Engineered mesenchymal stem cell-derived exosomes with high CXCR4 levels for targeted siRNA gene therapy against cancer.

Abstract

Gene therapy has been used in a variety of diseases and shows brilliant anticancer or cancer suppression effects. Gene therapy is gradually evolving as the most compelling frontier hotspot in the field of cancer therapy. The current vehicles used in gene therapy have poor safety and low delivery efficiency, and thus, it is urgent to develop novel delivery vehicles for gene therapy. Due to the excellent stability and biosafety of exosomes, their use as drug carriers for novel nucleic acid therapy is in full swing, revealing huge prospects for clinical application. Mesenchymal stem cells (MSCs) have a natural homing property and can spontaneously accumulate at injury sites, inflammation sites, and even tumour sites. This feature is attributed to a variety of tropism factors expressed on their surface; for example, CXC chemokine receptor type 4 (CXCR4) can specifically bind to the highly expressed stromal cell derived factor-1 (SDF-1) on the tumour surface, which is essential for accumulation of MSCs at the tumour site. The mesenchymal stem cells used in this study were genetically engineered to obtain exosomes with high CXCR4 expression as carriers for targeted gene-drug delivery, and then, the Survivin gene was loaded via electrotransformation to construct a brand-new gene-drug delivery system (CXCR4high Exo/si-Survivin). Finally, related in vivo and in vitro experiments were conducted. We observed that the new delivery system can efficiently aggregate at the tumour site and release siRNA into tumour cells, knocking down the Survivin gene in tumour cells in vivo and thereby inhibiting tumour growth. This new gene-drug delivery system has tremendous clinical transformation value and provides a new strategy for clinical treatment of tumours.

• Authors: Shuyue Xu, Bin Liu, Junyi Fan, Cuili Xue, Yi Lu, Can Li, Daxiang Cui
• Journal: Nanoscale (Nanoscale) Vol. 14 Issue 11 Pg. 4098-4113 (Mar 17 2022) ISSN: 2040-3372 [Electronic] England
• PMID: 35133380 (Publication Type: Journal Article)

Chemical References

• CXCR4 protein, human
• Chemokine CXCL12
• RNA, Small Interfering
• Receptors, CXCR4

Topics

• Chemokine CXCL12 (genetics)
• Exosomes (metabolism)
• Genetic Therapy
• Humans
• Mesenchymal Stem Cells
• Neoplasms (metabolism, therapy)
• RNA, Small Interfering (metabolism)
• Receptors, CXCR4 (genetics)