Tissue-Penetrating Delivery of Compounds and Nanoparticles into Tumors

被引:960
作者
Sugahara, Kazuki N. [1 ]
Teesalu, Tambet [1 ]
Karmali, Priya Prakash [2 ]
Kotamraju, Venkata Ramana [1 ]
Agemy, Lilach [1 ]
Girard, Olivier M. [3 ]
Hanahan, Douglas [4 ,5 ]
Mattrey, Robert F. [3 ]
Ruoslahti, Erkki [1 ,2 ]
机构
[1] Univ Calif Santa Barbara, Burnham Inst Med Res, Vasc Mapping Ctr, Santa Barbara, CA 93106 USA
[2] Burnham Inst Med Res, Canc Res Ctr, La Jolla, CA 92037 USA
[3] Univ Calif San Diego, Dept Radiol, San Diego, CA 92103 USA
[4] Univ Calif San Francisco, Dept Biochem & Biophys, Ctr Diabet, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Biochem & Biophys, Ctr Comprehens Canc, San Francisco, CA 94143 USA
关键词
ENDOTHELIAL GROWTH-FACTOR; IN-VIVO; DRUG-DELIVERY; MOUSE MODEL; CANCER-TREATMENT; PROSTATE-CANCER; TRANSGENIC MICE; PHAGE DISPLAY; CD44; CLEAVAGE; CELL;
D O I
10.1016/j.ccr.2009.10.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Poor penetration of drugs into tumors is a major obstacle in tumor treatment. We describe a strategy for peptide-mediated delivery of compounds deep into the tumor parenchyma that uses a tumor-homing peptide, iRGD (CRGDK/RGPD/EC). Intravenously injected compounds coupled to iRGD bound to tumor vessels and spread into the extravascular tumor parenchyma, whereas conventional RGD peptides; only delivered the cargo to the blood vessels. iRGD homes to tumors through a three-step process: the RGD motif mediates binding to alpha v integrins on tumor endothelium and a proteolytic cleavage then exposes a binding motif for neuropilin-1, which mediates penetration into tissue and cells. Conjugation to iRGD significantly improved the sensitivity of tumor-imaging agents and enhanced the activity of an antitumor drug.
引用
收藏
页码:510 / 520
页数:11
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