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Applied Biochemistry and Biotechnology

, Volume 187, Issue 1, pp 352–364 | Cite as

Engineered Exosomes for Targeted Transfer of siRNA to HER2 Positive Breast Cancer Cells

  • Shabanali Khodashenas Limoni
  • Mehdi Forouzandeh MoghadamEmail author
  • Seyed Mohammad Moazzeni
  • Hosna Gomari
  • Fatemeh Salimi
Article

Abstract

Exosomes are the best options for gene targeting, because of their natural, nontoxic, non-immunogenic, biodegradable, and targetable properties. By engineering exosome-producing cells, ligands can be expressed fusing with exosomal surface proteins for targeting cancer cell receptors. In the present study, HER2-positive breast cancer cells were targeted with a modified exosome producing engineered HEK293T cell. For this purpose, the HEK293T cells were transduced by a lentiviral vector bearing-LAMP2b-DARPin G3 chimeric gene. Stable cells expressing the fusion protein were selected, and the exosomes produced by these cells were isolated from the culture medium, characterized, and then loaded with siRNA for subsequent delivery to the SKBR3 cells. Our results showed that stable HEK293T cells produced DARPin G3 on the surface of exosomes. These exosomes can bind specifically to HER2/Neu and are capable of delivering siRNA molecules against TPD52 gene into SKBR3 cell line down-regulating the gene expression up to 70%. Present approach is envisaged to facilitate genes and drugs transfer to HER2 cancer cells providing additional option for gene therapy and drug delivery.

Keywords

Exosome HER2 siRNA delivery TPD52 Lentiviral vector 

Notes

Funding Information

This work was supported by educational program grant from Tarbiat Modares University and Iranian national science foundation: INSF (code No: 90006884).

Compliance with Ethical Standards

Conflict of Interest

The authors declare that they have no conflict of interest.

Supplementary material

12010_2018_2813_MOESM1_ESM.doc (36 kb)
ESM 1 (DOC 35 kb)

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of Medical Biotechnology, Faculty of Medical ScienceTarbiat Modares UniversityTehranIran
  2. 2.Immunogenetic Research CenterMazandaran University of Medical SciencesSariIran
  3. 3.Department of Medical Immunology, Faculty of Medical ScienceTarbiat Modares UniversityTehranIran

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