Efficacy of Dietary Antioxidants Combined with a Chemotherapeutic Agent on Human Colon Cancer Progression in a Fluorescent Orthotopic Mouse Model
We report here the efficacy of dietary antioxidants in combination with chemotherapy on tumor growth in the orthotopic COLO-205-green fluorescent protein (GFP) human colon cancer mouse model. The orthotopically-transplanted nude mice used for the study were randomly divided into 5 groups (A-E) after...
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creator | Ma, Huaiyu Das, Tapas Pereira, Suzette Yang, Zhijian Zhao, Ming Mukerji, Pradip Hoffman, Robert M |
description | We report here the efficacy of dietary antioxidants in combination with chemotherapy on tumor growth in the orthotopic COLO-205-green
fluorescent protein (GFP) human colon cancer mouse model. The orthotopically-transplanted nude mice used for the study were
randomly divided into 5 groups (A-E) after surgical orthotopic implantation (SOI) of tumor tissue. The following diets were
given: Diet A, modified AIN-93M mature rodent diet with 4% fish oil; Diet B, modified AIN-93M which contains added antioxidants
vitamin A, vitamin E, and selenium at levels present in the standard AIN-93M diet; Diet C, Diet A without added antioxidants
vitamin A, vitamin E, or selenium; Diet D, Diet A with 5 times the amount of added antioxidants vitamin A, vitamin E, and
selenium present in Diet B. Cisplatin, 7 mg/kg, was administered intraperitoneally on day 16 after SOI. Throughout the course
of treatment, noninvasive whole-body imaging, based on the GFP expression of the tumor, permitted visualization of tumor progression.
At sacrifice, the mean tumor weights showed significant statistical differences in all of the treated groups compared to the
negative control (no cisplatin treatment) (pâ¤0.001). The mean tumor weight showed a significant statistical difference between
the Diet D combined with the cisplatin group compared to Diet B combined with cisplatin (p=0.038). Thus, we have demonstrated
that Diet D is effective against tumor growth in combination with cisplatin in the fluorescent mouse model of colon cancer
COLO-205 GFP. The results of the present study therefore indicate enhancement of cisplatin efficacy by high-dose antioxidants
in combination with fish oil for colon cancer progression and suggests the design of clinical trials for this regimen. |
format | Article |
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fluorescent protein (GFP) human colon cancer mouse model. The orthotopically-transplanted nude mice used for the study were
randomly divided into 5 groups (A-E) after surgical orthotopic implantation (SOI) of tumor tissue. The following diets were
given: Diet A, modified AIN-93M mature rodent diet with 4% fish oil; Diet B, modified AIN-93M which contains added antioxidants
vitamin A, vitamin E, and selenium at levels present in the standard AIN-93M diet; Diet C, Diet A without added antioxidants
vitamin A, vitamin E, or selenium; Diet D, Diet A with 5 times the amount of added antioxidants vitamin A, vitamin E, and
selenium present in Diet B. Cisplatin, 7 mg/kg, was administered intraperitoneally on day 16 after SOI. Throughout the course
of treatment, noninvasive whole-body imaging, based on the GFP expression of the tumor, permitted visualization of tumor progression.
At sacrifice, the mean tumor weights showed significant statistical differences in all of the treated groups compared to the
negative control (no cisplatin treatment) (pâ¤0.001). The mean tumor weight showed a significant statistical difference between
the Diet D combined with the cisplatin group compared to Diet B combined with cisplatin (p=0.038). Thus, we have demonstrated
that Diet D is effective against tumor growth in combination with cisplatin in the fluorescent mouse model of colon cancer
COLO-205 GFP. The results of the present study therefore indicate enhancement of cisplatin efficacy by high-dose antioxidants
in combination with fish oil for colon cancer progression and suggests the design of clinical trials for this regimen.</description><identifier>ISSN: 0250-7005</identifier><identifier>EISSN: 1791-7530</identifier><identifier>PMID: 19596909</identifier><language>eng</language><publisher>Attiki: International Institute of Anticancer Research</publisher><subject>Animals ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - therapeutic use ; Antioxidants - administration & dosage ; Antioxidants - therapeutic use ; Biological and medical sciences ; Body Weight ; Cell Line ; Colonic Neoplasms - drug therapy ; Colonic Neoplasms - pathology ; Dietary Supplements ; Disease Models, Animal ; Disease Progression ; Feeding Behavior ; Female ; Fluorescence ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Male ; Medical sciences ; Mice ; Mice, Nude ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Anticancer research, 2009-07, Vol.29 (7), p.2421-2426</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21713464$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19596909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Huaiyu</creatorcontrib><creatorcontrib>Das, Tapas</creatorcontrib><creatorcontrib>Pereira, Suzette</creatorcontrib><creatorcontrib>Yang, Zhijian</creatorcontrib><creatorcontrib>Zhao, Ming</creatorcontrib><creatorcontrib>Mukerji, Pradip</creatorcontrib><creatorcontrib>Hoffman, Robert M</creatorcontrib><title>Efficacy of Dietary Antioxidants Combined with a Chemotherapeutic Agent on Human Colon Cancer Progression in a Fluorescent Orthotopic Mouse Model</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><description>We report here the efficacy of dietary antioxidants in combination with chemotherapy on tumor growth in the orthotopic COLO-205-green
fluorescent protein (GFP) human colon cancer mouse model. The orthotopically-transplanted nude mice used for the study were
randomly divided into 5 groups (A-E) after surgical orthotopic implantation (SOI) of tumor tissue. The following diets were
given: Diet A, modified AIN-93M mature rodent diet with 4% fish oil; Diet B, modified AIN-93M which contains added antioxidants
vitamin A, vitamin E, and selenium at levels present in the standard AIN-93M diet; Diet C, Diet A without added antioxidants
vitamin A, vitamin E, or selenium; Diet D, Diet A with 5 times the amount of added antioxidants vitamin A, vitamin E, and
selenium present in Diet B. Cisplatin, 7 mg/kg, was administered intraperitoneally on day 16 after SOI. Throughout the course
of treatment, noninvasive whole-body imaging, based on the GFP expression of the tumor, permitted visualization of tumor progression.
At sacrifice, the mean tumor weights showed significant statistical differences in all of the treated groups compared to the
negative control (no cisplatin treatment) (pâ¤0.001). The mean tumor weight showed a significant statistical difference between
the Diet D combined with the cisplatin group compared to Diet B combined with cisplatin (p=0.038). Thus, we have demonstrated
that Diet D is effective against tumor growth in combination with cisplatin in the fluorescent mouse model of colon cancer
COLO-205 GFP. The results of the present study therefore indicate enhancement of cisplatin efficacy by high-dose antioxidants
in combination with fish oil for colon cancer progression and suggests the design of clinical trials for this regimen.</description><subject>Animals</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Antioxidants - administration & dosage</subject><subject>Antioxidants - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Body Weight</subject><subject>Cell Line</subject><subject>Colonic Neoplasms - drug therapy</subject><subject>Colonic Neoplasms - pathology</subject><subject>Dietary Supplements</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Feeding Behavior</subject><subject>Female</subject><subject>Fluorescence</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0250-7005</issn><issn>1791-7530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM1O3TAQhSNUBLfAK1TetLtIdhzb8fIq5U8C0UVZR44zvjFy7FvbEeUxeGOMuC2bmdHRN0dn5qjaECFJLRjFX6oNbhiuBcbstPqa0hPGnMuOnlSnRDLJJZab6vXSGKuVfkHBoJ8WsoovaOuzDX_tpHxOqA_LaD1M6NnmGSnUz7CEPENUe1iz1Wi7A59R8OhmXZQvvCtzr7yGiH7FsIuQki2S9WX7yq2hCPp95SHmOeSwLx73YU1Q6gTuvDo2yiW4OPSz6vHq8nd_U989XN_227t6brjMNQHGmdYwGsY4Hbup7YwgbQPANW35KBUeNR8VFZIrZjpJG9ZNVBKDodOg6Fn148N3H8OfFVIeFltyOac8lDQDF63grMUF_HYA13GBadhHu5QvDf-eWIDvB0AlrZyJ5Xab_nMNEaQkaj-52e7mZxthSItyrtjSQcVGDmJo2obQNxCWivY</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Ma, Huaiyu</creator><creator>Das, Tapas</creator><creator>Pereira, Suzette</creator><creator>Yang, Zhijian</creator><creator>Zhao, Ming</creator><creator>Mukerji, Pradip</creator><creator>Hoffman, Robert M</creator><general>International Institute of Anticancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20090701</creationdate><title>Efficacy of Dietary Antioxidants Combined with a Chemotherapeutic Agent on Human Colon Cancer Progression in a Fluorescent Orthotopic Mouse Model</title><author>Ma, Huaiyu ; Das, Tapas ; Pereira, Suzette ; Yang, Zhijian ; Zhao, Ming ; Mukerji, Pradip ; Hoffman, Robert M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h269t-1e565ccebf5563b8d48f7142ee6c346b9a0bc6ba3796a5f893258d391f0e8cea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Antioxidants - administration & dosage</topic><topic>Antioxidants - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Body Weight</topic><topic>Cell Line</topic><topic>Colonic Neoplasms - drug therapy</topic><topic>Colonic Neoplasms - pathology</topic><topic>Dietary Supplements</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Feeding Behavior</topic><topic>Female</topic><topic>Fluorescence</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Huaiyu</creatorcontrib><creatorcontrib>Das, Tapas</creatorcontrib><creatorcontrib>Pereira, Suzette</creatorcontrib><creatorcontrib>Yang, Zhijian</creatorcontrib><creatorcontrib>Zhao, Ming</creatorcontrib><creatorcontrib>Mukerji, Pradip</creatorcontrib><creatorcontrib>Hoffman, Robert M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Anticancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Huaiyu</au><au>Das, Tapas</au><au>Pereira, Suzette</au><au>Yang, Zhijian</au><au>Zhao, Ming</au><au>Mukerji, Pradip</au><au>Hoffman, Robert M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of Dietary Antioxidants Combined with a Chemotherapeutic Agent on Human Colon Cancer Progression in a Fluorescent Orthotopic Mouse Model</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2009-07-01</date><risdate>2009</risdate><volume>29</volume><issue>7</issue><spage>2421</spage><epage>2426</epage><pages>2421-2426</pages><issn>0250-7005</issn><eissn>1791-7530</eissn><abstract>We report here the efficacy of dietary antioxidants in combination with chemotherapy on tumor growth in the orthotopic COLO-205-green
fluorescent protein (GFP) human colon cancer mouse model. The orthotopically-transplanted nude mice used for the study were
randomly divided into 5 groups (A-E) after surgical orthotopic implantation (SOI) of tumor tissue. The following diets were
given: Diet A, modified AIN-93M mature rodent diet with 4% fish oil; Diet B, modified AIN-93M which contains added antioxidants
vitamin A, vitamin E, and selenium at levels present in the standard AIN-93M diet; Diet C, Diet A without added antioxidants
vitamin A, vitamin E, or selenium; Diet D, Diet A with 5 times the amount of added antioxidants vitamin A, vitamin E, and
selenium present in Diet B. Cisplatin, 7 mg/kg, was administered intraperitoneally on day 16 after SOI. Throughout the course
of treatment, noninvasive whole-body imaging, based on the GFP expression of the tumor, permitted visualization of tumor progression.
At sacrifice, the mean tumor weights showed significant statistical differences in all of the treated groups compared to the
negative control (no cisplatin treatment) (pâ¤0.001). The mean tumor weight showed a significant statistical difference between
the Diet D combined with the cisplatin group compared to Diet B combined with cisplatin (p=0.038). Thus, we have demonstrated
that Diet D is effective against tumor growth in combination with cisplatin in the fluorescent mouse model of colon cancer
COLO-205 GFP. The results of the present study therefore indicate enhancement of cisplatin efficacy by high-dose antioxidants
in combination with fish oil for colon cancer progression and suggests the design of clinical trials for this regimen.</abstract><cop>Attiki</cop><pub>International Institute of Anticancer Research</pub><pmid>19596909</pmid><tpages>6</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Antineoplastic Agents - administration & dosage Antineoplastic Agents - therapeutic use Antioxidants - administration & dosage Antioxidants - therapeutic use Biological and medical sciences Body Weight Cell Line Colonic Neoplasms - drug therapy Colonic Neoplasms - pathology Dietary Supplements Disease Models, Animal Disease Progression Feeding Behavior Female Fluorescence Gastroenterology. Liver. Pancreas. Abdomen Humans Male Medical sciences Mice Mice, Nude Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Efficacy of Dietary Antioxidants Combined with a Chemotherapeutic Agent on Human Colon Cancer Progression in a Fluorescent Orthotopic Mouse Model |
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