Leukocytes and drug-resistant cancer cells are targets for intracellular delivery by adenoviral dodecahedron

被引:5
作者
Jedynak, Marta [1 ]
Laurin, David [2 ,3 ]
Dolega, Patryk [1 ]
Podsiadla-Bialoskorska, Malgorzata [1 ]
Szurgot, Inga [1 ,5 ]
Chroboczek, Jadwiga [1 ,4 ]
Szolajska, Ewa [1 ]
机构
[1] Polish Acad Sci, Inst Biochem & Biophys, Warsaw, Poland
[2] Univ Grenoble Alpes, Etab Francais Sang, IAB, Inserm U1209, Grenoble, France
[3] CNRS UMR5309, Grenoble, France
[4] Univ Grenoble Alpes, Grenoble GNP, CNRS, TIMC IMAG, Grenoble, France
[5] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Stockholm, Sweden
关键词
Adenoviral dodecahedron; Virus like particle; Drug delivery; drug resistance; in vivo imaging; SENSITIVE POLYMERIC MICELLES; ALPHA-V INTEGRINS; HEPARAN-SULFATE; GENE DELIVERY; PHASE-III; MES-SA; VIRUS; DOXORUBICIN; NANOPARTICLES; ATTACHMENT;
D O I
10.1016/j.nano.2018.05.001
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
One of the major factors limiting the effectiveness of cancer chemotherapy is inefficient drug delivery. Systems enabling efficient delivery and enhanced intracellular uptake appear particularly promising in this respect. Virus-like particle, adenoviral dodecahedron (Dd), employs receptor-mediated endocytosis for cell penetration and is able to deliver intracellularly dozens of cargo molecules attached to one particle. We focused on studying Dd properties in the context of cancer treatment, showing that intratumoral injection of Dd, assessed in mouse xenograft model, results in vector accumulation in tumor without spreading in off-target organs. Moreover, we demonstrated that Dd is a promising vector targeting leukocytes and drug-resistant cancer cells. Dd uptake by human blood cells analyzed in vitro indicated the preference for leukocytes in comparison to red blood cells and platelets. Furthermore, internalization of Dd-doxorubicin conjugate by drugresistant cells leads to increased nuclear accumulation of doxorubicin and significant enhancement of cytotoxicity against target cancer cells. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:1853 / 1865
页数:13
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