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Validated Immunochemical Assay for Comprehensive Determination of the Human Epidermal Growth Factor Receptor 2 Released from and Bound to Cells
Published on: May 9, 2025
HER2 and EGFR expression in cutaneous spindle squamous cell carcinoma
Scott M Schlauder1, Kenneth B Calder, Patricia Moody
1Department of Pathology, University of South Florida College of Medicine, Tampa, FL, USA. schlauders@yahoo.com
The American Journal of Dermatopathology
|November 23, 2007
Summary
Epidermal growth factor receptor (EGFR) and HER2 are not overexpressed in spindle squamous cell carcinoma (SSC). This finding aligns with SSC
Area of Science:
- Oncology
- Dermatopathology
- Molecular Biology
Background:
- Epidermal growth factor receptor (EGFR) and HER2 are transmembrane receptor tyrosine kinases (RTKs) involved in cell signaling and implicated in tumorigenesis.
- Approximately 80% of cutaneous squamous cell carcinomas (SCC) express EGFR, but expression in primary cutaneous spindle squamous cell carcinoma (SSC) is unstudied.
- RTK expression in extracutaneous spindle cell carcinomas is a prognostic indicator of potentially poor outcomes.
Purpose of the Study:
- To investigate the expression of EGFR and HER2 in primary cutaneous spindle squamous cell carcinoma (SSC).
- To evaluate the potential prognostic and therapeutic implications of EGFR and HER2 expression in SSC.
Main Methods:
- Retrieved 13 archival cases of primary nonmetastatic cutaneous SSC.
- Utilized immunohistochemistry to assess EGFR and HER2 expression.
- Confirmed all cases by a board-certified dermatopathologist prior to study.
Main Results:
- None of the 13 cases (0%) showed HER2 immunoreactivity.
- Only one case (<8%) demonstrated positive EGFR staining.
- EGFR and HER2 are not overexpressed in primary cutaneous SSC.
Conclusions:
- The lack of EGFR and HER2 overexpression in SSC supports the notion of its limited metastatic potential.
- Findings suggest variability in EGFR and HER2 expression among SCC histologic subtypes.
- This variability may have significant prognostic and therapeutic implications for SSC management.

