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Different serotonergic expression in nevomelanocytic tumors
Clara Naimi-Akbar1, Markus Ritter, Sasika Demel
1Dermatology and Venereology Unit, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Solna, Sweden. klas.nordlind@karolinska.se.
Cancers
|November 28, 2013
Summary
Serotonin (5-hydroxytryptamine; 5-HT) system alterations are present in nevomelanocytic tumors, including melanoma. Mast cells expressing serotonin markers may play a role in tumor progression.
Area of Science:
- Oncology
- Neuroscience
- Dermatology
Background:
- Serotonin (5-hydroxytryptamine; 5-HT) is implicated in tumor progression.
- The role of the serotonergic system in nevomelanocytic tumors requires further investigation.
Purpose of the Study:
- To investigate alterations in the serotonergic system within nevomelanocytic tumors.
- To determine the expression of serotonin, 5-HT1A receptors, 5-HT2A receptors, and the serotonin transporter protein (SERT) in benign nevi, dysplastic nevi, and malignant melanoma.
Main Methods:
- Immunohistochemical analysis of paraffin-embedded biopsies from benign compound nevi (BCN), dysplastic compound nevi (DN), and superficial spreading malignant melanoma (SSM).
- Characterization of 5-HT, 5-HT1A receptors (5-HT1AR), 5-HT2A receptors (5-HT2AR), and SERT expression in tumor cells and surrounding melanocytes.
Main Results:
- Melanocytes surrounding tumors expressed 5-HT1AR and 5-HT2AR.
- DN and SSM tissues showed positive immunostaining for serotonergic markers in suprabasal epidermis, more pronounced in SSM.
- Decreased 5-HT1AR expression at the junctional area in SSM compared to DN and BCN.
- Reduced dermal 5-HT1AR and SERT staining intensity with increasing atypia.
- Increased vessel immunoreactivity for 5-HT2A in SSM versus BCN.
- Tryptase-positive mast cells expressing SERT and 5-HT1AR were observed infiltrating dermal regions of DN and SSM.
Conclusions:
- Alterations in the serotonergic system are associated with nevomelanocytic tumors.
- Mast cells expressing serotonergic markers may contribute to tumor progression in melanoma and dysplastic nevi.

