Novel Lignan and Stilbenoid Mixture Shows Anticarcinogenic Efficacy in Preclinical PC-3M-luc2 Prostate Cancer Model: e93764

Prostate cancer is the most common cancer of men in the Western world, and novel approaches for prostate cancer risk reduction are needed. Plant-derived phenolic compounds attenuate prostate cancer growth in preclinical models by several mechanisms, which is in line with epidemiological findings sug...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2014-04, Vol.9 (4)
Hauptverfasser: Yatkin, Emrah, Polari, Lauri, Laajala, Teemu D, Smeds, Annika, Eckerman, Christer, Holmbom, Bjarne, Saarinen, Niina M, Aittokallio, Tero, Maekelae, Sari I
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 4
container_start_page
container_title PloS one
container_volume 9
creator Yatkin, Emrah
Polari, Lauri
Laajala, Teemu D
Smeds, Annika
Eckerman, Christer
Holmbom, Bjarne
Saarinen, Niina M
Aittokallio, Tero
Maekelae, Sari I
description Prostate cancer is the most common cancer of men in the Western world, and novel approaches for prostate cancer risk reduction are needed. Plant-derived phenolic compounds attenuate prostate cancer growth in preclinical models by several mechanisms, which is in line with epidemiological findings suggesting that consumption of plant-based diets is associated with low risk of prostate cancer. The objective of this study was to assess the effects of a novel lignan-stilbenoid mixture in PC-3M-luc2 human prostate cancer cells in vitro and in orthotopic xenografts. Lignan and stilbenoid -rich extract was obtained from Scots pine (Pinus sylvestris) knots. Pine knot extract as well as stilbenoids (methyl pinosylvin and pinosylvin), and lignans (matairesinol and nortrachelogenin) present in pine knot extract showed antiproliferative and proapoptotic efficacy at greater than or equal to 40 mu M concentration in vitro. Furthermore, pine knot extract derived stilbenoids enhanced tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induced apoptosis already at greater than or equal to 10 mu M concentrations. In orthotopic PC-3M-luc2 xenograft bearing immunocompromized mice, three-week peroral exposure to pine knot extract (52 mg of lignans and stilbenoids per kg of body weight) was well tolerated and showed anti-tumorigenic efficacy, demonstrated by multivariate analysis combining essential markers of tumor growth (i.e. tumor volume, vascularization, and cell proliferation). Methyl pinosylvin, pinosylvin, matairesinol, nortrachelogenin, as well as resveratrol, a metabolite of pinosylvin, were detected in serum at total concentration of 7-73 mu M, confirming the bioavailability of pine knot extract derived lignans and stilbenoids. In summary, our data indicates that pine knot extract is a novel and cost-effective source of resveratrol, methyl pinosylvin and other bioactive lignans and stilbenoids. Pine knot extract shows anticarcinogenic efficacy in preclinical prostate cancer model, and our in vitro data suggests that compounds derived from the extract may have potential as novel chemosensitizers to TRAIL. These findings promote further research on health-related applications of wood biochemicals.
doi_str_mv 10.1371/journal.pone.0093764
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1544014911</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1544014911</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_15440149113</originalsourceid><addsrcrecordid>eNqVzstKw0AUxvFBEKyXN3Bxlm4SZzJpatxJqLhopFD3ZZyc1CnjOXUuXvDlDeILuPrgx7f4C3GpZKn0Ql3vOQcyvjwwYSllqxdNfSRmqtVV0VRSn4jTGPdSzvVN08zE9yO_o4eV25EhMDTAJjn_jMRugN59phwQNi_8EeGOkrMmWEe8Q3IWluM4gf0CR7AOaL2b1HhYd4XuC59tNTHHZBJCZ8higJ4H9LeAv1nn4ng0PuLF356Jq_vlU_dQHAK_ZYxp--qiRe8NIee4VfO6lqpuldL_uP4AlApYHw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1544014911</pqid></control><display><type>article</type><title>Novel Lignan and Stilbenoid Mixture Shows Anticarcinogenic Efficacy in Preclinical PC-3M-luc2 Prostate Cancer Model: e93764</title><source>DOAJ Directory of Open Access Journals</source><source>Public Library of Science (PLoS)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Yatkin, Emrah ; Polari, Lauri ; Laajala, Teemu D ; Smeds, Annika ; Eckerman, Christer ; Holmbom, Bjarne ; Saarinen, Niina M ; Aittokallio, Tero ; Maekelae, Sari I</creator><creatorcontrib>Yatkin, Emrah ; Polari, Lauri ; Laajala, Teemu D ; Smeds, Annika ; Eckerman, Christer ; Holmbom, Bjarne ; Saarinen, Niina M ; Aittokallio, Tero ; Maekelae, Sari I</creatorcontrib><description>Prostate cancer is the most common cancer of men in the Western world, and novel approaches for prostate cancer risk reduction are needed. Plant-derived phenolic compounds attenuate prostate cancer growth in preclinical models by several mechanisms, which is in line with epidemiological findings suggesting that consumption of plant-based diets is associated with low risk of prostate cancer. The objective of this study was to assess the effects of a novel lignan-stilbenoid mixture in PC-3M-luc2 human prostate cancer cells in vitro and in orthotopic xenografts. Lignan and stilbenoid -rich extract was obtained from Scots pine (Pinus sylvestris) knots. Pine knot extract as well as stilbenoids (methyl pinosylvin and pinosylvin), and lignans (matairesinol and nortrachelogenin) present in pine knot extract showed antiproliferative and proapoptotic efficacy at greater than or equal to 40 mu M concentration in vitro. Furthermore, pine knot extract derived stilbenoids enhanced tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induced apoptosis already at greater than or equal to 10 mu M concentrations. In orthotopic PC-3M-luc2 xenograft bearing immunocompromized mice, three-week peroral exposure to pine knot extract (52 mg of lignans and stilbenoids per kg of body weight) was well tolerated and showed anti-tumorigenic efficacy, demonstrated by multivariate analysis combining essential markers of tumor growth (i.e. tumor volume, vascularization, and cell proliferation). Methyl pinosylvin, pinosylvin, matairesinol, nortrachelogenin, as well as resveratrol, a metabolite of pinosylvin, were detected in serum at total concentration of 7-73 mu M, confirming the bioavailability of pine knot extract derived lignans and stilbenoids. In summary, our data indicates that pine knot extract is a novel and cost-effective source of resveratrol, methyl pinosylvin and other bioactive lignans and stilbenoids. Pine knot extract shows anticarcinogenic efficacy in preclinical prostate cancer model, and our in vitro data suggests that compounds derived from the extract may have potential as novel chemosensitizers to TRAIL. These findings promote further research on health-related applications of wood biochemicals.</description><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0093764</identifier><language>eng</language><subject>Pinus sylvestris</subject><ispartof>PloS one, 2014-04, Vol.9 (4)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27922,27923</link.rule.ids></links><search><creatorcontrib>Yatkin, Emrah</creatorcontrib><creatorcontrib>Polari, Lauri</creatorcontrib><creatorcontrib>Laajala, Teemu D</creatorcontrib><creatorcontrib>Smeds, Annika</creatorcontrib><creatorcontrib>Eckerman, Christer</creatorcontrib><creatorcontrib>Holmbom, Bjarne</creatorcontrib><creatorcontrib>Saarinen, Niina M</creatorcontrib><creatorcontrib>Aittokallio, Tero</creatorcontrib><creatorcontrib>Maekelae, Sari I</creatorcontrib><title>Novel Lignan and Stilbenoid Mixture Shows Anticarcinogenic Efficacy in Preclinical PC-3M-luc2 Prostate Cancer Model: e93764</title><title>PloS one</title><description>Prostate cancer is the most common cancer of men in the Western world, and novel approaches for prostate cancer risk reduction are needed. Plant-derived phenolic compounds attenuate prostate cancer growth in preclinical models by several mechanisms, which is in line with epidemiological findings suggesting that consumption of plant-based diets is associated with low risk of prostate cancer. The objective of this study was to assess the effects of a novel lignan-stilbenoid mixture in PC-3M-luc2 human prostate cancer cells in vitro and in orthotopic xenografts. Lignan and stilbenoid -rich extract was obtained from Scots pine (Pinus sylvestris) knots. Pine knot extract as well as stilbenoids (methyl pinosylvin and pinosylvin), and lignans (matairesinol and nortrachelogenin) present in pine knot extract showed antiproliferative and proapoptotic efficacy at greater than or equal to 40 mu M concentration in vitro. Furthermore, pine knot extract derived stilbenoids enhanced tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induced apoptosis already at greater than or equal to 10 mu M concentrations. In orthotopic PC-3M-luc2 xenograft bearing immunocompromized mice, three-week peroral exposure to pine knot extract (52 mg of lignans and stilbenoids per kg of body weight) was well tolerated and showed anti-tumorigenic efficacy, demonstrated by multivariate analysis combining essential markers of tumor growth (i.e. tumor volume, vascularization, and cell proliferation). Methyl pinosylvin, pinosylvin, matairesinol, nortrachelogenin, as well as resveratrol, a metabolite of pinosylvin, were detected in serum at total concentration of 7-73 mu M, confirming the bioavailability of pine knot extract derived lignans and stilbenoids. In summary, our data indicates that pine knot extract is a novel and cost-effective source of resveratrol, methyl pinosylvin and other bioactive lignans and stilbenoids. Pine knot extract shows anticarcinogenic efficacy in preclinical prostate cancer model, and our in vitro data suggests that compounds derived from the extract may have potential as novel chemosensitizers to TRAIL. These findings promote further research on health-related applications of wood biochemicals.</description><subject>Pinus sylvestris</subject><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqVzstKw0AUxvFBEKyXN3Bxlm4SZzJpatxJqLhopFD3ZZyc1CnjOXUuXvDlDeILuPrgx7f4C3GpZKn0Ql3vOQcyvjwwYSllqxdNfSRmqtVV0VRSn4jTGPdSzvVN08zE9yO_o4eV25EhMDTAJjn_jMRugN59phwQNi_8EeGOkrMmWEe8Q3IWluM4gf0CR7AOaL2b1HhYd4XuC59tNTHHZBJCZ8higJ4H9LeAv1nn4ng0PuLF356Jq_vlU_dQHAK_ZYxp--qiRe8NIee4VfO6lqpuldL_uP4AlApYHw</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Yatkin, Emrah</creator><creator>Polari, Lauri</creator><creator>Laajala, Teemu D</creator><creator>Smeds, Annika</creator><creator>Eckerman, Christer</creator><creator>Holmbom, Bjarne</creator><creator>Saarinen, Niina M</creator><creator>Aittokallio, Tero</creator><creator>Maekelae, Sari I</creator><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20140401</creationdate><title>Novel Lignan and Stilbenoid Mixture Shows Anticarcinogenic Efficacy in Preclinical PC-3M-luc2 Prostate Cancer Model: e93764</title><author>Yatkin, Emrah ; Polari, Lauri ; Laajala, Teemu D ; Smeds, Annika ; Eckerman, Christer ; Holmbom, Bjarne ; Saarinen, Niina M ; Aittokallio, Tero ; Maekelae, Sari I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_15440149113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Pinus sylvestris</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yatkin, Emrah</creatorcontrib><creatorcontrib>Polari, Lauri</creatorcontrib><creatorcontrib>Laajala, Teemu D</creatorcontrib><creatorcontrib>Smeds, Annika</creatorcontrib><creatorcontrib>Eckerman, Christer</creatorcontrib><creatorcontrib>Holmbom, Bjarne</creatorcontrib><creatorcontrib>Saarinen, Niina M</creatorcontrib><creatorcontrib>Aittokallio, Tero</creatorcontrib><creatorcontrib>Maekelae, Sari I</creatorcontrib><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yatkin, Emrah</au><au>Polari, Lauri</au><au>Laajala, Teemu D</au><au>Smeds, Annika</au><au>Eckerman, Christer</au><au>Holmbom, Bjarne</au><au>Saarinen, Niina M</au><au>Aittokallio, Tero</au><au>Maekelae, Sari I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel Lignan and Stilbenoid Mixture Shows Anticarcinogenic Efficacy in Preclinical PC-3M-luc2 Prostate Cancer Model: e93764</atitle><jtitle>PloS one</jtitle><date>2014-04-01</date><risdate>2014</risdate><volume>9</volume><issue>4</issue><eissn>1932-6203</eissn><abstract>Prostate cancer is the most common cancer of men in the Western world, and novel approaches for prostate cancer risk reduction are needed. Plant-derived phenolic compounds attenuate prostate cancer growth in preclinical models by several mechanisms, which is in line with epidemiological findings suggesting that consumption of plant-based diets is associated with low risk of prostate cancer. The objective of this study was to assess the effects of a novel lignan-stilbenoid mixture in PC-3M-luc2 human prostate cancer cells in vitro and in orthotopic xenografts. Lignan and stilbenoid -rich extract was obtained from Scots pine (Pinus sylvestris) knots. Pine knot extract as well as stilbenoids (methyl pinosylvin and pinosylvin), and lignans (matairesinol and nortrachelogenin) present in pine knot extract showed antiproliferative and proapoptotic efficacy at greater than or equal to 40 mu M concentration in vitro. Furthermore, pine knot extract derived stilbenoids enhanced tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induced apoptosis already at greater than or equal to 10 mu M concentrations. In orthotopic PC-3M-luc2 xenograft bearing immunocompromized mice, three-week peroral exposure to pine knot extract (52 mg of lignans and stilbenoids per kg of body weight) was well tolerated and showed anti-tumorigenic efficacy, demonstrated by multivariate analysis combining essential markers of tumor growth (i.e. tumor volume, vascularization, and cell proliferation). Methyl pinosylvin, pinosylvin, matairesinol, nortrachelogenin, as well as resveratrol, a metabolite of pinosylvin, were detected in serum at total concentration of 7-73 mu M, confirming the bioavailability of pine knot extract derived lignans and stilbenoids. In summary, our data indicates that pine knot extract is a novel and cost-effective source of resveratrol, methyl pinosylvin and other bioactive lignans and stilbenoids. Pine knot extract shows anticarcinogenic efficacy in preclinical prostate cancer model, and our in vitro data suggests that compounds derived from the extract may have potential as novel chemosensitizers to TRAIL. These findings promote further research on health-related applications of wood biochemicals.</abstract><doi>10.1371/journal.pone.0093764</doi></addata></record>
fulltext fulltext
identifier EISSN: 1932-6203
ispartof PloS one, 2014-04, Vol.9 (4)
issn 1932-6203
language eng
recordid cdi_proquest_miscellaneous_1544014911
source DOAJ Directory of Open Access Journals; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects Pinus sylvestris
title Novel Lignan and Stilbenoid Mixture Shows Anticarcinogenic Efficacy in Preclinical PC-3M-luc2 Prostate Cancer Model: e93764
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T23%3A47%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20Lignan%20and%20Stilbenoid%20Mixture%20Shows%20Anticarcinogenic%20Efficacy%20in%20Preclinical%20PC-3M-luc2%20Prostate%20Cancer%20Model:%20e93764&rft.jtitle=PloS%20one&rft.au=Yatkin,%20Emrah&rft.date=2014-04-01&rft.volume=9&rft.issue=4&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0093764&rft_dat=%3Cproquest%3E1544014911%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1544014911&rft_id=info:pmid/&rfr_iscdi=true