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Published on: January 18, 2017
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.
Abstract:
Breast cancer is the most common malignancy among females throughout the world. Current treatments have unsatisfactory outcomes due to the dispersed nature of certain types of the disease. The development of a more effective therapy for breast cancer has long been one of the most elusive goals of cancer gene therapy. In the present study, human mesenchymal stem cells derived from umbilical cord (hUMSCs) genetically modified with interleukin 18 (IL-18) gene were used to study the effect of hUMSCs/IL-18 on the growth, migration and invasion of MCF-7 and HCC1937 cells in vitro. The hUMSCs could be efficiently modified by lentiviral systems and stably expressed IL-18 protein. hUMSCs/IL-18, but not hUMSCs without the IL-18 gene transduction, significantly suppressed the proliferation, migration and invasion of the MCF-7 and HCC1937 cells. The mechanism of this proliferation suppression may have involved the induction of G1- to S-phase arrest of the breast cancer cells by the hUMSCs/IL-18. In conclusion, hUMSCs/IL-18 can suppress the proliferation, migration and invasion of breast cancer cells in vitro and may provide an approach for a novel antitumor therapy in breast cancer.
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.
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