Back to Search
Start Over
TACIMA-218: A Novel Pro-Oxidant Agent Exhibiting Selective Antitumoral Activity
- Source :
- Molecular Cancer Therapeutics. 20:37-49
- Publication Year :
- 2021
- Publisher :
- American Association for Cancer Research (AACR), 2021.
-
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.
- Subjects :
- 0301 basic medicine
Cancer Research
Cell signaling
Alkylation
NF-E2-Related Factor 2
p38 mitogen-activated protein kinases
Antineoplastic Agents
medicine.disease_cause
Mice
03 medical and health sciences
0302 clinical medicine
Cell Line, Tumor
medicine
Animals
Humans
Cysteine
Sulfhydryl Compounds
Protein kinase B
Cell Death
Chemistry
Endoplasmic Reticulum Stress
Oxidants
Pro-oxidant
Chromatin
Mitochondria
Oxidative Stress
Phenotype
030104 developmental biology
Oncology
Apoptosis
Cell culture
030220 oncology & carcinogenesis
Cancer cell
Cancer research
Reactive Oxygen Species
Glycolysis
Protein Processing, Post-Translational
Heme Oxygenase-1
Oxidative stress
Subjects
Details
- ISSN :
- 15388514 and 15357163
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- Molecular Cancer Therapeutics
- Accession number :
- edsair.doi.dedup.....9dc7dc173dc3f4ae7aab289dc7c64329
- Full Text :
- https://doi.org/10.1158/1535-7163.mct-20-0333