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.

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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