Pleiotrophin
(PTN) is a secreted cytokine that is expressed in various cancer cell
lines and human tumor such as colon cancer, lung cancer, gastric cancer
and melanoma. It plays significant roles in angiogenesis, metastasis,
differentiation and cell growth. The expression of PTN in the adult is
limited to the hippocampus in an activity-dependent manner, making it a
very attractive target for cancer therapy. RNA interference (RNAi)
offers great potential as a new powerful therapeutic strategy based on
its highly specific and efficient silencing of a target gene. However,
efficient delivery of small interfering RNA (siRNA) in vivo remains a
significant hurdle for its successful therapeutic application. In this
study, we first identified, on a cell-based experiment, applying a 1:1
mixture of two PTN specific siRNA engenders a higher silencing
efficiency on both mRNA and protein level than using any of them
discretely at the same dose. As a consequence, slower melanoma cells
growth was also observed for using two specific siRNA combinatorially.
To establish a robust way for siRNA delivery in vivo and further
investigate how silence of PTN affects tumor growth, we tested three
different methods to deliver siRNA in vivo: first non-targeted in-vivo
delivery of siRNA via jetPEI; second lung targeted delivery of siRNA via
microbubble coated jetPEI; third tumor cell targeted delivery of siRNA
via transferrin-polyethylenimine (Tf-PEI). As a result, we found that
all three in-vivo siRNAs delivery methods led to an evident inhibition
of melanoma growth in non-immune deficiency C57BL/6 mice without a
measureable change of ALT and AST activities. Both targeted delivery
methods showed more significant curative effect than jetPEI. The lung
targeted delivery by microbubble coated jetPEI revealed a comparable
therapeutic effect with Tf-PEI, indicating its potential application for
target delivery of siRNA in vivo.
- PMID:
- 28562667
- PMCID:
- PMC5451024
- DOI:
- 10.1371/journal.pone.0177964
- [Indexed for MEDLINE]
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