AI Article Synopsis

  • Despite advancements in glioma treatment, patient prognosis remains poor, highlighting the need for innovative therapies.
  • Umbilical cord-derived mesenchymal stromal/stem cells (UC-MSCs) show potential as effective carriers for delivering interleukin 24 (IL-24), which can target and kill tumor cells without harming normal cells.
  • Research demonstrates that UC-MSCs can migrate to glioma cells and that IL-24-UC-MSC injections significantly reduce tumor growth in glioma models, suggesting a promising avenue for future glioma therapies.

Article Abstract

Although much progress has been made in the treatment of gliomas, the prognosis for patients with gliomas is still very poor. Stem cell-based therapies may be promising options for glioma treatment. Recently, many studies have reported that umbilical cord-derived mesenchymal stromal/stem cells (UC-MSCs) are ideal gene vehicles for tumor gene therapy. Interleukin 24 (IL-24) is a pleiotropic immunoregulatory cytokine that has an apoptotic effect on many kinds of tumor cells and can inhibit the growth of tumors specifically without damaging normal cells. In this study, we investigated UC-MSCs as a vehicle for the targeted delivery of IL-24 to tumor sites. UC-MSCs were transduced with lentiviral vectors carrying green fluorescent protein (GFP) or IL-24 complementary DNA. The results indicated that UC-MSCs could selectively migrate to glioma cells in vitro and in vivo. Injection of IL-24-UC-MSCs significantly suppressed tumor growth of glioma xenografts. The restrictive efficacy of IL-24-UC-MSCs was associated with the inhibition of proliferation as well as the induction of apoptosis in tumor cells. These findings indicate that UC-MSC-based IL-24 gene therapy may be able to suppress the growth of glioma xenografts, thereby suggesting possible future therapeutic use in the treatment of gliomas.

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http://dx.doi.org/10.1002/jcp.29095DOI Listing

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