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Piper nigrum ethanolic extract rich in piperamides causes ROS overproduction, oxidative damage in DNA leading to cell cycle arrest and apoptosis in cancer cells
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 i...
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Published in: | Journal of ethnopharmacology 2016-08, Vol.189, p.139-147 |
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creator | de Souza Grinevicius, Valdelúcia Maria Alves Kviecinski, Maicon Roberto Santos Mota, Nádia Sandrini Ramos Ourique, Fabiana Porfirio Will Castro, Luiza Sheyla Evenni Andreguetti, Rafaela Rafognato Gomes Correia, João Francisco Filho, Danilo Wilhem Pich, Claus Tröger Pedrosa, Rozangela Curi |
description | 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.
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.
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.
Extraction yielded 64mg/g (36% piperine and 4.2% piperyline). Treatments caused DNA damage and reduced cell viability (EC50=27.1±2.0 and 80.5±6.6µg/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-xL 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.
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 G1/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.
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doi_str_mv | 10.1016/j.jep.2016.05.020 |
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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.
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.
Extraction yielded 64mg/g (36% piperine and 4.2% piperyline). Treatments caused DNA damage and reduced cell viability (EC50=27.1±2.0 and 80.5±6.6µg/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-xL 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.
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 G1/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.
[Display omitted]</description><identifier>ISSN: 0378-8741</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2016.05.020</identifier><identifier>PMID: 27178634</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animals ; Antineoplastic Agents, Phytogenic - isolation & purification ; Antineoplastic Agents, Phytogenic - pharmacology ; Antitumor activity ; Apoptosis ; Apoptosis - drug effects ; Apoptosis Regulatory Proteins - metabolism ; Biomarkers, Tumor - metabolism ; Breast Neoplasms - drug therapy ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Carcinoma, Ehrlich Tumor - drug therapy ; Carcinoma, Ehrlich Tumor - genetics ; Carcinoma, Ehrlich Tumor - metabolism ; Carcinoma, Ehrlich Tumor - pathology ; Cell cycle arrest ; Cell Cycle Checkpoints - drug effects ; Cell Cycle Proteins - metabolism ; DNA Damage ; Dose-Response Relationship, Drug ; Ethanol - chemistry ; Female ; HT29 Cells ; Humans ; Lipid Peroxidation - drug effects ; Male ; MCF-7 Cells ; Mice, Inbred BALB C ; Oxidants - isolation & purification ; Oxidants - pharmacology ; Oxidative Stress - drug effects ; Phytotherapy ; Piper nigrum ; Piper nigrum - chemistry ; Piperidines - isolation & purification ; Piperidines - pharmacology ; Plant Extracts - isolation & purification ; Plant Extracts - pharmacology ; Plants, Medicinal ; Protein Carbonylation - drug effects ; Reactive Oxygen Species - metabolism ; ROS overproduction ; Solvents - chemistry ; Time Factors ; Tumor Burden - drug effects ; Up-Regulation</subject><ispartof>Journal of ethnopharmacology, 2016-08, Vol.189, p.139-147</ispartof><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-31dda9a4175d23f4579c7a09039de5b71c9744e643158f18efbaa7af4271e8af3</citedby><cites>FETCH-LOGICAL-c462t-31dda9a4175d23f4579c7a09039de5b71c9744e643158f18efbaa7af4271e8af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27178634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Souza Grinevicius, Valdelúcia Maria Alves</creatorcontrib><creatorcontrib>Kviecinski, Maicon Roberto</creatorcontrib><creatorcontrib>Santos Mota, Nádia Sandrini Ramos</creatorcontrib><creatorcontrib>Ourique, Fabiana</creatorcontrib><creatorcontrib>Porfirio Will Castro, Luiza Sheyla Evenni</creatorcontrib><creatorcontrib>Andreguetti, Rafaela Rafognato</creatorcontrib><creatorcontrib>Gomes Correia, João Francisco</creatorcontrib><creatorcontrib>Filho, Danilo Wilhem</creatorcontrib><creatorcontrib>Pich, Claus Tröger</creatorcontrib><creatorcontrib>Pedrosa, Rozangela Curi</creatorcontrib><title>Piper nigrum ethanolic extract rich in piperamides causes ROS overproduction, oxidative damage in DNA leading to cell cycle arrest and apoptosis in cancer cells</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>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.
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.
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.
Extraction yielded 64mg/g (36% piperine and 4.2% piperyline). Treatments caused DNA damage and reduced cell viability (EC50=27.1±2.0 and 80.5±6.6µg/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-xL 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.
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 G1/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.
[Display omitted]</description><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - isolation & purification</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Antitumor activity</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis Regulatory Proteins - metabolism</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Carcinoma, Ehrlich Tumor - drug therapy</subject><subject>Carcinoma, Ehrlich Tumor - genetics</subject><subject>Carcinoma, Ehrlich Tumor - metabolism</subject><subject>Carcinoma, Ehrlich Tumor - pathology</subject><subject>Cell cycle arrest</subject><subject>Cell Cycle Checkpoints - drug effects</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>DNA Damage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Ethanol - chemistry</subject><subject>Female</subject><subject>HT29 Cells</subject><subject>Humans</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Male</subject><subject>MCF-7 Cells</subject><subject>Mice, Inbred BALB C</subject><subject>Oxidants - isolation & purification</subject><subject>Oxidants - pharmacology</subject><subject>Oxidative Stress - drug effects</subject><subject>Phytotherapy</subject><subject>Piper nigrum</subject><subject>Piper nigrum - chemistry</subject><subject>Piperidines - isolation & purification</subject><subject>Piperidines - pharmacology</subject><subject>Plant Extracts - isolation & purification</subject><subject>Plant Extracts - pharmacology</subject><subject>Plants, Medicinal</subject><subject>Protein Carbonylation - drug effects</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>ROS overproduction</subject><subject>Solvents - chemistry</subject><subject>Time Factors</subject><subject>Tumor Burden - drug effects</subject><subject>Up-Regulation</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhS0EokPhAdggL1mQYMfO2BGrquVPqijiZ23dsW-mHiVxsJ1R-zY8Ko6msGR17-I7R-feQ8hLzmrO-PbtoT7gXDdlrVlbs4Y9IhuuVVOpVonHZMOE0pVWkp-RZykdGGOKS_aUnDWKK70VckN-f_UzRjr5fVxGivkWpjB4S_EuR7CZRm9vqZ_ovGIweoeJWlhSGd9uvtNwxDjH4BabfZje0HDnHWR_ROpghD2u0qsvF3RAcH7a0xyoxWGg9t4OSCFGTJnC5CjMYc4h-bQqLEy2hFrJ9Jw86WFI-OJhnpOfH97_uPxUXd98_Hx5cV1ZuW1yJbhz0IHkqnWN6GWrOquAdUx0Dtud4rZTUuJWCt7qnmvsdwAKellegRp6cU5en3zLOb-WEsuMPq0JYMKwJMM151o2TOiC8hNqY0gpYm_m6EeI94YzsxZjDqYUY9ZiDGtNKaZoXj3YL7sR3T_F3yYK8O4EYDny6DGaZD2WPzgf0Wbjgv-P_R8oEKDf</recordid><startdate>20160802</startdate><enddate>20160802</enddate><creator>de Souza Grinevicius, Valdelúcia Maria Alves</creator><creator>Kviecinski, Maicon Roberto</creator><creator>Santos Mota, Nádia Sandrini Ramos</creator><creator>Ourique, Fabiana</creator><creator>Porfirio Will Castro, Luiza Sheyla Evenni</creator><creator>Andreguetti, Rafaela Rafognato</creator><creator>Gomes Correia, João Francisco</creator><creator>Filho, Danilo Wilhem</creator><creator>Pich, Claus Tröger</creator><creator>Pedrosa, Rozangela Curi</creator><general>Elsevier Ireland Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160802</creationdate><title>Piper nigrum ethanolic extract rich in piperamides causes ROS overproduction, oxidative damage in DNA leading to cell cycle arrest and apoptosis in cancer cells</title><author>de Souza Grinevicius, Valdelúcia Maria Alves ; Kviecinski, Maicon Roberto ; Santos Mota, Nádia Sandrini Ramos ; Ourique, Fabiana ; Porfirio Will Castro, Luiza Sheyla Evenni ; Andreguetti, Rafaela Rafognato ; Gomes Correia, João Francisco ; Filho, Danilo Wilhem ; Pich, Claus Tröger ; Pedrosa, Rozangela Curi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-31dda9a4175d23f4579c7a09039de5b71c9744e643158f18efbaa7af4271e8af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - isolation & purification</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Antitumor activity</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis Regulatory Proteins - metabolism</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Carcinoma, Ehrlich Tumor - drug therapy</topic><topic>Carcinoma, Ehrlich Tumor - genetics</topic><topic>Carcinoma, Ehrlich Tumor - metabolism</topic><topic>Carcinoma, Ehrlich Tumor - pathology</topic><topic>Cell cycle arrest</topic><topic>Cell Cycle Checkpoints - drug effects</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>DNA Damage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Ethanol - chemistry</topic><topic>Female</topic><topic>HT29 Cells</topic><topic>Humans</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Male</topic><topic>MCF-7 Cells</topic><topic>Mice, Inbred BALB C</topic><topic>Oxidants - isolation & purification</topic><topic>Oxidants - pharmacology</topic><topic>Oxidative Stress - drug effects</topic><topic>Phytotherapy</topic><topic>Piper nigrum</topic><topic>Piper nigrum - chemistry</topic><topic>Piperidines - isolation & purification</topic><topic>Piperidines - pharmacology</topic><topic>Plant Extracts - isolation & purification</topic><topic>Plant Extracts - pharmacology</topic><topic>Plants, Medicinal</topic><topic>Protein Carbonylation - drug effects</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>ROS overproduction</topic><topic>Solvents - chemistry</topic><topic>Time Factors</topic><topic>Tumor Burden - drug effects</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Souza Grinevicius, Valdelúcia Maria Alves</creatorcontrib><creatorcontrib>Kviecinski, Maicon Roberto</creatorcontrib><creatorcontrib>Santos Mota, Nádia Sandrini Ramos</creatorcontrib><creatorcontrib>Ourique, Fabiana</creatorcontrib><creatorcontrib>Porfirio Will Castro, Luiza Sheyla Evenni</creatorcontrib><creatorcontrib>Andreguetti, Rafaela Rafognato</creatorcontrib><creatorcontrib>Gomes Correia, João Francisco</creatorcontrib><creatorcontrib>Filho, Danilo Wilhem</creatorcontrib><creatorcontrib>Pich, Claus Tröger</creatorcontrib><creatorcontrib>Pedrosa, Rozangela Curi</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of ethnopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Souza Grinevicius, Valdelúcia Maria Alves</au><au>Kviecinski, Maicon Roberto</au><au>Santos Mota, Nádia Sandrini Ramos</au><au>Ourique, Fabiana</au><au>Porfirio Will Castro, Luiza Sheyla Evenni</au><au>Andreguetti, Rafaela Rafognato</au><au>Gomes Correia, João Francisco</au><au>Filho, Danilo Wilhem</au><au>Pich, Claus Tröger</au><au>Pedrosa, Rozangela Curi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Piper nigrum ethanolic extract rich in piperamides causes ROS overproduction, oxidative damage in DNA leading to cell cycle arrest and apoptosis in cancer cells</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2016-08-02</date><risdate>2016</risdate><volume>189</volume><spage>139</spage><epage>147</epage><pages>139-147</pages><issn>0378-8741</issn><eissn>1872-7573</eissn><abstract>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.
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.
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.
Extraction yielded 64mg/g (36% piperine and 4.2% piperyline). Treatments caused DNA damage and reduced cell viability (EC50=27.1±2.0 and 80.5±6.6µg/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-xL 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.
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 G1/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.
[Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>27178634</pmid><doi>10.1016/j.jep.2016.05.020</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list) |
subjects | Animals Antineoplastic Agents, Phytogenic - isolation & purification Antineoplastic Agents, Phytogenic - pharmacology Antitumor activity Apoptosis Apoptosis - drug effects Apoptosis Regulatory Proteins - metabolism Biomarkers, Tumor - metabolism Breast Neoplasms - drug therapy Breast Neoplasms - genetics Breast Neoplasms - metabolism Breast Neoplasms - pathology Carcinoma, Ehrlich Tumor - drug therapy Carcinoma, Ehrlich Tumor - genetics Carcinoma, Ehrlich Tumor - metabolism Carcinoma, Ehrlich Tumor - pathology Cell cycle arrest Cell Cycle Checkpoints - drug effects Cell Cycle Proteins - metabolism DNA Damage Dose-Response Relationship, Drug Ethanol - chemistry Female HT29 Cells Humans Lipid Peroxidation - drug effects Male MCF-7 Cells Mice, Inbred BALB C Oxidants - isolation & purification Oxidants - pharmacology Oxidative Stress - drug effects Phytotherapy Piper nigrum Piper nigrum - chemistry Piperidines - isolation & purification Piperidines - pharmacology Plant Extracts - isolation & purification Plant Extracts - pharmacology Plants, Medicinal Protein Carbonylation - drug effects Reactive Oxygen Species - metabolism ROS overproduction Solvents - chemistry Time Factors Tumor Burden - drug effects Up-Regulation |
title | Piper nigrum ethanolic extract rich in piperamides causes ROS overproduction, oxidative damage in DNA leading to cell cycle arrest and apoptosis in cancer cells |
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