| Literature DB >> 33087510 |
Jamilah Abusarah1, Yun Cui2, Nehme El-Hachem3,4, Abed El-Hakim El-Kadiry2, Ian Hammond-Martel5,6, Hugo Wurtele5,7, Annie Beaudry2, Noël J-M Raynal2, Francis Robert8, Jerry Pelletier8, Maja Jankovic9,10, Francois Mercier9,10, Samaneh Kamyabiazar11, Borhane Annabi11, Moutih Rafei12,2,6,13.
Abstract
We report the discovery, via a unique high-throughput screening strategy, of a novel bioactive anticancer compound: Thiol Alkylating Compound Inducing Massive Apoptosis (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. ©2020 American Association for Cancer Research.Entities:
Year: 2020 PMID: 33087510 DOI: 10.1158/1535-7163.MCT-20-0333
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261