Coadministration of a Tumor-Penetrating Peptide Enhances the Efficacy of Cancer Drugs

Author:

Sugahara Kazuki N.1,Teesalu Tambet1,Karmali Priya Prakash2,Kotamraju Venkata Ramana1,Agemy Lilach1,Greenwald Daniel R.3,Ruoslahti Erkki12

Affiliation:

1. Vascular Mapping Laboratory, Center for Nanomedicine, Sanford-Burnham Medical Research Institute at University of California at Santa Barbara, Biology II Building, University of California, Santa Barbara, CA 93106–9610, USA.

2. Cancer Research Center, Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.

3. Santa Barbara Hematology Oncology Medical Group, Cancer Center of Santa Barbara, 540 West Pueblo Street, Santa Barbara, CA 93105, USA.

Abstract

Penetrating Attack on Tumors While considerable research effort in oncology is focused on the design of new cancer drugs, an important but relatively understudied research area is the development of methods that optimize the delivery and tumor penetration of existing cancer drugs. Previous work has characterized a peptide (iRGD) that selectively targets and penetrates tumor tissue by virtue of its specific interaction with tumor blood vessels. Now, studying mouse models, Sugahara et al. (p. 1031 , see the cover) show that coinjection of the iRGD peptide increases the tumor penetration and antitumor activity of several cancer drugs, including the cytotoxic agent doxorubicin and the therapeutic antibody trastuzumab (Herceptin), without increasing their harmful effects on healthy tissue. Importantly, these effects did not require chemical conjugation of the cancer drugs to the peptide.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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