| Literature DB >> 28408224 |
Lorenzo Botta1, Giorgio Maccari2, Pierpaolo Calandro2, Marika Tiberi2, Annalaura Brai2, Claudio Zamperini2, Filippo Canducci3, Mario Chiariello4, Rosa Martí-Centelles5, Eva Falomir5, Miguel Carda5.
Abstract
AIDS-related cancer diseases are malignancies with low incidence on healthy people that affect mostly subjects already immunocompromised. The connection between HIV/AIDS and these cancers has not been established yet, but a weakened immune system is certainly the main cause. We envisaged the possibility to screen a small library of compounds synthesized in our laboratory against opportunistic tumors mainly due to HIV infection like Burkitt's Lymphoma. From cellular assays and gene expression analysis we identified two promising compounds. These derivatives have the dual action required inhibiting HIV replication in human TZM-bl cells infected with HIV-1 NL4.3 and showing cytotoxic activity on human colon HT-29 and breast adenocarcinoma MCF-7 cells. In addition, preclinical in vitro adsorption, distribution, metabolism, and excretion studies highlighted a satisfactory pharmacokinetic profile.Entities:
Keywords: Burkitt’s Lymphoma; Cancer; HIV; c-Myc; hTERT
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Year: 2017 PMID: 28408224 DOI: 10.1016/j.bmcl.2017.03.097
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823