Piper nigrum ethanolic extract rich in piperamides causes ROS overproduction, oxidative damage in DNA leading to cell cycle arrest and apoptosis in cancer cells

被引:65
作者
Alves de Souza Grinevicius, Valdelucia Maria [1 ]
Kviecinski, Maicon Roberto [2 ]
Ramos Santos Mota, Nadia Sandrini [1 ]
Ourique, Fabiana [1 ]
Porfirio Will Castro, Luiza Sheyla Evenni [1 ]
Andreguetti, Rafaela Rafognato [1 ]
Gomes Correia, Joao Francisco [1 ]
Wilhem Filho, Danilo [3 ]
Pich, Claus Troger [4 ]
Pedrosa, Rozangela Curi [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Bioquim, Lab Bioquim Expt, Florianopolis, SC, Brazil
[2] Univ Sul Santa Catarina UNISUL, Programa Posgrad Ciencias Saude, Florianopolis, SC, Brazil
[3] Univ Fed Santa Catarina, Dept Ecol & Zool, Florianopolis, SC, Brazil
[4] Univ Fed Santa Catarina, NITBIO, Ararangua, SC, Brazil
关键词
Piper nigrum; ROS overproduction; DNA damage; Cell cycle arrest; Apoptosis; Antitumor activity; TANDEM MASS-SPECTROMETRY; MEDICINAL-PLANTS; COMMUNITY; PROTEINS; STRESS; FAMILY; ASSAY;
D O I
10.1016/j.jep.2016.05.020
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: Ayurvedic and Chinese traditional medicine and tribal people use herbal preparations containing Piper nigrum fruits for the treatment of many health disorders like inflammation, fever, asthma and cancer. In Brazil, traditional maroon culture associates the spice Piper nigrum to health recovery and inflammation attenuation. Aims of the study: The aim of the current work was to evaluate the relationship between reactive oxygen species (ROS) overproduction, DNA fragmentation, cell cycle arrest and apoptosis induced by Piper nigrum ethanolic extract and its antitumor activity. Methods: The plant was macerated in ethanol. Extract constitution was assessed by TLC, UV-vis and ESI-IT-MS/MS spectrometry. The cytotoxicity, proliferation and intracellular ROS generation was evaluated in MCF-7 cells. DNA damage effects were evaluated through intercalation into CT-DNA, plasmid DNA cleavage and oxidative damage in CT-DNA. Tumor growth inhibition, survival time increase, apoptosis, cell cycle arrest and oxidative stress were assessed in Ehrlich ascites carcinoma-bearing mice. Results: Extraction yielded 64 mg/g (36% piperine and 4.2% piperyline). Treatments caused DNA damage and reduced cell viability (EC50=27.1 +/- 2.0 and 80.5 +/- 6.6 mu g/ml in MCF-7 and HT-29 cells, respectively), inhibiting cell proliferation by 57% and increased ROS generation in MCF-7 cells (65%). Ehrlich carcinoma was inhibited by the extract, which caused reduction of tumor growth (60%), elevated survival time (76%), cell cycle arrest and induced apoptosis. The treatment with extract increased Bax and p53 and inhibited Bcl-x(L), and cyclin A expression. It also induced an oxidative stress in vivo verified as enhanced lipid peroxidation and carbonyl proteins content and increased activities of glutathione reductase, superoxide dismutase and catalase. GSH concentration was decreased in tumor tissue from mice. Conclusion: The ethanolic extract has cytotoxic and antiproliferative effect on MCF-7 cells and antitumor effect in vivo probably due to ROS overproduction that induced oxidative stress affecting key proteins involved in cell cycle arrest at Gl/S and triggering apoptosis. Finally, the overall data from this study are well in line with the traditional claims for the antitumor effect of Piper nigrum fruits. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:139 / 147
页数:9
相关论文
共 50 条
[1]
[Anonymous], METHODS ENZYMOL
[2]
Da Silva NCB, 2012, B LATINOAM CARIBE PL, V11, P435
[3]
Bertini I., 2012, PLOS ONE, V6
[4]
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[5]
Bird R P., 1984, Method Enzymol, V90, P105, DOI [10.1016/S0076-6879(84)05038-2, DOI 10.1016/S0076-6879(84)05038-2]
[6]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]
Brown R, 1997, BRIT MED BULL, V53, P466
[8]
CARLBERG I, 1985, METHOD ENZYMOL, V113, P484
[9]
Metabolic profiling of Piper species by direct analysis using real time mass spectrometry combined with principal component analysis [J].
Chandra, Preeti ;
Bajpai, Vikas ;
Srivastva, Mukesh ;
Kumar, K. B. Ramesh ;
Kumar, Brijesh .
ANALYTICAL METHODS, 2014, 6 (12) :4234-4239
[10]
Chaveerach A., 2006, Ethnobotany Research and Applications, V4, P223