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Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29)
The dibenzylbutyrolactone lignan (-)-cubebin, which is extracted from the seeds of the pepper Piper cubeba, has shown promise as an anti-inflammatory, analgesic, leishmanicidal, antiproliferative, and trypanocidal compound. Given the therapeutic potential of (-)-cubebin, this study aimed to investig...
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Published in: | Journal of Toxicology and Environmental Health, Part A Part A, 2016, Vol.79 (2), p.92-100 |
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container_title | Journal of Toxicology and Environmental Health, Part A |
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creator | Niwa, Andressa Megumi de Paula, Natalia Aparecida Vesenick, Diogo Campos Sartori, Daniele Maistro, Edson Luis Ribeiro, Lúcia Regina Mantovani, Mário Sérgio |
description | The dibenzylbutyrolactone lignan (-)-cubebin, which is extracted from the seeds of the pepper Piper cubeba, has shown promise as an anti-inflammatory, analgesic, leishmanicidal, antiproliferative, and trypanocidal compound. Given the therapeutic potential of (-)-cubebin, this study aimed to investigate its safety profile by analyzing cytotoxicity, mutagenicity, cell proliferation kinetics, induction of apoptosis, and expression of pro-apoptotic genes in human colon adenocarcinoma cells (HT29) exposed to (-)-cubebin. MTT cytotoxicity assays demonstrated that (-)-cubebin was cytotoxic only at 280 µM, whereas it was not cytotoxic at 2.8, 14, or 28 µM. Data demonstrated that (-)-cubebin was not mutagenic as evidenced by a micronucleus (MN) assay, did not alter cell-growth kinetics over 4 d, and showed absence of induced apoptosis after 24 h. Further, CASP8 and CASP9 gene expression was not markedly changed in HT29 cells exposed to 28 µM or 70 µM (-)-cubebin for 12 h. Based on our observations, (-)-cubebin was cytotoxic at a concentration of 280 µM, suggesting that the use of this concentration should be avoided. However, lower concentrations exerted no apparent damaging effects, indicating that this lignan is safe to use for pharmacological purposes at certain concentrations. |
doi_str_mv | 10.1080/15287394.2015.1110067 |
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However, lower concentrations exerted no apparent damaging effects, indicating that this lignan is safe to use for pharmacological purposes at certain concentrations.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Assaying</subject><subject>Caspase 8 - biosynthesis</subject><subject>Caspase 9 - biosynthesis</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Colon</subject><subject>Colonic Neoplasms - drug therapy</subject><subject>DNA - drug effects</subject><subject>Exposure</subject><subject>Gene expression</subject><subject>Genes</subject><subject>HT29 Cells</subject><subject>Human</subject><subject>Humans</subject><subject>Lignans</subject><subject>Lignans - pharmacology</subject><subject>Micronucleus Tests</subject><subject>Piper - chemistry</subject><subject>Piper cubeba</subject><issn>1528-7394</issn><issn>1087-2620</issn><issn>2381-3504</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkT1vFDEQhi0EIiHwE0CWaC7FHuOPtb0dKAoEKRIUobZsrx0c7dqHvQvk3-PjLhQUiMojzfOOZ_Qg9JLAloCCN6SnSrKBbymQfksIARDyETptTdlRQeFxqxvT7aET9KzWOwAgfBBP0QkVikip1Cm6vfxuptUsMSecA57ibTIJb7rzzq3W25iw_7kU4xY_4lDyjD_HnS_4d9PgFvq6zi3g8tRqM_qUnSkupjwb7Pw0Vby5uqHD-XP0JJip-hfH9wx9eX95c3HVXX_68PHi3XXnuIClGxTlTjIOzAk-cNYOkT21TBDBLR_BEWKsgZ4oAX1g3gfpLLVWAQtCKM_O0OYwd1fyt9XXRc-x7hcxyee1aiIHRiVVQP8DlUxRwWjf0Nd_oXd5Lakd0ijRC0KoGBrVHyhXcq3FB70rcTblXhPQe2n6QZreS9NHaS336jh9tbMf_6QeLDXg7QGIKeQymx-5TKNezP2USygmuVg1-_cfvwByRKJ_</recordid><startdate>2016</startdate><enddate>2016</enddate><creator>Niwa, Andressa Megumi</creator><creator>de Paula, Natalia Aparecida</creator><creator>Vesenick, Diogo Campos</creator><creator>Sartori, Daniele</creator><creator>Maistro, Edson Luis</creator><creator>Ribeiro, Lúcia Regina</creator><creator>Mantovani, Mário Sérgio</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><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>7QF</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7ST</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TV</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>SOI</scope><scope>7T2</scope><scope>7U2</scope></search><sort><creationdate>2016</creationdate><title>Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29)</title><author>Niwa, Andressa Megumi ; 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Given the therapeutic potential of (-)-cubebin, this study aimed to investigate its safety profile by analyzing cytotoxicity, mutagenicity, cell proliferation kinetics, induction of apoptosis, and expression of pro-apoptotic genes in human colon adenocarcinoma cells (HT29) exposed to (-)-cubebin. MTT cytotoxicity assays demonstrated that (-)-cubebin was cytotoxic only at 280 µM, whereas it was not cytotoxic at 2.8, 14, or 28 µM. Data demonstrated that (-)-cubebin was not mutagenic as evidenced by a micronucleus (MN) assay, did not alter cell-growth kinetics over 4 d, and showed absence of induced apoptosis after 24 h. Further, CASP8 and CASP9 gene expression was not markedly changed in HT29 cells exposed to 28 µM or 70 µM (-)-cubebin for 12 h. Based on our observations, (-)-cubebin was cytotoxic at a concentration of 280 µM, suggesting that the use of this concentration should be avoided. However, lower concentrations exerted no apparent damaging effects, indicating that this lignan is safe to use for pharmacological purposes at certain concentrations.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>26817788</pmid><doi>10.1080/15287394.2015.1110067</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - drug therapy Antineoplastic Agents, Phytogenic - pharmacology Apoptosis Apoptosis - drug effects Assaying Caspase 8 - biosynthesis Caspase 9 - biosynthesis Cell Proliferation - drug effects Cell Survival - drug effects Colon Colonic Neoplasms - drug therapy DNA - drug effects Exposure Gene expression Genes HT29 Cells Human Humans Lignans Lignans - pharmacology Micronucleus Tests Piper - chemistry Piper cubeba |
title | Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
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