Source:http://linkedlifedata.com/resource/pubmed/id/16398612
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2006-1-9
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pubmed:abstractText |
The members of the epidermal growth factor receptor (EGFR) family are over expressed in a variety of malignancies and are frequently linked to aggressive disease and a poor prognosis. Although clinically effective monoclonal antibodies (MAbs) have been developed to target HER2 and EGFR, the remaining two family members, HER3 and HER4, have not been the subject of significant efforts. In this paper, we have taken the initial steps required to generate antibodies with potential clinically utility that target the members of the EGFR family. The genes for the extracellular domains (ECDs) of all four members of the EGFR family were cloned and used to stably transfect 293 (HEK) cells. Milligram quantities of each ECD were produced and characterized. The HER3, HER4, and EGFR ECDs were then employed as targets for the selection of antibodies from naïve human scFv (single-chain Fv) phage display libraries. Six unique scFv clones were isolated that bound specifically to HER3, 13 unique clones were isolated with specificity for HER4 and 52 unique anti-EGFR clones were isolated. These scFvs provide a valuable and potentially clinically relevant panel of agents to target the members of the EGFR family.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Variable Region,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/receptor tyrosine-protein kinase...
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1084-9785
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pubmed:author |
pubmed-author:AdamsGregory PGP,
pubmed-author:FurmanovaPolinaP,
pubmed-author:GarrisonJenniferJ,
pubmed-author:HeitnerTaraT,
pubmed-author:HorakEvaE,
pubmed-author:LouJianlongJ,
pubmed-author:MarksJames DJD,
pubmed-author:RobinsonMatthew KMK,
pubmed-author:RussevaMariaM,
pubmed-author:SimmonsHeidi HHH,
pubmed-author:WeinerLouis MLM,
pubmed-author:YuZhouZ,
pubmed-author:YuanQing-AnQA
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pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
603-13
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pubmed:dateRevised |
2011-11-2
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pubmed:meshHeading |
pubmed-meshheading:16398612-Base Sequence,
pubmed-meshheading:16398612-Cell Line,
pubmed-meshheading:16398612-Cell Line, Tumor,
pubmed-meshheading:16398612-Cloning, Molecular,
pubmed-meshheading:16398612-DNA Primers,
pubmed-meshheading:16398612-Female,
pubmed-meshheading:16398612-Humans,
pubmed-meshheading:16398612-Immunoglobulin Variable Region,
pubmed-meshheading:16398612-Kidney,
pubmed-meshheading:16398612-Molecular Sequence Data,
pubmed-meshheading:16398612-Ovarian Neoplasms,
pubmed-meshheading:16398612-Receptor, Epidermal Growth Factor,
pubmed-meshheading:16398612-Transfection
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pubmed:year |
2005
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pubmed:articleTitle |
Isolation of scFvs to in vitro produced extracellular domains of EGFR family members.
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pubmed:affiliation |
Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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