肽
曲妥珠单抗
紫杉醇
阿霉素
单克隆抗体
癌症研究
脂质体
癌症
血管通透性
内化
药理学
化学
医学
乳腺癌
抗体
内科学
化疗
受体
免疫学
生物化学
作者
Kazuki N. Sugahara,Tambet Teesalu,Priya Karmali,Venkata Ramana Kotamraju,Lilach Agemy,Daniel Greenwald,Erkki Ruoslahti
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2010-04-09
卷期号:328 (5981): 1031-1035
被引量:1005
标识
DOI:10.1126/science.1183057
摘要
Poor penetration of anticancer drugs into tumors can be an important factor limiting their efficacy. We studied mouse tumor models to show that a previously characterized tumor-penetrating peptide, iRGD, increased vascular and tissue permeability in a tumor-specific and neuropilin-1-dependent manner, allowing coadministered drugs to penetrate into extravascular tumor tissue. Importantly, this effect did not require the drugs to be chemically conjugated to the peptide. Systemic injection with iRGD improved the therapeutic index of drugs of various compositions, including a small molecule (doxorubicin), nanoparticles (nab-paclitaxel and doxorubicin liposomes), and a monoclonal antibody (trastuzumab). Thus, coadministration of iRGD may be a valuable way to enhance the efficacy of anticancer drugs while reducing their side effects, a primary goal of cancer therapy research.
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