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Fluorescent-Antibody Targeting of Insulin-Like Growth Factor-1 Receptor Visualizes Metastatic Human Colon Cancer in Orthotopic Mouse Models
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 박정엽 | - |
| dc.date.accessioned | 2017-02-24T03:08:30Z | - |
| dc.date.available | 2017-02-24T03:08:30Z | - |
| dc.date.issued | 2016 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/146255 | - |
| dc.description.abstract | Fluorescent-antibody targeting of metastatic cancer has been demonstrated by our laboratory to enable tumor visualization and effective fluorescence-guided surgery. The goal of the present study was to determine whether insulin-like growth factor-1 receptor (IGF-1R) antibodies, conjugated with bright fluorophores, could enable visualization of metastatic colon cancer in orthotopic nude mouse models. IGF-1R antibody (clone 24-31) was conjugated with 550 nm, 650 nm or PEGylated 650 nm fluorophores. Subcutaneous, orthotopic, and liver metastasis models of colon cancer in nude mice were targeted with the fluorescent IGF-1R antibodies. Western blotting confirmed the expression of IGF-1R in HT-29 and HCT 116 human colon cancer cell lines, both expressing green fluorescent protein (GFP). Labeling with fluorophore-conjugated IGF-1R antibody demonstrated fluorescent foci on the membrane of colon cancer cells. Subcutaneously- and orthotopically-transplanted HT-29-GFP and HCT 116-GFP tumors brightly fluoresced at the longer wavelengths after intravenous administration of fluorescent IGF-1R antibodies. Orthotopically-transplanted HCT 116-GFP tumors were brightly labeled by fluorescent IGF-1R antibodies such that they could be imaged non-invasively at the longer wavelengths. In an experimental liver metastasis model, IGF-1R antibodies conjugated with PEGylated 650 nm fluorophores selectively highlighted the liver metastases, which could then be non-invasively imaged. The IGF-1R fluorescent-antibody labeled liver metastases were very bright compared to the normal liver and the fluorescent-antibody label co-located with green fluorescent protein (GFP) expression of the colon cancer cells. The present study thus demonstrates that fluorophore-conjugated IGF-1R antibodies selectively visualize metastatic colon cancer and have clinical potential for improved diagnosis and fluorescence-guided surgery. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.format.extent | e0146504 | - |
| dc.language | English | - |
| dc.publisher | Public Library of Science | - |
| dc.relation.isPartOf | PLOS ONE | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
| dc.subject.MESH | Animals | - |
| dc.subject.MESH | Cell Line, Tumor | - |
| dc.subject.MESH | Colonic Neoplasms/metabolism* | - |
| dc.subject.MESH | Colonic Neoplasms/pathology | - |
| dc.subject.MESH | Disease Models, Animal | - |
| dc.subject.MESH | Fluorescent Antibody Technique | - |
| dc.subject.MESH | Green Fluorescent Proteins/metabolism | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Liver Neoplasms/metabolism* | - |
| dc.subject.MESH | Liver Neoplasms/secondary | - |
| dc.subject.MESH | Mice | - |
| dc.subject.MESH | Mice, Nude | - |
| dc.subject.MESH | Receptor, IGF Type 1/metabolism* | - |
| dc.title | Fluorescent-Antibody Targeting of Insulin-Like Growth Factor-1 Receptor Visualizes Metastatic Human Colon Cancer in Orthotopic Mouse Models | - |
| dc.type | Article | - |
| dc.publisher.location | United States | - |
| dc.contributor.college | College of Medicine | - |
| dc.contributor.department | Dept. of Internal Medicine | - |
| dc.contributor.googleauthor | Jeong Youp Park | - |
| dc.contributor.googleauthor | Takashi Murakami | - |
| dc.contributor.googleauthor | Jin Young Lee | - |
| dc.contributor.googleauthor | Yong Zhang | - |
| dc.contributor.googleauthor | Robert M. Hoffman | - |
| dc.contributor.googleauthor | Michael Bouvet | - |
| dc.identifier.doi | 10.1371/journal.pone.0146504 | - |
| dc.contributor.localId | A01647 | - |
| dc.relation.journalcode | J02540 | - |
| dc.identifier.eissn | 1932-6203 | - |
| dc.identifier.pmid | 26731105 | - |
| dc.contributor.alternativeName | Park, Jeong Youp | - |
| dc.contributor.affiliatedAuthor | Park, Jeong Youp | - |
| dc.citation.volume | 11 | - |
| dc.citation.number | 1 | - |
| dc.citation.startPage | e0146504 | - |
| dc.identifier.bibliographicCitation | PLOS ONE, Vol.11(1) : e0146504, 2016 | - |
| dc.date.modified | 2017-02-24 | - |
| dc.identifier.rimsid | 51277 | - |
| dc.type.rims | ART | - |
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