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Boosting of the Enhanced Permeability and Retention Effect with Nanocapsules Improves the Therapeutic Effects of Cetuximab

Overview
Journal Cancer Biol Med
Specialty Oncology
Date 2020 Jun 27
PMID 32587779
Citations 2
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Abstract

The introduction of therapeutic antibodies (tAbs) into clinical practice has revolutionized tumor treatment strategies, but their tumor therapy efficiency is still far below expectations because of the rapid degradation and limited tumor accumulation of tAbs. : We developed a nanocapsule-based delivery system to induce the self-augmentation of the enhanced permeability and retention (EPR) effect. This system constantly penetrated across the blood-tumor barrier into the tumor while avoiding the attack of tAbs by the immune system. The biodistribution and therapeutic effect were tested with single dose administration of nanocapsule-tAbs . : The accumulation of Nano(cetuximab) within subcutaneous PC9 tumors was gradually enhanced over 6 days after single dose administration, which was contrary to the biodistribution of native cetuximab. Nano(cetuximab) accumulated in tumor tissues the EPR effect and released cetuximab. The released cetuximab acted on vascular endothelial cells to destroy the blood-tumor barrier and induce self-augmentation of the EPR effect, which in turn contributed to further tumor accumulation of long-circulating Nano(cetuximab). Compared with single dose administration of native cetuximab, Nano(cetuximab) showed an effective tumor suppressive effect for 3 weeks. : The nanocapsule-based delivery system efficiently delivered tAbs to tumor tissues and released them to boost the EPR effect, which facilitated further tumor accumulation of the tAbs. This novel self-augmentation of the EPR effect facilitated by the biological characteristics of tAbs and nanotechnology contributed to the improvement of the therapeutic effect of tAbs, and stimulated new ideas for antibody-based tumor therapy.

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References
1.
Sheng G, Bernabe K, Guo J, Warner B . Epidermal growth factor receptor-mediated proliferation of enterocytes requires p21waf1/cip1 expression. Gastroenterology. 2006; 131(1):153-64. DOI: 10.1053/j.gastro.2006.05.007. View

2.
Petrelli F, Borgonovo K, Cabiddu M, Lonati V, Barni S . Relationship between skin rash and outcome in non-small-cell lung cancer patients treated with anti-EGFR tyrosine kinase inhibitors: a literature-based meta-analysis of 24 trials. Lung Cancer. 2012; 78(1):8-15. DOI: 10.1016/j.lungcan.2012.06.009. View

3.
Li S, Schmitz K, Jeffrey P, Wiltzius J, Kussie P, Ferguson K . Structural basis for inhibition of the epidermal growth factor receptor by cetuximab. Cancer Cell. 2005; 7(4):301-11. DOI: 10.1016/j.ccr.2005.03.003. View

4.
Ciardiello F, Tortora G . EGFR antagonists in cancer treatment. N Engl J Med. 2008; 358(11):1160-74. DOI: 10.1056/NEJMra0707704. View

5.
Bustamante Alvarez J, Gonzalez-Cao M, Karachaliou N, Santarpia M, Viteri S, Teixido C . Advances in immunotherapy for treatment of lung cancer. Cancer Biol Med. 2015; 12(3):209-22. PMC: 4607819. DOI: 10.7497/j.issn.2095-3941.2015.0032. View