Engineering mesenchymal stem cells: a novel therapeutic approach in breast cancer

被引:17
|
作者
Heidari, Razieh [1 ]
Dehkordi, Neda Gholamian [2 ]
Mohseni, Roohollah [3 ]
Safaei, Mohsen [1 ]
机构
[1] Shahrekord Univ Med Sci, Sch Adv Technol, Dept Med Biotechnol, Shahrekord, Iran
[2] Shahrekord Univ Med Sci, Sch Adv Technol, Dept Mol Med, Shahrekord, Iran
[3] Shahrekord Univ Med Sci, Clin Biochem Res Ctr, Basic Hlth Sci Inst, Shahrekord, Iran
关键词
Mesenchymal stem cells; breast cancer; tumour homing; targeted drug delivery vehicle; genetic modification; DRUG-DELIVERY; STROMAL CELLS; TUMOR-GROWTH; IN-VITRO; TARGETED DELIVERY; GENE-THERAPY; MIGRATION; INHIBIT; LUNG; VIVO;
D O I
10.1080/1061186X.2020.1775842
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Breast cancer is one of the most prevalent and deadliest cancers among women in the world because of its aggressive behaviour and inadequate response to conventional therapies. Cellular and gene therapies based on mesenchymal stem cells (MSCs) represent promising treatment strategies for multiple diseases, such as cancers. MSCs are multipotent adult stem cells with important features for cell therapy, such as tissue homing to injured sites, their differentiation potential, their capacity of secreting plenty of trophic factors, and low immunogenicity. The quite easy isolation of these cells from various types of tissues are associated with no ethical concern when dealing with foetal or embryonic stem cells. The MSCs exhibit both pro and anti-oncogenic properties. However, genetic engineering of MSCs and nanoparticles is being employed as a means to solve some of these problems and improve the antitumor properties of these cells. The tumour-homing ability of MSCs and their exosomes to tumour niches have made them as a promising vector for targeted delivery of therapeutic agents to tumours site. The present study investigated MSCs specifications, pro- and anti-oncogenic properties of MSCs in breast cancer, and reviewed targeted breast cancer therapyviaengineered MSCs, likely as potent cellular vehicles.
引用
收藏
页码:732 / 741
页数:10
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