OKN-007 is an Effective Anticancer Therapeutic Agent Targeting Inflammatory and Immune Metabolism Pathways in Endometrial Cancer.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacology and Experimental Therapeutics Pub Date : 2024-07-19 DOI:10.1124/jpet.124.002223
Sugantha Priya Elayapillai, Anjalika Gandhi, Samrita Dogra, Debra Saunders, Nataliya Smith, Cole Hladik, Rheal A Towner, Katherine M Moxley, Bethany N Hannafon
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Abstract

Advanced-stage endometrial cancer patients typically receive a combination of platinum and paclitaxel chemotherapy. However, limited treatment options are available for those with recurrent disease, and there is a need to identify alternative treatment options for the advanced setting. Our goal was to evaluate the pre-clinical efficacy and mechanism of action of Oklahoma Nitrone 007 (OKN-007) alone and in combination with carboplatin and paclitaxel in endometrial cancer. The effect of OKN-007 on the metabolic viability of endometrial cancer cells in both two- and three-dimensional (2D and 3D) cultures, as well as on clonogenic growth, in vitro was assessed. We also evaluated OKN-007 in vivo using an intraperitoneal xenograft model and targeted gene expression profiling to determine the molecular mechanism and gene expression programs altered by OKN-007. Our results showed that endometrial cancer cells were generally sensitive to OKN-007 in both 2D and 3D cultures. OKN-007 displayed a reduction in 3D spheroid and clonogenic growth. Subsequent targeted gene expression profiling revealed that OKN-007 significantly downregulated the immunosuppressive and immunometabolic enzyme indolamine 2,3-dioxygenase 1 (IDO1) (-11.27-fold change) and modulated upstream inflammatory pathways that regulate IDO1 expression (interferon- (IFN-), Jak-STAT, TGF-β, and NF-kB), downstream IDO1 effector pathways (mTOR and aryl hydrocarbon receptor (AhR)) and altered T-cell co-signaling pathways. OKN-007 treatment reduced IDO1, SULF2, and TGF-β protein expression in vivo, and inhibited TGF-β, NF-kB, and AhR- receptor-mediated nuclear signaling in vitro. These findings indicate that OKN-007 surmounts pro-inflammatory, immunosuppressive, and pro-tumorigenic pathways and is a promising approach for the effective treat endometrial cancer. Significance Statement Women with advanced and recurrent endometrial cancer have limited therapeutic options. OKN-007, which has minimal toxicity and is currently being evaluated in early-phase clinical trials for the treatment of cancer, is a potential new strategy for the treatment of endometrial cancer.

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OKN-007 是一种针对子宫内膜癌中炎症和免疫代谢途径的有效抗癌治疗剂。
晚期子宫内膜癌患者通常会接受铂和紫杉醇联合化疗。然而,复发性疾病患者的治疗方案有限,因此需要确定晚期的替代治疗方案。我们的目标是评估 Oklahoma Nitrone 007(OKN-007)单独或与卡铂和紫杉醇联合治疗子宫内膜癌的临床前疗效和作用机制。我们在体外评估了 OKN-007 对子宫内膜癌细胞在二维和三维(2D 和 3D )培养物中的代谢活力以及克隆性生长的影响。我们还利用腹腔异种移植模型和靶向基因表达谱分析对 OKN-007 进行了体内评估,以确定 OKN-007 改变的分子机制和基因表达程序。结果表明,在二维和三维培养中,子宫内膜癌细胞对 OKN-007 普遍敏感。OKN-007 可减少三维球形和克隆性生长。随后的靶向基因表达谱分析显示,OKN-007 能显著下调免疫抑制和免疫代谢酶吲哚胺 2,3- 二氧酶 1(IDO1)(-11.27倍的变化),并调节调控IDO1表达的上游炎症通路(干扰素(IFN-)、Jak-STAT、TGF-β和NF-kB)、IDO1下游效应通路(mTOR和芳基烃受体(AhR))以及改变的T细胞协同信号通路。OKN-007治疗可减少体内IDO1、SULF2和TGF-β蛋白的表达,并抑制体外TGF-β、NF-kB和AhR受体介导的核信号转导。这些研究结果表明,OKN-007 可克服促炎症、免疫抑制和促致癌通路,是有效治疗子宫内膜癌的一种很有前景的方法。意义声明 晚期和复发性子宫内膜癌妇女的治疗选择有限。OKN-007 毒性极低,目前正在早期癌症治疗临床试验中进行评估,是治疗子宫内膜癌的一种潜在新策略。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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