Antitumoral Potential of Artepillin C, a Compound Derived from Brazilian Propolis, against Breast Cancer Cell Lines

Author:

de Freitas Meirelles Lyvia Eloiza1,de Assis Carvalho Analine Rosa Barquez1,Ferreira Damke Gabrielle Marconi Zago1,Souza Raquel Pantarotto1,Damke Edilson1,de Souza Bonfim-Mendonça Patrícia1,de Oliveira Dembogurski Djaceli Sampaio2,da Silva Denise Brentan2,Consolaro Marcia Edilaine Lopes1,da Silva Vania Ramos Sela1

Affiliation:

1. Department of Clinical Analysis and Biomedicine, Universidade Estadual de Maringá (UEM), Maringá, Paraná, Brazil

2. Laboratory of Natural Products and Mass Spectrometry (LAPNEM), Universidade Federal do Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil

Abstract

Background:: Breast cancer is the most commonly diagnosed cancer among women worldwide with limited treatment options. Artepillin C (3,5-diprenyl-4-hydroxycinnamic acid) is one of the main constituents of Brazilian propolis presenting different activities, including antitumoral effects against various types of cancer. Objective:: We evaluated the antitumoral potential and mechanisms of action of artepillin C against two distinct human breast cancer cell lines, MCF-7 and MDA-MB-231, to explore a new therapeutic candidate. Methods:: Cell viability was assessed by MTT assay and the long-term cytotoxicity was performed by clonogenic assay. The morphological changes were observed by light microscopy, analysis of cell death pathway by Annexin V FITC/propidium iodide (PI), lactate dehydrogenase (LDH) by colorimetry, DNA fragmentation by agarose gel and senescence by β-galactosidase. Detection of total reactive oxygen species (ROS) by fluorescence microscopy and determination of mitochondrial transmembrane potential by flow cytometry were also performed. Results:: Artepillin C presented a strong and dose-time-dependent cytotoxic effect on MCF-7 and MDA-MB-231 cell lines, with cytotoxicity more evident in MCF-7. In both cancer cell lines, the clonogenic potential was significantly reduced and the morphology of the cells was changed. The treatment also induced death by necrosis and late apoptosis in MCF-7 and MDA-MB-231 and induced cell senescence in MCF-7. Also, artepillin C increased total ROS in both cancer cells and decreased mitochondrial membrane potential in MDA-MB-231 cells. Conclusion:: Artepillin C presented antitumoral potential in two human breast cancer cell lines, MCF-7, and MDA-MB-231, suggesting a new promising option for the treatment and/or chemopreventive strategy for breast cancer.

Publisher

Bentham Science Publishers Ltd.

Subject

Cancer Research,Pharmacology,Molecular Medicine

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