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Treatment of Meningeal Breast Cancer Xenografts in the Rat Using an Anti-P185/HER2 Antibody
The metastatic spread of breast cancer to the leptomeninges (LM) is a painful, debilitating, and usually lethal condition. Current therapies are generally ineffective or extremely toxic. The current study evaluated monoclonal antibody therapy in an animal model of LM human breast cancer. Monoclonal...
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Published in: | Clinical cancer research 2001-07, Vol.7 (7), p.2050-2056 |
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creator | BERGMAN, Ira BARMADA, Mamdouha A GRIFFIN, Judith A SLAMON, Dennis J |
description | The metastatic spread of breast cancer to the leptomeninges (LM) is a painful, debilitating, and usually lethal condition.
Current therapies are generally ineffective or extremely toxic. The current study evaluated monoclonal antibody therapy in
an animal model of LM human breast cancer. Monoclonal antibody 4D5, which recognizes the extracellular domain of the HER2/neu
receptor, was administered into the cerebrospinal fluid of athymic rats implanted with human breast cancer cell lines. Continuous
intraventricular administration of 4D5 inhibited growth of SKBR3 cells that overexpress HER2/neu but not of MCF7 cells, which do not. Inhibition was dose-dependent, with higher doses of 4D5 producing an improved response.
i.p. administration of cisplatin in addition to 4D5 did not improve results. Continuous administration of 4D5 into the lumbar,
as opposed to the ventricular intrathecal space, was not therapeutically effective. Treatment with 4D5 did not result in outgrowth
of cells lacking expression of the HER2/neu receptor. These results suggest that 4D5, administered regionally, may palliate
LM metastases from HER2/neu -overexpressing breast carcinoma. |
format | article |
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Current therapies are generally ineffective or extremely toxic. The current study evaluated monoclonal antibody therapy in
an animal model of LM human breast cancer. Monoclonal antibody 4D5, which recognizes the extracellular domain of the HER2/neu
receptor, was administered into the cerebrospinal fluid of athymic rats implanted with human breast cancer cell lines. Continuous
intraventricular administration of 4D5 inhibited growth of SKBR3 cells that overexpress HER2/neu but not of MCF7 cells, which do not. Inhibition was dose-dependent, with higher doses of 4D5 producing an improved response.
i.p. administration of cisplatin in addition to 4D5 did not improve results. Continuous administration of 4D5 into the lumbar,
as opposed to the ventricular intrathecal space, was not therapeutically effective. Treatment with 4D5 did not result in outgrowth
of cells lacking expression of the HER2/neu receptor. These results suggest that 4D5, administered regionally, may palliate
LM metastases from HER2/neu -overexpressing breast carcinoma.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>PMID: 11448923</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Animals ; Antibodies, Monoclonal - cerebrospinal fluid ; Antibodies, Monoclonal - pharmacology ; Antibodies, Monoclonal - therapeutic use ; Antineoplastic agents ; Biological and medical sciences ; Brain - drug effects ; Brain - immunology ; Brain - pathology ; Breast Neoplasms - drug therapy ; Breast Neoplasms - immunology ; Breast Neoplasms - pathology ; Cell Division - drug effects ; Dose-Response Relationship, Drug ; Female ; Humans ; Immunohistochemistry ; Immunotherapy ; Injections, Intraventricular ; Medical sciences ; Meningeal Neoplasms - drug therapy ; Meningeal Neoplasms - secondary ; Neoplasm Transplantation ; Pharmacology. Drug treatments ; Rats ; Rats, Nude ; Receptor, ErbB-2 - immunology ; Receptor, ErbB-2 - metabolism ; Tumor Cells, Cultured ; Xenograft Model Antitumor Assays</subject><ispartof>Clinical cancer research, 2001-07, Vol.7 (7), p.2050-2056</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1083286$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11448923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BERGMAN, Ira</creatorcontrib><creatorcontrib>BARMADA, Mamdouha A</creatorcontrib><creatorcontrib>GRIFFIN, Judith A</creatorcontrib><creatorcontrib>SLAMON, Dennis J</creatorcontrib><title>Treatment of Meningeal Breast Cancer Xenografts in the Rat Using an Anti-P185/HER2 Antibody</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>The metastatic spread of breast cancer to the leptomeninges (LM) is a painful, debilitating, and usually lethal condition.
Current therapies are generally ineffective or extremely toxic. The current study evaluated monoclonal antibody therapy in
an animal model of LM human breast cancer. Monoclonal antibody 4D5, which recognizes the extracellular domain of the HER2/neu
receptor, was administered into the cerebrospinal fluid of athymic rats implanted with human breast cancer cell lines. Continuous
intraventricular administration of 4D5 inhibited growth of SKBR3 cells that overexpress HER2/neu but not of MCF7 cells, which do not. Inhibition was dose-dependent, with higher doses of 4D5 producing an improved response.
i.p. administration of cisplatin in addition to 4D5 did not improve results. Continuous administration of 4D5 into the lumbar,
as opposed to the ventricular intrathecal space, was not therapeutically effective. Treatment with 4D5 did not result in outgrowth
of cells lacking expression of the HER2/neu receptor. These results suggest that 4D5, administered regionally, may palliate
LM metastases from HER2/neu -overexpressing breast carcinoma.</description><subject>Animals</subject><subject>Antibodies, Monoclonal - cerebrospinal fluid</subject><subject>Antibodies, Monoclonal - pharmacology</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Brain - drug effects</subject><subject>Brain - immunology</subject><subject>Brain - pathology</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - immunology</subject><subject>Breast Neoplasms - pathology</subject><subject>Cell Division - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Immunotherapy</subject><subject>Injections, Intraventricular</subject><subject>Medical sciences</subject><subject>Meningeal Neoplasms - drug therapy</subject><subject>Meningeal Neoplasms - secondary</subject><subject>Neoplasm Transplantation</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Nude</subject><subject>Receptor, ErbB-2 - immunology</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Tumor Cells, Cultured</subject><subject>Xenograft Model Antitumor Assays</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpFz01LAzEQBuBFFFurf0FyEDwt5ms36bGWaoWKUloQPCyzm0l3pU1LEpH-e0NbkTnMBw8D71nWZ0WhcsHL4jzNVOmcSsF72VUIX5Qyyai8zHqMSamHXPSzz4VHiBt0kWwteUXXuRXCmjymc4hkDK5BTz7QbVcebAykcyS2SOYQyTIkTMCRkYtd_s508TCdzPlhrbdmf51dWFgHvDn1QbZ8mizG03z29vwyHs3ylpc65owrsHYodKMKbep6WGrNlOC21NyAsMagkYxTKJXhzFKJ1DbK8hoLDhRBDLLb49_dd71BU-18twG_r_5SJnB3AhAaWFufUnXh31EtuC4Tuz-ytlu1P53HqjnE9xgQfNNWKhWnBRW_8r5ocA</recordid><startdate>20010701</startdate><enddate>20010701</enddate><creator>BERGMAN, Ira</creator><creator>BARMADA, Mamdouha A</creator><creator>GRIFFIN, Judith A</creator><creator>SLAMON, Dennis J</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20010701</creationdate><title>Treatment of Meningeal Breast Cancer Xenografts in the Rat Using an Anti-P185/HER2 Antibody</title><author>BERGMAN, Ira ; BARMADA, Mamdouha A ; GRIFFIN, Judith A ; SLAMON, Dennis J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h268t-127aff938c758dbb96881732f682da3fdded4120a67d21f04e0fc7f2be52a0ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal - cerebrospinal fluid</topic><topic>Antibodies, Monoclonal - pharmacology</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Brain - drug effects</topic><topic>Brain - immunology</topic><topic>Brain - pathology</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - immunology</topic><topic>Breast Neoplasms - pathology</topic><topic>Cell Division - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunotherapy</topic><topic>Injections, Intraventricular</topic><topic>Medical sciences</topic><topic>Meningeal Neoplasms - drug therapy</topic><topic>Meningeal Neoplasms - secondary</topic><topic>Neoplasm Transplantation</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Nude</topic><topic>Receptor, ErbB-2 - immunology</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Tumor Cells, Cultured</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BERGMAN, Ira</creatorcontrib><creatorcontrib>BARMADA, Mamdouha A</creatorcontrib><creatorcontrib>GRIFFIN, Judith A</creatorcontrib><creatorcontrib>SLAMON, Dennis J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BERGMAN, Ira</au><au>BARMADA, Mamdouha A</au><au>GRIFFIN, Judith A</au><au>SLAMON, Dennis J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of Meningeal Breast Cancer Xenografts in the Rat Using an Anti-P185/HER2 Antibody</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2001-07-01</date><risdate>2001</risdate><volume>7</volume><issue>7</issue><spage>2050</spage><epage>2056</epage><pages>2050-2056</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>The metastatic spread of breast cancer to the leptomeninges (LM) is a painful, debilitating, and usually lethal condition.
Current therapies are generally ineffective or extremely toxic. The current study evaluated monoclonal antibody therapy in
an animal model of LM human breast cancer. Monoclonal antibody 4D5, which recognizes the extracellular domain of the HER2/neu
receptor, was administered into the cerebrospinal fluid of athymic rats implanted with human breast cancer cell lines. Continuous
intraventricular administration of 4D5 inhibited growth of SKBR3 cells that overexpress HER2/neu but not of MCF7 cells, which do not. Inhibition was dose-dependent, with higher doses of 4D5 producing an improved response.
i.p. administration of cisplatin in addition to 4D5 did not improve results. Continuous administration of 4D5 into the lumbar,
as opposed to the ventricular intrathecal space, was not therapeutically effective. Treatment with 4D5 did not result in outgrowth
of cells lacking expression of the HER2/neu receptor. These results suggest that 4D5, administered regionally, may palliate
LM metastases from HER2/neu -overexpressing breast carcinoma.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>11448923</pmid><tpages>7</tpages></addata></record> |
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subjects | Animals Antibodies, Monoclonal - cerebrospinal fluid Antibodies, Monoclonal - pharmacology Antibodies, Monoclonal - therapeutic use Antineoplastic agents Biological and medical sciences Brain - drug effects Brain - immunology Brain - pathology Breast Neoplasms - drug therapy Breast Neoplasms - immunology Breast Neoplasms - pathology Cell Division - drug effects Dose-Response Relationship, Drug Female Humans Immunohistochemistry Immunotherapy Injections, Intraventricular Medical sciences Meningeal Neoplasms - drug therapy Meningeal Neoplasms - secondary Neoplasm Transplantation Pharmacology. Drug treatments Rats Rats, Nude Receptor, ErbB-2 - immunology Receptor, ErbB-2 - metabolism Tumor Cells, Cultured Xenograft Model Antitumor Assays |
title | Treatment of Meningeal Breast Cancer Xenografts in the Rat Using an Anti-P185/HER2 Antibody |
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