Anti-proliferative effects of mesenchymal stem cells (MSCs) derived from multiple sources on ovarian cancer cell

C Khalil1,2, M Moussa1, A Azar2

  • 1Regenerative Medicine and Inflammation Laboratory, Faculty of Medicine, Saint-Joseph University, Beirut, Lebanon.

Insights

Mesenchymal stem cells (MSCs) inhibit ovarian cancer aggressiveness by increasing apoptosis and reducing tumor markers. MSCs and their conditioned media show potential as therapeutic tools for ovarian cancer treatment.

Area of Science:

  • Stem cell biology
  • Oncology
  • Immunology

Background:

  • Mesenchymal stem cells (MSCs) are promising for disease treatment, but their impact on cancer requires further investigation.
  • The therapeutic potential of MSCs against ovarian cancer remains incompletely understood.

Purpose of the Study:

  • To investigate the effects of human bone marrow (BM), adipose tissue (AT), and umbilical cord-derived MSCs (UC-MSCs) on ovarian cancer cells.
  • To evaluate the anti-cancer properties of MSCs and their conditioned media (CM-MSC).

Main Methods:

  • Co-culture of ovarian cancer cell lines (OVCAR3, CAOV3, IGROV3, SKOV3) with MSCs and CM-MSC.
  • Analysis of tumor markers (CA-125, LDH, beta-hCG) using ELISA.
  • Flow cytometry (FCM) for proliferation and apoptosis.
  • RT-PCR for MMPs, TIMPs, and cytokine expression.

Main Results:

  • MSCs and CM-MSC significantly increased cancer cell apoptosis and reduced tumor markers (CA-125, LDH, beta-hCG).
  • Reduced cancer cell tumorigenicity (CD24 expression), invasion, and aggressiveness were observed.
  • Decreased expression of MMP-2, MMP-9, and CA-125 mRNA, with increased TIMP 1, 2, and 3 mRNA expression.
  • Modulation of cytokine profiles, including increased IL-4 and IL-10, and decreased GM-CSF, IL-6, and IL-9.

Conclusions:

  • MSCs from various sources and their conditioned media exhibit significant anti-cancer effects on ovarian cancer.
  • These findings suggest MSCs hold considerable potential as a therapeutic strategy for ovarian cancer.

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