A Novel Sulfonyl-Based Small Molecule Exhibiting Anti-cancer Properties
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Frontiers Media S.A.
Abstract
Phenotypic screening is an ideal strategy for the discovery of novel bioactive molecules. Using a customized high-throughput screening (HTS) assay employing primary T lymphocytes, we screened a small library of 4,398 compounds with unknown biological function/target to identify compounds eliciting immunomodulatory properties and discovered a sulfonyl-containing hit, we named InhiTinib. This compound inhibited interferon (IFN)-gamma production and proliferation of primary CD3+ T cells without inducing cell death. In contrast, InhiTinib triggered apoptosis in several murine and human cancer cell lines. Besides, the compound was well tolerated by immunocompetent mice, triggered tumor regression in animals with pre-established EL4 T-cell lymphomas, and prolonged the overall survival of mice harboring advanced tumors. Altogether, our data demonstrate the anti-cancer properties of InhiTinib, which can henceforth bridge to wider-scale biochemical and clinical tests following further in-depth pharmacodynamic studies. © Copyright © 2020 El-Kadiry, Abusarah, Cui, El-Hachem, Hammond-Martel, Wurtele, Thomas, Ahmadi, Balood, Talbot and Rafei.
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Apoptosis, Cancer, Hts, Small molecule, Sulfonyl compound, T cells, Antineoplastic agent, Gamma interferon, Inhitinib, Unclassified drug, Animal cell, Animal experiment, Animal model, Animal tissue, Antineoplastic activity, Article, Bone marrow, Cd3+ t lymphocyte, Cell proliferation assay, Cytokine production, Drug dose comparison, Drug efficacy, Drug mechanism, Drug megadose, Drug tolerability, Female, Fluorescence, High throughput screening, Human, Human cell, Immunomodulation, In vitro study, In vivo study, Low drug dose, Lymphocyte proliferation, Mouse, Nerve cell culture, Nonhuman, Overall survival, Oxidative stress, Pharmacodynamics, Spinal ganglion, Spleen, T cell lymphoma, Thymus, Tumor regression, Western blotting