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Chemistry and biology of ophiobolin A and its congeners
Authors:Marco Masi  Ramesh Dasari  Antonio Evidente  Veronique Mathieu  Alexander Kornienko
Affiliation:1. Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Universitario Monte Sant’Angelo, Via Cintia 4, 80126 Napoli, Italy;2. Department of Chemistry and Biochemistry, Texas State University, San Marcos, TX 78666, USA;3. Department of Pharmacotherapy and Pharmaceutics, Faculté de Pharmacie, Université Libre de Bruxelles (ULB), Brussels, Belgium;4. Department of Chemistry, North Caucasus Federal University, 1a Pushkin St, Stavropol 355009, Russian Federation;5. dULB Cancer Research Center, Université Libre de Bruxelles, Brussels, Belgium
Abstract:Ophiobolin A is a fungal secondary metabolite that was found to have significant activity against apoptosis-resistant glioblastoma cells through the induction of a non-apoptotic cell death, offering an innovative strategy to combat this aggressive cancer. The current article aims to make the bridge between the anti-cancer effects of ophiobolin A and its unique reaction with primary amines and suggests that pyrrolylation of lysine residues on its intracellular target protein(s) and/or phosphatidylethanolamine lipid is responsible for its biological effects. The article also discusses chemical derivatization of ophiobolin A to establish first synthetically generated structure-activity relationship. Finally, the reported total synthesis efforts toward the ophiobolin class of sesterterpenes are discussed and identified as a fertile area for improvement in pursuit of these molecules as anticancer agents.
Keywords:Anticancer activity  Apoptosis resistance  Glioblastoma  Ophiobolin A  Sesterterpenes
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