TACIMA-218: A Novel Pro-Oxidant Agent Exhibiting Selective Antitumoral Activity.
Jamilah AbusarahYun CuiNehme El-HachemAbed El-Hakim El-KadiryIan Hammond-MartelHugo WurteleAnnie BeaudryNoël J M RaynalFrancis RobertJerry PelletierMaja JankovicFrancois MercierSamaneh KamyabiazarBorhane AnnabiMoutih RafeiPublished in: Molecular cancer therapeutics (2020)
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.
Keyphrases
- cell death
- oxidative stress
- cell cycle arrest
- induced apoptosis
- nuclear factor
- anti inflammatory
- toll like receptor
- signaling pathway
- endoplasmic reticulum stress
- endothelial cells
- dna damage
- diabetic rats
- ischemia reperfusion injury
- papillary thyroid
- single cell
- small molecule
- diffuse large b cell lymphoma
- cell therapy
- squamous cell
- robot assisted
- pi k akt
- open label
- cell proliferation
- induced pluripotent stem cells
- diffusion weighted imaging
- cancer therapy
- magnetic resonance
- computed tomography
- high throughput
- magnetic resonance imaging
- stem cells
- mesenchymal stem cells
- squamous cell carcinoma
- randomized controlled trial
- young adults
- bone marrow
- skin cancer
- oxide nanoparticles