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TACIMA-218:一种新型促氧化剂,具有选择性抗肿瘤活性。

TACIMA-218: A Novel Pro-Oxidant Agent Exhibiting Selective Antitumoral Activity.

机构信息

The Department of Microbiology and Immunology, McGill University, Montréal, Québec, Canada.

The Department of Pharmacology and Physiology, Université de Montréal, Montréal, Québec, Canada.

出版信息

Mol Cancer Ther. 2021 Jan;20(1):37-49. doi: 10.1158/1535-7163.MCT-20-0333. Epub 2020 Oct 21.

DOI:10.1158/1535-7163.MCT-20-0333
PMID:33087510
Abstract

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.

摘要

我们通过一种独特的高通量筛选策略发现了一种新型的生物活性抗癌化合物

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。

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