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

AI Article Synopsis

  • This study explores using macrophages as a delivery system for siRNA to target cancer cells in solid tumors, an area that presents significant challenges in treatment.
  • It was found that macrophages can effectively transfer siRNA to cancer cells, with the efficiency depending on the amount of siRNA and the number of macrophages used.
  • Specifically, using CIB1-siRNA within macrophages reduced tumor growth and gene expression in breast cancer cells, indicating that manipulating macrophages could enhance cancer treatment strategies.

Article Abstract

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 . As macrophages are heavily involved in tumor progression, understanding how to use macrophages for drug delivery can substantially benefit the treatment of tumors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839649PMC
http://dx.doi.org/10.1002/advs.201900582DOI Listing

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