Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario L5L 1C6, Canada.
Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York 14853, United States.
J Med Chem. 2022 Jul 14;65(13):8855-8868. doi: 10.1021/acs.jmedchem.1c01965. Epub 2022 Jun 14.
Human carboxylesterase 2 (hCES2) converts anticancer prodrugs, such as irinotecan, into their active metabolites phase I drug metabolism. Owing to interindividual variability, hCES2 serves as a predictive marker of patient response to hCES2-activated prodrug-based therapy, whereby a low intratumoral hCES2 activity leads to therapeutic resistance. Despite the ability to identify nonresponders, effective treatments for resistant patients are needed. Clinically approved photodynamic therapy is an attractive alternative for irinotecan-resistant patients. Here, we describe the application of our hCES2-selective small-molecule ratiometric fluorescent chemosensor, , as a single theranostic agent given its discovered functionality as a photosensitizer. produces singlet oxygen and induces photocytotoxicity in cancer cells in a strong negative correlation with hCES2 activity. Two-photon excitation of produces fluorescence, singlet oxygen, and photocytotoxicity in tumor spheroids. Overall, serves as a novel theranostic agent with selective photocytotoxicity in hCES2-prodrug resistant cancer cells, making a promising agent for applications.
人羧酸酯酶 2(hCES2)将抗癌前药(如伊立替康)转化为其活性代谢物,即 I 相药物代谢。由于个体间的差异,hCES2 是预测患者对 hCES2 激活前药治疗反应的标志物,低肿瘤内 hCES2 活性导致治疗抵抗。尽管能够识别无反应者,但需要针对耐药患者的有效治疗方法。临床批准的光动力疗法是伊立替康耐药患者的一种有吸引力的替代方法。在这里,我们描述了我们的 hCES2 选择性小分子比率荧光化学传感器的应用, ,因为它具有作为光增敏剂的发现功能,所以被用作单一的治疗诊断试剂。 在强负相关于 hCES2 活性的情况下产生单线态氧并诱导癌细胞光细胞毒性。 的双光子激发在肿瘤球体中产生荧光、单线态氧和光细胞毒性。总体而言, 作为一种新型的治疗诊断试剂,对 hCES2 前药耐药的癌细胞具有选择性光细胞毒性,使 成为一种有前途的应用试剂。