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Updated: Feb 25, 2026

Merkel Cell Polyomavirus Infection and Detection
Published on: February 7, 2019
Tropomyosin Receptor Kinase A Expression on Merkel Cell Carcinoma Cells
Ulrike Wehkamp1, Sophie Stern1, Sandra Krüger2
1Department of Dermatology, University Hospital Schleswig-Holstein, Kiel, Germany.
Importance:
Merkel cell carcinoma (MCC) is a malignant neuroendocrine skin tumor frequently associated with the Merkel cell polyomavirus. Immune checkpoint therapy showed remarkable results, although not all patients are responsive to this therapy. Anti-tropomyosin receptor kinase A (TrkA)-targeted treatment has shown promising results in several tumor entities.
Objective:
To determine TrkA expression in MCC as a rationale for potential targeted therapy.
Design, Setting, And Participants:
This case series study investigated the MCC specimens of 55 patients treated at the Department of Dermatology, University Hospital of Schleswig-Holstein, Kiel, Germany, from January 1, 2005, through December 31, 2015. Thirty-nine of the 55 samples were suitable for further histopathologic examination. Expression of TrkA was explored by immunohistochemical analysis.
Exposure:
Diagnosis of MCC was confirmed by staining positive for cytokeratin 20 (CK20) and synaptophysin.
Main Outcomes And Measures:
Expression of TrkA on the tumor cells.
Results:
Specimens of 39 patients (21 women and 18 men; mean [SD] age, 75.0 [7.8] years) underwent immunohistochemical investigation. Thirty-eight of 38 specimens expressed CK20 and synaptophysin on the MCC tumor cells (100% expression). Merkel cell polyomavirus was detected in 32 of 38 specimens (84%). Tropomyosin receptor kinase A was found in all 36 evaluable specimens on the tumor cells; 34 (94%) showed a weak and 2 (6%) showed a strong cytoplasmic expression. In addition, strongly positive perinuclear dots were observed in 30 of 36 specimens (83%).
Conclusions And Relevance:
Tropomyosin receptor kinase A was expressed on MCC tumor cells in 100% of evaluable specimens. This result may lead to the exploration of new targeted treatment options in MCC, especially for patients who do not respond to anti-programmed cell death protein 1 treatment.
Insights
Tropomyosin receptor kinase A (TrkA) is expressed in all Merkel cell carcinoma (MCC) tumor cells. This finding supports TrkA as a potential therapeutic target for MCC, particularly for patients unresponsive to current immunotherapies.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine skin cancer.
- While immune checkpoint inhibitors have shown efficacy, a significant portion of patients do not respond.
- Tropomyosin receptor kinase A (TrkA) targeted therapy is emerging as a promising approach in various cancers.
Purpose of the Study:
- To investigate the expression of TrkA in Merkel cell carcinoma (MCC) specimens.
- To evaluate the potential of TrkA as a therapeutic target for MCC.
Main Methods:
- A case series study involving 55 MCC patients.
- Immunohistochemical analysis was performed on 39 suitable tumor specimens.
- TrkA expression was assessed on tumor cells, alongside diagnostic markers CK20 and synaptophysin.
Main Results:
- All 36 evaluable MCC specimens (100%) showed TrkA expression on tumor cells.
- Weak cytoplasmic expression was observed in 94% of cases, with strong expression in 6%.
- Positive perinuclear dots were noted in 83% of specimens.
Conclusions:
- Tropomyosin receptor kinase A (TrkA) is ubiquitously expressed in Merkel cell carcinoma (MCC) tumor cells.
- This high expression rate suggests TrkA as a potential therapeutic target for MCC.
- TrkA-targeted therapy could offer new treatment avenues for patients resistant to immune checkpoint inhibitors.
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