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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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 |
format | Article |
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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.</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 & 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</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 < 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 & 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 & dosage</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Proanthocyanidins - administration & 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 & 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 & dosage</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>Proanthocyanidins - administration & 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 < 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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