Cargando…

Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer

Delivery of nucleic acids into solid tumor environments remains a pressing challenge. This study examines the ability of macrophages to horizontally transfer small interfering RNA (siRNA) lipoplexes to cancer cells. Macrophages are a natural candidate for a drug carrier because of their ability to a...

Descripción completa

Detalles Bibliográficos
Autores principales: Wayne, Elizabeth C., Long, Christian, Haney, Matthew J., Batrakova, Elena V., Leisner, Tina M., Parise, Leslie V., Kabanov, Alexander V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839649/
https://www.ncbi.nlm.nih.gov/pubmed/31728272
http://dx.doi.org/10.1002/advs.201900582
_version_ 1783467471544516608
author Wayne, Elizabeth C.
Long, Christian
Haney, Matthew J.
Batrakova, Elena V.
Leisner, Tina M.
Parise, Leslie V.
Kabanov, Alexander V.
author_facet Wayne, Elizabeth C.
Long, Christian
Haney, Matthew J.
Batrakova, Elena V.
Leisner, Tina M.
Parise, Leslie V.
Kabanov, Alexander V.
author_sort Wayne, Elizabeth C.
collection PubMed
description Delivery of nucleic acids into solid tumor environments remains a pressing challenge. This study examines the ability of macrophages to horizontally transfer small interfering RNA (siRNA) lipoplexes to cancer cells. Macrophages are a natural candidate for a drug carrier because of their ability to accumulate at high densities into many cancer types, including, breast, prostate, brain, and colon cancer. Here, it is demonstrated that macrophages can horizontally transfer siRNA to cancer cells during in vitro coculture. The amount of transfer can be dosed depending on the amount of siRNA loaded and total number of macrophages delivered. Macrophages loaded with calcium integrin binding protein‐1 (CIB1)‐siRNA result in decreased tumorsphere growth and decreased mRNA expression of CIB1 and KI67 in MDA‐MB‐468 human breast cancer cells. Adoptive transfer of macrophages transfected with CIB1‐siRNA localizes to the orthotopic MDA‐MB‐468 tumor. Furthermore, it is reported that macrophage activation can modulate this transfer process as well as intracellular trafficking protein Rab27a. As macrophages are heavily involved in tumor progression, understanding how to use macrophages for drug delivery can substantially benefit the treatment of tumors.
format Online
Article
Text
id pubmed-6839649
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-68396492019-11-14 Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer Wayne, Elizabeth C. Long, Christian Haney, Matthew J. Batrakova, Elena V. Leisner, Tina M. Parise, Leslie V. Kabanov, Alexander V. Adv Sci (Weinh) Full Papers Delivery of nucleic acids into solid tumor environments remains a pressing challenge. This study examines the ability of macrophages to horizontally transfer small interfering RNA (siRNA) lipoplexes to cancer cells. Macrophages are a natural candidate for a drug carrier because of their ability to accumulate at high densities into many cancer types, including, breast, prostate, brain, and colon cancer. Here, it is demonstrated that macrophages can horizontally transfer siRNA to cancer cells during in vitro coculture. The amount of transfer can be dosed depending on the amount of siRNA loaded and total number of macrophages delivered. Macrophages loaded with calcium integrin binding protein‐1 (CIB1)‐siRNA result in decreased tumorsphere growth and decreased mRNA expression of CIB1 and KI67 in MDA‐MB‐468 human breast cancer cells. Adoptive transfer of macrophages transfected with CIB1‐siRNA localizes to the orthotopic MDA‐MB‐468 tumor. Furthermore, it is reported that macrophage activation can modulate this transfer process as well as intracellular trafficking protein Rab27a. As macrophages are heavily involved in tumor progression, understanding how to use macrophages for drug delivery can substantially benefit the treatment of tumors. John Wiley and Sons Inc. 2019-09-04 /pmc/articles/PMC6839649/ /pubmed/31728272 http://dx.doi.org/10.1002/advs.201900582 Text en © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Wayne, Elizabeth C.
Long, Christian
Haney, Matthew J.
Batrakova, Elena V.
Leisner, Tina M.
Parise, Leslie V.
Kabanov, Alexander V.
Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer
title Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer
title_full Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer
title_fullStr Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer
title_full_unstemmed Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer
title_short Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer
title_sort targeted delivery of sirna lipoplexes to cancer cells using macrophage transient horizontal gene transfer
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839649/
https://www.ncbi.nlm.nih.gov/pubmed/31728272
http://dx.doi.org/10.1002/advs.201900582
work_keys_str_mv AT wayneelizabethc targeteddeliveryofsirnalipoplexestocancercellsusingmacrophagetransienthorizontalgenetransfer
AT longchristian targeteddeliveryofsirnalipoplexestocancercellsusingmacrophagetransienthorizontalgenetransfer
AT haneymatthewj targeteddeliveryofsirnalipoplexestocancercellsusingmacrophagetransienthorizontalgenetransfer
AT batrakovaelenav targeteddeliveryofsirnalipoplexestocancercellsusingmacrophagetransienthorizontalgenetransfer
AT leisnertinam targeteddeliveryofsirnalipoplexestocancercellsusingmacrophagetransienthorizontalgenetransfer
AT pariselesliev targeteddeliveryofsirnalipoplexestocancercellsusingmacrophagetransienthorizontalgenetransfer
AT kabanovalexanderv targeteddeliveryofsirnalipoplexestocancercellsusingmacrophagetransienthorizontalgenetransfer