Dilly Sébastien, Romero Miguel, Solier Stéphanie, Feron Olivier, Dessy Chantal, Slama Schwok Anny
Gustave Roussy Cancer Center, CNRS UMR 8200, F-94805 Villejuif, France.
Pole of Pharmacology and Therapeutics (FATH), Institute of Experimental and Clinical Research (IREC), Université Catholique de Louvain, B-1200 Brussels, Belgium.
Antioxidants (Basel). 2023 Feb 10;12(2):440. doi: 10.3390/antiox12020440.
ROS in cancer cells play a key role in pathways regulating cell death, stemness maintenance, and metabolic reprogramming, all of which have been implicated in resistance to chemo/ immunotherapy. Adjusting ROS levels to reverse the resistance of cancer cells without impairing normal cell functions is a new therapeutic avenue. In this paper, we describe new inhibitors of NADPH oxidase (NOX), a key enzyme in many cells of the tumor microenvironment. The first inhibitor, called Nanoshutter-1, NS1, decreased the level of tumor-promoting "M2" macrophages differentiated from human blood monocytes. NS1 disrupted the active NADPH oxidase-2 (NOX2) complex at the membrane and in the mitochondria of the macrophages, as shown by confocal microscopy. As one of the characteristics of tumor invasion is hypoxia, we tested whether NS1 would affect vascular reactivity by reducing ROS or NO levels in wire and pressure myograph experiments on isolated blood vessels. The results show that NS1 vasodilated blood vessels and would likely reduce hypoxia. Finally, as both NOX2 and NOX4 are key proteins in tumors and their microenvironment, we investigated whether NS1 would probe these proteins differently. Models of NOX2 and NOX4 were generated by homology modeling, showing structural differences at their C-terminal NADPH site, in particular in their last Phe. Thus, the NADPH site presents an unexploited chemical space for addressing ligand specificity, which we exploited to design a novel NOX2-specific inhibitor targeting variable NOX2 residues. With the proper smart vehicle to target specific cells of the microenvironment as TAMs, NOX2-specific inhibitors could open the way to new precision therapies.
活性氧(ROS)在癌细胞中对调节细胞死亡、干性维持和代谢重编程的信号通路起着关键作用,而所有这些都与化疗/免疫治疗耐药性有关。在不损害正常细胞功能的情况下调节ROS水平以逆转癌细胞的耐药性是一条新的治疗途径。在本文中,我们描述了一种新型烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶(NOX)抑制剂,该酶是肿瘤微环境中许多细胞的关键酶。第一种抑制剂名为Nanoshutter-1(NS1),它降低了从人血单核细胞分化而来的促肿瘤“M2”巨噬细胞的水平。共聚焦显微镜显示,NS1破坏了巨噬细胞膜和线粒体中活性NADPH氧化酶-2(NOX2)复合物。由于肿瘤侵袭的特征之一是缺氧,我们在离体血管的线式和压力肌动描记实验中测试了NS1是否会通过降低ROS或一氧化氮(NO)水平来影响血管反应性。结果表明,NS1使血管舒张,可能会减轻缺氧。最后,由于NOX2和NOX4都是肿瘤及其微环境中的关键蛋白,我们研究了NS1是否会以不同方式作用于这些蛋白。通过同源建模生成了NOX2和NOX4模型,结果显示它们在C端NADPH位点存在结构差异,特别是在其最后一个苯丙氨酸(Phe)处。因此,NADPH位点提供了一个尚未开发的化学空间来解决配体特异性问题,我们利用这一空间设计了一种针对可变NOX2残基的新型NOX2特异性抑制剂。借助合适的智能载体靶向微环境中的特定细胞,如肿瘤相关巨噬细胞(TAM),NOX2特异性抑制剂可能为新的精准治疗开辟道路。