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[Retracted] Upregulation of GRIM‑19 inhibits the growth and invasion of human breast cancer cells
- Source :
- Molecular Medicine Reports. 24
- Publication Year :
- 2021
- Publisher :
- Spandidos Publications, 2021.
-
Abstract
- Gene associated with retinoid-interferon (IFN)-induced mortality 19 (GRIM-19), a novel IFN-β/retinoic acid-inducible gene product, has been identified as a potential tumor suppressor, which is associated with the inhibition of tumor growth. GRIM-19 has been demonstrated to be downregulated in the ovarian tissue of patients with breast cancer, however, its role in breast cancer remains to be fully elucidated. In the present study, a recombinant eukaryotic expression plasmid carrying GRIM-19 was constructed and then transfected into the MCF7 human breast cancer cell line to examine its effects on breast cancer cell growth, migration and invasion using several in vitro approaches. The results demonstrated that upregulation GRIM-19 in the MCF7 cells significantly inhibited cell proliferation, colony formation, migration and invasion, and induced cell apoptosis. Additionally, upregulation of GRIM-19 also suppressed the secretion of urokinase-type plasminogen activator (u-PA), matrix metalloproteinase (MMP)-2, MMP-9 and vascular endothelial growth factor (VEGF). It was also demonstrated that the activation of signal transducer and activator of transcription 3 (STAT3) was downregulated by the expression of GRIM-19. These results revealed that overexpression of the GRIM-19 gene may be an effective approach to control the growth and invasion of human breast cancer cells.
- Subjects :
- Cancer Research
animal structures
Oncogene
Cell growth
fungi
Cancer
Biology
Cell cycle
medicine.disease
Biochemistry
Vascular endothelial growth factor
chemistry.chemical_compound
Breast cancer
Oncology
chemistry
Cancer cell
Genetics
Cancer research
medicine
biology.protein
Molecular Medicine
STAT3
Molecular Biology
Subjects
Details
- ISSN :
- 17913004 and 17912997
- Volume :
- 24
- Database :
- OpenAIRE
- Journal :
- Molecular Medicine Reports
- Accession number :
- edsair.doi...........b169ee106febf6df4422aadfc429f251