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Cytotoxic constituents from Celastrus paniculatus induce apoptosis and autophagy in breast cancer cells
Institution:1. Laboratorio de Biología del Cáncer, Instituto de Investigaciones Bioquímicas Bahía Blanca, Centro Científico Tecnológico (INIBIBB-CCT-CONICET), Camino La Carrindanga Km. 7, 8000 Bahía Blanca, Argentina;2. Departamento de Química, Instituto de Química del Sur (INQUISUR-CONICET), Universidad Nacional del Sur, Av. Alem 1253, 8000 Bahía Blanca, Argentina;3. Servicio de Patología del Hospital Interzonal General de Agudos Dr. José Penna, Av. Lainez 2401, 8000 Bahía Blanca, Argentina;4. Departamento de Hematología, IACA, San Martín 68, 8000 Bahía Blanca, Argentina;5. Cátedra de Matemática, Departamento de Físico-Matemática, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Viamonte 444, C1053ABJ Ciudad autónoma de Buenos Aires, Argentina;6. Institute of Pharmaceutical Sciences, Albert-Ludwigs University Freiburg, Albertstrasse 25, 79104 Freiburg, Germany
Abstract:Celastrus paniculatus is a traditional medicinal plant with diverse pharmacological activities. To identify its bioactive constituents, three new β-dihydroagarofuranoid sesquiterpenes were isolated from the whole plant, of which the major constituent is (1α,2α,8β,9β)-1,8-bis(acetyloxy)-2,9-bis(benzoyloxy)-14-hydroxy-β-dihydroagarofuran. It was assessed for its antiproliferative activity, and it suppressed the viability of MCF-7 breast cancer cells with an IC50 of 17 ± 1 μM. This growth inhibition was, in part, attributable to apoptosis. Moreover, this drug treatment led to LC3B-II accumulation, indicative of autophagy. Western blot analysis established its ability to target a broad range of signaling effectors related to survival and cell cycle progression, including Akt, NF-κB, p53, and MAP kinases. In addition, flow cytometry analysis indicates increased reactive oxygen species production in response to this compound. Taken together, these findings suggest a pleiotropic mode of mechanism that underlies the antiproliferative activity of this compound in MCF-7 breast cancer cells.
Keywords:Celastraceae  Sesquiterpenes  Autophagy  Apoptosis
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