Piper and Vismia species from Colombian Amazonia differentially affect cell proliferation of hepatocarcinoma cells

• Published in: Nutrients Vol. 7; no. 1; pp. 179 - 195
• Main Authors: Lizcano, Leandro J, Siles, Maite, Trepiana, Jenifer, Hernández, M Luisa, Navarro, Rosaura, Ruiz-Larrea, M Begoña, Ruiz-Sanz, José Ignacio
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 30.12.2014; MDPI
• Subjects: Animals; Antineoplastic Agents, Phytogenic - pharmacology; antioxidant activity; Antioxidants; Antioxidants - pharmacology; Carcinoma, Hepatocellular - pathology; catalase; Cell cycle; cell cycle arrest; Cell Cycle Checkpoints; Cell growth; Cell Line, Tumor; Cell Proliferation - drug effects; Clusiaceae - chemistry; Cytotoxicity; Enzymes; Flavonoids; flow cytometry; Folk medicine; free radical; Free radicals; Hep G2 Cells; Hepatocytes - drug effects; hepatoma cell line; Humans; Liver cancer; Male; Medicine; Natural products; Phenols; Physiology; Piper - chemistry; Plant Extracts - pharmacology; polyphenol; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species - metabolism; superoxide dismutase; Toxicity; Colombia; United States > US; Germany; Spain
• ISSN: 2072-6643; 2072-6643
• DOI: 10.3390/nu7010179

There is an increasing interest to identify plant-derived natural products with antitumor activities. In this work, we have studied the effects of aqueous leaf extracts from Amazonian Vismia and Piper species on human hepatocarcinoma cell toxicity. Results showed that, depending on the cell type, the plants displayed differential effects; thus, Vismia baccifera induced the selective killing of HepG2, while increasing cell growth of PLC-PRF and SK-HEP-1. In contrast, these two last cell lines were sensitive to the toxicity by Piper krukoffii and Piper putumayoense, while the Piperaceae did not affect HepG2 growth. All the extracts induced cytotoxicity to rat hepatoma McA-RH7777, but were innocuous (V. baccifera at concentrations < 75 µg/mL) or even protected cells from basal death (P. putumayoense) in primary cultures of rat hepatocytes. In every case, cytotoxicity was accompanied by an intracellular accumulation of reactive oxygen species (ROS). These results provide evidence for the anticancer activities of the studied plants on specific cell lines and suggest that cell killing could be mediated by ROS, thus involving mechanisms independent of the plants free radical scavenging activities. Results also support the use of these extracts of the Vismia and Piper genera with opposite effects as a model system to study the mechanisms of the antitumoral activity against different types of hepatocarcinoma.