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Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy.

Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy. Research Abstract Details 

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  • Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy. Abstract Text:

    xin qinXin Qin,yi wanYi Wan,meng liMeng Li,xiaochang xueXiaochang Xue,shouzhen wuShouzhen Wu,cun zhangCun Zhang,yanjie youYanjie You,weihua wangWeihua Wang,changli jiangChangli Jiang,yan liuYan Liu,wenhua zhuWenhua Zhu,yonggang ranYonggang Ran,zhen zhangZhen Zhang,wei hanWei Han,yingqi zhangYingqi Zhang,xin qinXin Qin,yi wanYi Wan,meng liMeng Li,xiaochang xueXiaochang Xue,shouzhen wuShouzhen Wu,cun zhangCun Zhang,yanjie youYanjie You,weihua wangWeihua Wang,changli jiangChangli Jiang,yan liuYan Liu,wenhua zhuWenhua Zhu,yonggang ranYonggang Ran,zhen zhangZhen Zhang,wei hanWei Han,yingqi zhangYingqi Zhang,

    Human vascular endothelia growth factor receptor 3 (VEGFR-3) is up-regulated in a variety of human cancers. It is a potentially rational target for drug delivery. To identify novel ligands with specific binding capabilities to VEGFR-3, we screened a phage display peptide library and found a consensus motif of the peptides which is displayed by the positive phages CSDxxHxWC (x is any amino acid). The phage displaying peptide CSDSWHYWC (designated as P1) exhibited the highest affinity to VEGFR-3 in phage ELISA and the chemically synthesized P1 could bind to VEGFR-3 specifically in a dose-dependent manner. In addition, the flow cytometry assay and immunofluorescence showed that the FITC labelled P1 could bind to VEGFR-3 positive carcinoma cells with specificity. Our study suggests that P1 may be a homing peptide for treatment of tumours.

    Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy. Publishing Authors By Initials

    x qinX Qin,y wanY Wan,m liM Li,x xueX Xue,s wuS Wu,c zhangC Zhang,y youY You,w wangW Wang,c jiangC Jiang,y liuY Liu,w zhuW Zhu,y ranY Ran,z zhangZ Zhang,w hanW Han,y zhangY Zhang,x qinX Qin,y wanY Wan,m liM Li,x xueX Xue,s wuS Wu,c zhangC Zhang,y youY You,w wangW Wang,c jiangC Jiang,y liuY Liu,w zhuW Zhu,y ranY Ran,z zhangZ Zhang,w hanW Han,y zhangY Zhang,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of biochemistry

    VOLUME: 142

    Page Numbers: 79-85

    Journal Abbreviation: J. Biochem.

    ISSN: 0021-924X

    DAY: 21

    MONTH: 05

    YEAR: 2007

    Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 376600

    Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy. Keywords Mesh Terms:

    KEYWORDS: Vascular Endothelial Growth Factor Recep

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy. Information

    Substance Name: Vascular Endothelial Growth Factor Recep

    Registry Number: EC 2.7.1.112

    Grant and Affiliation Information for Identification of a novel peptide ligand of human vascular endothelia growth factor receptor 3 for targeted tumour diagnosis and therapy.

    AFFILIATION: Biotechnology Center of The Fourth Military Medical University, and State Key Laboratory of Cancer Biology, 17 Chang'le West Road, 710032 Xi'an, People's Republic of China.

    Country: Japan

    Japan Research PublicationJapan Research Publication

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    MEDLINETA: J Biochem (Tokyo)

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