Conditional internalization of PEGylated nanomedicines by PEG engagers for triple negative breast cancer therapy

被引:70
作者
Su, Yu-Cheng [1 ]
Burnouf, Pierre-Alain [1 ,2 ,3 ]
Chuang, Kuo-Hsiang [4 ]
Chen, Bing-Mae [1 ]
Cheng, Tian-Lu [5 ]
Roffler, Steve R. [1 ,6 ]
机构
[1] Acad Sinica, Inst Biomed Sci, Taipei 11529, Taiwan
[2] Natl Yang Ming Univ, Taiwan Int Grad Program Mol Med, Taipei 11529, Taiwan
[3] Acad Sinica, Taipei 11529, Taiwan
[4] Taipei Med Univ, Grad Inst Pharmacognosy, Taipei 11031, Taiwan
[5] Kaohsiung Med Univ, Dept Biomed Sci & Environm Biol, Ctr Biomarkers & Biotech Drugs, Kaohsiung 80708, Taiwan
[6] Kaohsiung Med Univ, Grad Inst Med, Kaohsiung 80708, Taiwan
关键词
GROWTH-FACTOR RECEPTOR; LIPOSOMAL DOXORUBICIN; POLYETHYLENE-GLYCOL; PHASE-II; MONOCLONAL-ANTIBODY; EFFICACY; EGFR; HETEROGENEITY; NANOPARTICLES; COMBINATION;
D O I
10.1038/ncomms15507
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Triple-negative breast cancer (TNBC) lacks effective treatment options due to the absence of traditional therapeutic targets. The epidermal growth factor receptor (EGFR) has emerged as a promising target for TNBC therapy because it is overexpressed in about 50% of TNBC patients. Here we describe a PEG engager that simultaneously binds polyethylene glycol and EGFR to deliver PEGylated nanomedicines to EGFR(+) TNBC. The PEG engager displays conditional internalization by remaining on the surface of TNBC cells until contact with PEGylated nanocarriers triggers rapid engulfment of nanocargos. PEG engager enhances the anti-proliferative activity of PEG-liposomal doxorubicin to EGFR(+) TNBC cells by up to 100-fold with potency dependent on EGFR expression levels. The PEG engager significantly increases retention of fluorescent PEG probes and enhances the antitumour activity of PEGylated liposomal doxorubicin in human TNBC xenografts. PEG engagers with specificity for EGFR are promising for improved treatment of EGFR(+) TNBC patients.
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页数:12
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