE), potency relies on the enzymatic domain of the toxin which catalyzes the ADP-ribosylation of EF2 causing inhibition of protein synthesis leading to cell death. Candidate immunotoxins have demonstrated clear value in clinical trials but generally have not been curative as single agents. Therefore we undertook three screens to discover effective combinations that could act synergistically. From the MIPE-3 library of compounds we identified various enhancers of immunotoxin action and at least one major class of inhibitor. Follow-up experiments confirmed the screening data and suggested that immunotoxins when administered with everolimus or nilotinib exhibit favorable combinatory activity and would be candidates for preclinical development. Mechanistic studies revealed that everolimus-immunotoxin combinations acted synergistically on elements of the protein synthetic machinery, including S61 kinase and 4E-BP1 of the mTORC1 pathway. Conversely, PARP inhibitors antagonized immunotoxins and also blocked the toxicity due to native ADP-ribosylating toxins. Thus, our goal of investigating a chemical library was justified based on the identification of several approved compounds that could be developed preclinically as 'enhancers' and at least one class of mitigator to be avoided.
小分子药物与基于抗体的治疗方法的交叉研究很少大规模进行。这两类药物目前都是癌症治疗手段的一部分。然而,对于如何以最佳方式将它们联合使用,人们知之甚少。免疫毒素是抗体 - 毒素基因融合蛋白,通过抗体与表面抗原结合来靶向癌细胞。对于源自铜绿假单胞菌外毒素(PE)的融合蛋白,其效力依赖于毒素的酶结构域,该结构域催化EF2的ADP核糖基化,导致蛋白质合成抑制,进而导致细胞死亡。候选免疫毒素在临床试验中已显示出明确的价值,但通常作为单一药物并不能治愈疾病。因此,我们进行了三项筛选,以发现可协同作用的有效组合。从MIPE - 3化合物库中,我们鉴定出了各种免疫毒素作用增强剂和至少一类抑制剂。后续实验证实了筛选数据,并表明免疫毒素与依维莫司或尼洛替尼联合使用时表现出良好的联合活性,有望成为临床前开发的候选药物。机制研究表明,依维莫司 - 免疫毒素组合对蛋白质合成机制的元件具有协同作用,包括mTORC1途径的S61激酶和4E - BP1。相反,PARP抑制剂拮抗免疫毒素,并也阻断了天然ADP核糖基化毒素的毒性。因此,基于鉴定出几种可在临床前开发为“增强剂”的已批准化合物以及至少一类应避免的减轻剂,我们对化学文库进行研究的目标是合理的。