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The Effect of Human Mesenchymal Stem Cells-Conditioned Media on Glioblastoma Cells Viability In Vitro
R M Folcuti1, I Silosi1, S O Purcaru1
1PhD Student, Biochemistry Dept., Faculty of Medicine, University of Medicine and Pharmacy of Craiova.
Abstract:
A novel target for cancer treatment is based on the effects of non-tumor cells, including hMSCs on tumor growth. However, the results are controversial: some studies showed that hMSCs inhibit tumor progression, while others found they promote tumor cell proliferation. In this study, we analyse the effect of human mesenchymal cells derived from umbilical cord tissue (hUC-MSCs) and bone-marrow- mesenchymal stem cells (hBM-MSCs) on glioblastoma cells viability in vitro. GB cell cultures were established from fresh sample tissues provided by "Bagdasar-Arseni" Hospital, Bucharest, from consented GB patients. hUC-MSCs, HUC-1 and HUC-2 cell lines, were established from human umbilical cord tissue collected after delivery from natural term births at the Emergency Hospital of Craiova, Romania. hBM-MSCs cell line was purchased from Life Technologies. Conditioned media (CM) from MSCs was used to treat GB cells for 24, 48, 72 and 96 hours. To determine GB cell viability was used MTT cell proliferation assay. Statistical analyses were performed using Students t-test. hUC-MSCs CM displayed the potential to be cytotoxic to GB cells, while the treatment with hBM-MSCs CM significantly stimulated GB cell growth 24 hours after the treatment and showed minor growth cell inhibition 48, 72 and 96 hours after the treatment. This report proved that hUC-MSCsCM inhibited GB cell proliferation, while little inhibitory effect was exerted by hBM-MSCs CM.
Insights
Human umbilical cord mesenchymal stem cells (hUC-MSCs) inhibited glioblastoma cell proliferation, while bone-marrow-derived mesenchymal stem cells (hBM-MSCs) initially stimulated then slightly inhibited growth. This highlights differential effects of stem cell types on cancer progression.
Area of Science:
- Oncology
- Stem Cell Biology
- Cancer Research
Background:
- Mesenchymal stem cells (MSCs) have a controversial role in cancer, with studies showing both inhibition and promotion of tumor growth.
- Understanding the specific effects of different MSC sources, such as umbilical cord (hUC-MSCs) and bone marrow (hBM-MSCs), is crucial for targeted cancer therapies.
Purpose of the Study:
- To investigate the in vitro effects of conditioned media from human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) and bone marrow-derived mesenchymal stem cells (hBM-MSCs) on glioblastoma (GB) cell viability.
- To determine the differential impact of MSCs from distinct tissue origins on glioblastoma cell proliferation and survival.
Main Methods:
- Glioblastoma (GB) cell cultures were established from patient samples.
- Human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) and bone marrow-derived mesenchymal stem cells (hBM-MSCs) were utilized.
- GB cells were treated with conditioned media (CM) from MSCs for varying durations (24-96 hours).
- MTT cell proliferation assay was employed to assess cell viability, with statistical analysis using Student's t-test.
Main Results:
- Conditioned media from hUC-MSCs exhibited cytotoxic effects on glioblastoma cells, inhibiting their proliferation.
- Treatment with hBM-MSCs conditioned media initially stimulated GB cell growth at 24 hours.
- hBM-MSCs conditioned media showed a minor inhibitory effect on GB cell growth at later time points (48, 72, and 96 hours).
Conclusions:
- hUC-MSCs demonstrate potential as an anti-cancer agent by inhibiting glioblastoma cell proliferation.
- hBM-MSCs have a dual effect, initially promoting and later slightly inhibiting glioblastoma cell growth, indicating context-dependent roles.
- The source of mesenchymal stem cells significantly influences their therapeutic potential in glioblastoma treatment.
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