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Transcriptional Regulation of GDF15 by EGR1 Promotes Head and Neck Cancer Progression through a Positive Feedback Loop.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2021 Oct 15; Vol. 22 (20). Date of Electronic Publication: 2021 Oct 15. - Publication Year :
- 2021
-
Abstract
- Growth and differentiation factor 15 (GDF15), a divergent member of the transforming growth factor-β (TGF-β) superfamily, has been reported to be overexpressed in different kinds of cancer types. However, the function and mechanism of GDF15 in head and neck cancer (HNC) remains unclear. The Cancer Genome Atlas (TCGA) data show that the expression of GDF15 is significantly associated with tumor AJCC stage, lymph vascular invasion and tumor grade in HNC. In this study, we confirmed that knockdown of GDF15 attenuated: cell proliferation, migration and invasion via regulation of EMT through a canonical pathway; SMAD2/3 and noncanonical pathways; PI3K/AKT and MEK/ERK in HNC cell lines. Furthermore, we found that early growth response 1 (EGR1) was a transcription factor of GDF15. Interestingly, we also demonstrated that GDF15 could regulate the expression of EGR1, which meant a positive feedback loop occurred between these two factors. Moreover, combined inhibition of both GDF15 and EGR1 in a HNC mouse xenograft model showed significantly decreased tumor volume compared to inhibition of EGR1 or GDF15 alone. Our study showed that the GDF15-EGR1 signaling axis may be a good target in HNC patients.
- Subjects :
- Animals
Cell Movement genetics
Cell Proliferation genetics
Disease Progression
Early Growth Response Protein 1 physiology
Epithelial-Mesenchymal Transition genetics
Feedback, Physiological physiology
Gene Expression Regulation, Neoplastic
Growth Differentiation Factor 15 physiology
HaCaT Cells
Head and Neck Neoplasms genetics
Humans
Mice
Mice, Inbred BALB C
Mice, Nude
Signal Transduction genetics
Tumor Cells, Cultured
Early Growth Response Protein 1 genetics
Growth Differentiation Factor 15 genetics
Head and Neck Neoplasms pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 22
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 34681812
- Full Text :
- https://doi.org/10.3390/ijms222011151