Mesenchymal stem cells expressing interleukin-18 suppress breast cancer cells in vitro

Xiaoyi Liu1, Jianxia Hu2, Suyuan Sun3

  • 1Department of Galactophore, The Second Hospital of Shandong University, Jinan, Shandong 250033, P.R. China ; Department of Galactophore, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China.

Insights

Genetically modified human mesenchymal stem cells (hUMSCs) expressing interleukin 18 (IL-18) suppressed breast cancer cell growth, migration, and invasion. This novel gene therapy approach shows promise for treating breast cancer.

Area of Science:

  • Oncology
  • Gene Therapy
  • Stem Cell Biology

Background:

  • Breast cancer is a leading global malignancy with treatment challenges due to disease heterogeneity.
  • Current therapies often yield unsatisfactory outcomes, highlighting the need for innovative treatment strategies.
  • Cancer gene therapy aims to develop more effective treatments for various cancers, including breast cancer.

Purpose of the Study:

  • To investigate the efficacy of human mesenchymal stem cells derived from umbilical cord (hUMSCs) genetically modified with the interleukin 18 (IL-18) gene.
  • To evaluate the effects of hUMSCs/IL-18 on the proliferation, migration, and invasion of MCF-7 and HCC1937 breast cancer cells in vitro.
  • To explore the potential of hUMSCs/IL-18 as a novel antitumor therapy for breast cancer.

Main Methods:

  • Lentiviral systems were used for efficient genetic modification of hUMSCs to stably express IL-18.
  • In vitro experiments were conducted using MCF-7 and HCC1937 breast cancer cell lines.
  • Assays were performed to assess cell proliferation, migration, and invasion following treatment with hUMSCs/IL-18.

Main Results:

  • Transduced hUMSCs stably expressed IL-18 protein.
  • hUMSCs/IL-18 significantly suppressed the proliferation, migration, and invasion of both MCF-7 and HCC1937 cells.
  • The suppression of proliferation appeared to involve the induction of G1- to S-phase arrest in breast cancer cells.

Conclusions:

  • hUMSCs genetically modified with IL-18 demonstrate significant antitumor effects against breast cancer cells in vitro.
  • The hUMSCs/IL-18 therapy effectively inhibits cancer cell growth, migration, and invasion.
  • This approach offers a potential new avenue for developing effective gene therapies for breast cancer treatment.