The Department of Microbiology and Immunology, McGill University, Montréal, Québec, Canada.
The Department of Pharmacology and Physiology, Université de Montréal, Montréal, Québec, Canada.
Mol Cancer Ther. 2021 Jan;20(1):37-49. doi: 10.1158/1535-7163.MCT-20-0333. Epub 2020 Oct 21.
We report the discovery, via a unique high-throughput screening strategy, of a novel bioactive anticancer compound: hiol lkylating ompound nducing assive poptosis (TACIMA)-218. We demonstrate that this molecule engenders apoptotic cell death in genetically diverse murine and human cancer cell lines, irrespective of their p53 status, while sparing normal cells. TACIMA-218 causes oxidative stress in the absence of protective antioxidants normally induced by Nuclear factor erythroid 2-related factor 2 activation. As such, TACIMA-218 represses RNA translation and triggers cell signaling cascade alterations in AKT, p38, and JNK pathways. In addition, TACIMA-218 manifests thiol-alkylating properties resulting in the disruption of redox homeostasis along with key metabolic pathways. When administered to immunocompetent animals as a monotherapy, TACIMA-218 has no apparent toxicity and induces complete regression of pre-established lymphoma and melanoma tumors. In sum, TACIMA-218 is a potent oxidative stress inducer capable of selective cancer cell targeting.
硫烷基化诱导大量细胞凋亡(TACIMA)-218。我们证明,这种分子在遗传上不同的鼠类和人类癌细胞系中引发凋亡细胞死亡,而不影响其 p53 状态,同时对正常细胞没有影响。TACIMA-218 在没有核因子红细胞 2 相关因子 2 激活通常诱导的保护性抗氧化剂的情况下引起氧化应激。因此,TACIMA-218 抑制 RNA 翻译,并触发 AKT、p38 和 JNK 途径中的细胞信号级联改变。此外,TACIMA-218 表现出硫烷基化特性,导致氧化还原稳态以及关键代谢途径的破坏。当作为单一疗法在免疫功能正常的动物中给药时,TACIMA-218 没有明显的毒性,并诱导已建立的淋巴瘤和黑色素瘤肿瘤的完全消退。总之,TACIMA-218 是一种有效的氧化应激诱导剂,能够选择性地靶向癌细胞。