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Updated: Feb 18, 2026

Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
The NOTCH4-HEY1 Pathway Induces Epithelial-Mesenchymal Transition in Head and Neck Squamous Cell Carcinoma
Takahito Fukusumi1, Theresa W Guo2, Akihiro Sakai1
1Moores Cancer Center, University of California San Diego, La Jolla, California.
Abstract:
Purpose: Recently, several comprehensive genomic analyses demonstrated NOTCH1 and NOTCH3 mutations in head and neck squamous cell carcinoma (HNSCC) in approximately 20% of cases. Similar to other types of cancers, these studies also indicate that the NOTCH pathway is closely related to HNSCC progression. However, the role of NOTCH4 in HNSCC is less well understood.Experimental Design: We analyzed NOTCH4 pathway and downstream gene expression in the TCGA data set. To explore the functional role of NOTCH4, we performed in vitro proliferation, cisplatin viability, apoptosis, and cell-cycle assays. We also compared the relationships among NOTCH4, HEY1, and epithelial-mesenchymal transition (EMT)-related genes using the TCGA data set and in vitro assays.Results:HEY1 is specifically upregulated in HNSCC compared with normal tissues in the TCGA data set. NOTCH4 is more significantly related to HEY1 activation in HNSCC in comparison with other NOTCH receptors. NOTCH4 promotes cell proliferation, cisplatin resistance, inhibition of apoptosis, and cell-cycle dysregulation. Furthermore, NOTCH4 and HEY1 upregulation resulted in decreased E-cadherin expression and increased Vimentin, Fibronectin, TWIST1, and SOX2 expression. NOTCH4 and HEY1 expression was associated with an EMT phenotype as well as increased invasion and cell migration.Conclusions: In HNSCC, the NOTCH4-HEY1 pathway is specifically upregulated, induces proliferation and cisplatin resistance, and promotes EMT. Clin Cancer Res; 24(3); 619-33. ©2017 AACR.
Insights
The NOTCH4-HEY1 pathway is activated in head and neck squamous cell carcinoma (HNSCC), driving cancer growth, resistance to cisplatin, and promoting epithelial-mesenchymal transition (EMT). This pathway is a potential therapeutic target for HNSCC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- NOTCH1 and NOTCH3 mutations are found in 20% of head and neck squamous cell carcinoma (HNSCC).
- The NOTCH pathway is implicated in HNSCC progression.
- The specific role of NOTCH4 in HNSCC remains unclear.
Purpose of the Study:
- To investigate the role of NOTCH4 in HNSCC.
- To analyze NOTCH4 pathway and downstream gene expression.
- To explore the functional impact of NOTCH4 on HNSCC cell behavior.
Main Methods:
- Analysis of TCGA dataset for NOTCH4 and downstream gene expression.
- In vitro assays for proliferation, cisplatin viability, apoptosis, and cell cycle.
- Comparison of NOTCH4, HEY1, and epithelial-mesenchymal transition (EMT)-related genes.
Main Results:
- HEY1 is upregulated in HNSCC compared to normal tissues.
- NOTCH4 significantly correlates with HEY1 activation in HNSCC.
- NOTCH4 promotes proliferation, cisplatin resistance, inhibits apoptosis, and disrupts cell cycle.
- NOTCH4 and HEY1 upregulate EMT markers (Vimentin, Fibronectin, TWIST1, SOX2) and decrease E-cadherin.
- NOTCH4 and HEY1 expression are linked to EMT, invasion, and migration.
Conclusions:
- The NOTCH4-HEY1 pathway is specifically upregulated in HNSCC.
- This pathway drives proliferation and cisplatin resistance.
- The NOTCH4-HEY1 pathway promotes epithelial-mesenchymal transition (EMT) in HNSCC.
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