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肽类肿瘤靶向制剂:从噬菌体展示肽筛选到临床应用。

Peptidic tumor targeting agents: the road from phage display peptide selections to clinical applications.

机构信息

Division of Translational Medicine Departments of Internal Medicine and The Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9185, USA.

出版信息

Curr Pharm Des. 2010;16(9):1040-54. doi: 10.2174/138161210790963788.


DOI:10.2174/138161210790963788
PMID:20030617
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4126568/
Abstract

Cancer has become the number one cause of death amongst Americans, killing approximately 1,600 people per day. Novel methods for early detection and the development of effective treatments are an eminent priority in medicine. For this reason, isolation of tumor-specific ligands is a growing area of research. Tumor-specific binding agents can be used to probe the tumor cell surface phenotype and to customize treatment accordingly by conjugating the appropriate cell-targeting ligand to an anticancer drug. This refines the molecular diagnosis of the tumor and creates guided drugs that can target the tumor while sparing healthy tissues. Additionally, these targeting agents can be used as in vivo imaging agents that allow for earlier detection of tumors and micrometastasis. Phage display is a powerful technique for the isolation of peptides that bind to a particular target with high affinity and specificity. The biopanning of intact cancer cells or tumors in animals can be used as the bait to isolate peptides that bind to cancer-specific cell surface biomarkers. Over the past 10 years, unbiased biopanning of phage-displayed peptide libraries has generated a suite of cancer targeting peptidic ligands. This review discusses the recent advances in the isolation of cancer-targeting peptides by unbiased biopanning methods and highlights the use of the isolated peptides in clinical applications.

摘要

癌症已成为美国人的头号死因,每天约有 1600 人因此死亡。在医学领域,寻找新的早期检测方法和开发有效的治疗方法是当务之急。出于这个原因,肿瘤特异性配体的分离已成为一个研究热点。肿瘤特异性结合剂可用于探测肿瘤细胞表面表型,并通过将适当的细胞靶向配体与抗癌药物连接,从而有针对性地进行治疗。这可以改进肿瘤的分子诊断,并生成导向药物,既能靶向肿瘤,又能保护健康组织。此外,这些靶向药物可用作体内成像剂,以便更早地检测肿瘤和微转移。噬菌体展示是一种强大的技术,可以分离出与特定目标具有高亲和力和特异性的肽。可以使用完整的癌细胞或动物肿瘤作为诱饵,来分离与癌症特异性细胞表面生物标志物结合的肽。在过去的 10 年中,通过无偏性噬菌体展示肽文库的生物淘选,已经产生了一系列针对癌症的靶向肽配体。本文讨论了通过无偏性生物淘选方法分离癌症靶向肽的最新进展,并强调了所分离的肽在临床应用中的用途。

相似文献

[1]
Peptidic tumor targeting agents: the road from phage display peptide selections to clinical applications.

Curr Pharm Des. 2010

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
Cancer-specific ligands identified from screening of peptide-display libraries.

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[9]
Biopanning of phage displayed peptide libraries for the isolation of cell-specific ligands.

Methods Mol Biol. 2009

[10]
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J Transl Med. 2012-9-19

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[8]
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[10]
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本文引用的文献

[1]
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J Mater Chem. 2009

[2]
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Phase Ib study of NGR-hTNF, a selective vascular targeting agent, administered at low doses in combination with doxorubicin to patients with advanced solid tumours.

Br J Cancer. 2009-7-21

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J Clin Oncol. 2009-7-20

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Identification of a novel dual E- and N-cadherin antagonist.

Peptides. 2009-8

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Screening and identification of a peptide specifically targeted to NCI-H1299 from a phage display peptide library.

Cancer Lett. 2009-8-18

[8]
Antiangiogenic targeting liposomes increase therapeutic efficacy for solid tumors.

J Biol Chem. 2009-5-8

[9]
Romiplostim.

Drugs. 2009

[10]
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Front Biosci (Landmark Ed). 2009-1-1

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