Grape Seed Proanthocyanidins Inhibit the Growth of Human Non-Small Cell Lung Cancer Xenografts by Targeting Insulin-Like Growth Factor Binding Protein-3, Tumor Cell Proliferation, and Angiogenic Factors

Purpose: Lung cancer is a leading cause of cancer-related deaths worldwide. Here, we assessed the chemotherapeutic effect of grape seed proanthocyanidins (GSPs) on human non-small cell lung cancer (NSCLC) cells in vitro and in vivo using a tumor xenograft model. Experimental Design: The effects of G...

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Veröffentlicht in:Clinical cancer research 2009-02, Vol.15 (3), p.821-831
Hauptverfasser: Akhtar, Suhail, Meeran, Syed M, Katiyar, Nandan, Katiyar, Santosh K
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creator Akhtar, Suhail
Meeran, Syed M
Katiyar, Nandan
Katiyar, Santosh K
description Purpose: Lung cancer is a leading cause of cancer-related deaths worldwide. Here, we assessed the chemotherapeutic effect of grape seed proanthocyanidins (GSPs) on human non-small cell lung cancer (NSCLC) cells in vitro and in vivo using a tumor xenograft model. Experimental Design: The effects of GSPs on human NSCLC cell lines in terms of cellular proliferation were determined. The chemotherapeutic effects of a GSP- supplemented AIN76A control diet fed to nude mice bearing tumor xenografts (A549 and H1299) were evaluated in terms of biomarkers of cell proliferation and angiogenesis and on insulin-like growth factor binding protein-3 using immunohistochemical detection, ELISA, and Western blotting. Results: In vitro treatment of NSCLC cells with GSPs resulted in inhibition of cellular proliferation. Administration of GSPs (0.1%, 0.2%, and 0.5%, w/w) as a supplement of an AIN76A control diet resulted in a dose-dependent inhibition of the growth of NSCLC (A549 and H1299) tumor xenografts in athymic nude mice (25-76%; P < 0.05-0.001). The growth-inhibitory effect of GSPs on the NSCLC xenograft tumors was associated with the enhancement of the levels of insulin-like growth factor binding protein-3 in the tumor microenvironment and plasma and antiproliferative, antiangiogenic, and proapoptotic effects. Conclusions: This preclinical study reveals for the first time that dietary GSPs have the ability to inhibit the growth of human NSCLC tumor xenografts grown in vivo in athymic nude mice. More studies are needed to develop GSPs as a pharmacologically safe agent for the prevention of lung cancer in humans.
doi_str_mv 10.1158/1078-0432.CCR-08-1901
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Here, we assessed the chemotherapeutic effect of grape seed proanthocyanidins (GSPs) on human non-small cell lung cancer (NSCLC) cells in vitro and in vivo using a tumor xenograft model. Experimental Design: The effects of GSPs on human NSCLC cell lines in terms of cellular proliferation were determined. The chemotherapeutic effects of a GSP- supplemented AIN76A control diet fed to nude mice bearing tumor xenografts (A549 and H1299) were evaluated in terms of biomarkers of cell proliferation and angiogenesis and on insulin-like growth factor binding protein-3 using immunohistochemical detection, ELISA, and Western blotting. Results: In vitro treatment of NSCLC cells with GSPs resulted in inhibition of cellular proliferation. Administration of GSPs (0.1%, 0.2%, and 0.5%, w/w) as a supplement of an AIN76A control diet resulted in a dose-dependent inhibition of the growth of NSCLC (A549 and H1299) tumor xenografts in athymic nude mice (25-76%; P &lt; 0.05-0.001). The growth-inhibitory effect of GSPs on the NSCLC xenograft tumors was associated with the enhancement of the levels of insulin-like growth factor binding protein-3 in the tumor microenvironment and plasma and antiproliferative, antiangiogenic, and proapoptotic effects. Conclusions: This preclinical study reveals for the first time that dietary GSPs have the ability to inhibit the growth of human NSCLC tumor xenografts grown in vivo in athymic nude mice. More studies are needed to develop GSPs as a pharmacologically safe agent for the prevention of lung cancer in humans.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-08-1901</identifier><identifier>PMID: 19188152</identifier><language>eng</language><publisher>United States: American Association for Cancer Research</publisher><subject>angiogenesis ; Angiogenesis Inducing Agents - antagonists &amp; inhibitors ; Animals ; Apoptosis - drug effects ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Diet ; Grape Seed Extract ; grape seed proanthocyanidins ; Humans ; Insulin-Like Growth Factor Binding Protein 3 - metabolism ; Insulin-Like Growth Factor Binding Protein 3 - physiology ; Lung Neoplasms - drug therapy ; Mice ; Mice, Nude ; non-small cell human lung cancer ; Plant Extracts - administration &amp; dosage ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Proanthocyanidins - administration &amp; dosage ; Proanthocyanidins - pharmacology ; Proanthocyanidins - therapeutic use ; tumor cell proliferation ; tumor xenograft ; Xenograft Model Antitumor Assays</subject><ispartof>Clinical cancer research, 2009-02, Vol.15 (3), p.821-831</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-7d0ccd8a4ece4b43dc7725cc4d14bb90cb132b9b6e4bece756353c98550b3dc13</citedby><cites>FETCH-LOGICAL-c386t-7d0ccd8a4ece4b43dc7725cc4d14bb90cb132b9b6e4bece756353c98550b3dc13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3343,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19188152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akhtar, Suhail</creatorcontrib><creatorcontrib>Meeran, Syed M</creatorcontrib><creatorcontrib>Katiyar, Nandan</creatorcontrib><creatorcontrib>Katiyar, Santosh K</creatorcontrib><title>Grape Seed Proanthocyanidins Inhibit the Growth of Human Non-Small Cell Lung Cancer Xenografts by Targeting Insulin-Like Growth Factor Binding Protein-3, Tumor Cell Proliferation, and Angiogenic Factors</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Purpose: Lung cancer is a leading cause of cancer-related deaths worldwide. Here, we assessed the chemotherapeutic effect of grape seed proanthocyanidins (GSPs) on human non-small cell lung cancer (NSCLC) cells in vitro and in vivo using a tumor xenograft model. Experimental Design: The effects of GSPs on human NSCLC cell lines in terms of cellular proliferation were determined. The chemotherapeutic effects of a GSP- supplemented AIN76A control diet fed to nude mice bearing tumor xenografts (A549 and H1299) were evaluated in terms of biomarkers of cell proliferation and angiogenesis and on insulin-like growth factor binding protein-3 using immunohistochemical detection, ELISA, and Western blotting. Results: In vitro treatment of NSCLC cells with GSPs resulted in inhibition of cellular proliferation. Administration of GSPs (0.1%, 0.2%, and 0.5%, w/w) as a supplement of an AIN76A control diet resulted in a dose-dependent inhibition of the growth of NSCLC (A549 and H1299) tumor xenografts in athymic nude mice (25-76%; P &lt; 0.05-0.001). The growth-inhibitory effect of GSPs on the NSCLC xenograft tumors was associated with the enhancement of the levels of insulin-like growth factor binding protein-3 in the tumor microenvironment and plasma and antiproliferative, antiangiogenic, and proapoptotic effects. Conclusions: This preclinical study reveals for the first time that dietary GSPs have the ability to inhibit the growth of human NSCLC tumor xenografts grown in vivo in athymic nude mice. More studies are needed to develop GSPs as a pharmacologically safe agent for the prevention of lung cancer in humans.</description><subject>angiogenesis</subject><subject>Angiogenesis Inducing Agents - antagonists &amp; inhibitors</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Diet</subject><subject>Grape Seed Extract</subject><subject>grape seed proanthocyanidins</subject><subject>Humans</subject><subject>Insulin-Like Growth Factor Binding Protein 3 - metabolism</subject><subject>Insulin-Like Growth Factor Binding Protein 3 - physiology</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>non-small cell human lung cancer</subject><subject>Plant Extracts - administration &amp; dosage</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Proanthocyanidins - administration &amp; dosage</subject><subject>Proanthocyanidins - pharmacology</subject><subject>Proanthocyanidins - therapeutic use</subject><subject>tumor cell proliferation</subject><subject>tumor xenograft</subject><subject>Xenograft Model Antitumor Assays</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkcFu1DAQhiMEoqXwCCCf4NIUO44T77FEdLvSChBdJG6W7UwSQ2IvtqNqX5GnqtPdwsW25v_mn5H_LHtL8BUhjH8kuOY5Lmlx1TTfc8xzssLkWXZOGKtzWlTseXo_MWfZqxB-YUxKgsuX2RlZEc4JK86zv2sv94DuAFr0zTtp4-D0QVrTGhvQxg5GmYjiAGjt3X0ckOvQ7TxJi744m99NchxRA-nYzrZHjbQaPPoJ1vVedjEgdUA76XuIJskbG-bR2Hxrfv_zu5E6Oo8-GdsuSNohQkLoJdrNUxIezVN1NB14GY2zl0jaFl3b3rgerNEni_A6e9HJMcCb032R_bj5vGtu8-3X9aa53uaa8irmdYu1brksQUOpStrqui6Y1mVLSqVWWCtCC7VSVVITUrOKMqpXnDGsEkzoRfb-6Lv37s8MIYrJBJ3WlBbcHERVcY55uYDsCGrvQvDQib03k_QHQbBYQhRLQGIJSKQQBU6FFGLqe3caMKsJ2v9dp9QS8OEIDKYf7o0HoR8_3kMA6fUgCBNU8ILQB9fcqaU</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Akhtar, Suhail</creator><creator>Meeran, Syed M</creator><creator>Katiyar, Nandan</creator><creator>Katiyar, Santosh K</creator><general>American Association for Cancer Research</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>7X8</scope></search><sort><creationdate>20090201</creationdate><title>Grape Seed Proanthocyanidins Inhibit the Growth of Human Non-Small Cell Lung Cancer Xenografts by Targeting Insulin-Like Growth Factor Binding Protein-3, Tumor Cell Proliferation, and Angiogenic Factors</title><author>Akhtar, Suhail ; Meeran, Syed M ; Katiyar, Nandan ; Katiyar, Santosh K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-7d0ccd8a4ece4b43dc7725cc4d14bb90cb132b9b6e4bece756353c98550b3dc13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>angiogenesis</topic><topic>Angiogenesis Inducing Agents - antagonists &amp; inhibitors</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Diet</topic><topic>Grape Seed Extract</topic><topic>grape seed proanthocyanidins</topic><topic>Humans</topic><topic>Insulin-Like Growth Factor Binding Protein 3 - metabolism</topic><topic>Insulin-Like Growth Factor Binding Protein 3 - physiology</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>non-small cell human lung cancer</topic><topic>Plant Extracts - administration &amp; dosage</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>Proanthocyanidins - administration &amp; dosage</topic><topic>Proanthocyanidins - pharmacology</topic><topic>Proanthocyanidins - therapeutic use</topic><topic>tumor cell proliferation</topic><topic>tumor xenograft</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akhtar, Suhail</creatorcontrib><creatorcontrib>Meeran, Syed M</creatorcontrib><creatorcontrib>Katiyar, Nandan</creatorcontrib><creatorcontrib>Katiyar, Santosh K</creatorcontrib><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>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akhtar, Suhail</au><au>Meeran, Syed M</au><au>Katiyar, Nandan</au><au>Katiyar, Santosh K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Grape Seed Proanthocyanidins Inhibit the Growth of Human Non-Small Cell Lung Cancer Xenografts by Targeting Insulin-Like Growth Factor Binding Protein-3, Tumor Cell Proliferation, and Angiogenic Factors</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>15</volume><issue>3</issue><spage>821</spage><epage>831</epage><pages>821-831</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Purpose: Lung cancer is a leading cause of cancer-related deaths worldwide. Here, we assessed the chemotherapeutic effect of grape seed proanthocyanidins (GSPs) on human non-small cell lung cancer (NSCLC) cells in vitro and in vivo using a tumor xenograft model. Experimental Design: The effects of GSPs on human NSCLC cell lines in terms of cellular proliferation were determined. The chemotherapeutic effects of a GSP- supplemented AIN76A control diet fed to nude mice bearing tumor xenografts (A549 and H1299) were evaluated in terms of biomarkers of cell proliferation and angiogenesis and on insulin-like growth factor binding protein-3 using immunohistochemical detection, ELISA, and Western blotting. Results: In vitro treatment of NSCLC cells with GSPs resulted in inhibition of cellular proliferation. Administration of GSPs (0.1%, 0.2%, and 0.5%, w/w) as a supplement of an AIN76A control diet resulted in a dose-dependent inhibition of the growth of NSCLC (A549 and H1299) tumor xenografts in athymic nude mice (25-76%; P &lt; 0.05-0.001). The growth-inhibitory effect of GSPs on the NSCLC xenograft tumors was associated with the enhancement of the levels of insulin-like growth factor binding protein-3 in the tumor microenvironment and plasma and antiproliferative, antiangiogenic, and proapoptotic effects. Conclusions: This preclinical study reveals for the first time that dietary GSPs have the ability to inhibit the growth of human NSCLC tumor xenografts grown in vivo in athymic nude mice. More studies are needed to develop GSPs as a pharmacologically safe agent for the prevention of lung cancer in humans.</abstract><cop>United States</cop><pub>American Association for Cancer Research</pub><pmid>19188152</pmid><doi>10.1158/1078-0432.CCR-08-1901</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects angiogenesis
Angiogenesis Inducing Agents - antagonists & inhibitors
Animals
Apoptosis - drug effects
Carcinoma, Non-Small-Cell Lung - drug therapy
Cell Line, Tumor
Cell Proliferation - drug effects
Diet
Grape Seed Extract
grape seed proanthocyanidins
Humans
Insulin-Like Growth Factor Binding Protein 3 - metabolism
Insulin-Like Growth Factor Binding Protein 3 - physiology
Lung Neoplasms - drug therapy
Mice
Mice, Nude
non-small cell human lung cancer
Plant Extracts - administration & dosage
Plant Extracts - pharmacology
Plant Extracts - therapeutic use
Proanthocyanidins - administration & dosage
Proanthocyanidins - pharmacology
Proanthocyanidins - therapeutic use
tumor cell proliferation
tumor xenograft
Xenograft Model Antitumor Assays
title Grape Seed Proanthocyanidins Inhibit the Growth of Human Non-Small Cell Lung Cancer Xenografts by Targeting Insulin-Like Growth Factor Binding Protein-3, Tumor Cell Proliferation, and Angiogenic Factors
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