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Expression of Proton-Sensitive GPR31, GPR151, TASK1 and TASK3 in Common Skin Tumors
- Source :
- Cells, Cells; Volume 11; Issue 1; Pages: 27, Cells, Vol 11, Iss 27, p 27 (2022)
- Publication Year :
- 2021
- Publisher :
- MDPI, 2021.
-
Abstract
- TWIK-related acid-sensitive potassium channels TASK1 and TASK3, as well as the G-protein-coupled receptors GPR31 and GPR151, are proton-sensitive membrane proteins. They can be activated or inhibited by low extracellular pH (pHe), which is a hallmark of the tumor microenvironment in solid tumors. However, the role of these channels in the development of skin tumors is still unclear. In this study, we investigated the expression profiles of TASK1, TASK3, GPR31 and GPR151 in squamous cell carcinomas (SCCs), basal cell carcinomas (BCCs), nevus cell nevi (NCN), and malignant melanomas (MMs). We performed immunohistochemistry using paraffin-embedded tissue samples from patients and found that most skin tumors express TASK1/3 and GPR31/151. The results show that BCCs are often negative for GPR31/151 as well as for TASK1/3, while nearly all SCCs express these markers. MMs and NCN show similar expression patterns. However, some tumors show a decreasing TASK1/3 expression in deeper dermal tumor tissue, while GPCRs were expressed more evenly. The lower frequency of GPR31/151 and TSAK1/3 expression in BCCs when compared to SCCs is a novel histological feature distinguishing these two entities. Moreover, BCCs also show lower expression of GPR31/151 and TASK1/3 as compared to NCN and MMs.
- Subjects :
- Aged, 80 and over
Male
ddc:610
Skin Neoplasms
QH301-705.5
GPCR31/151
610 Medizin
Nerve Tissue Proteins
General Medicine
skin tumors
Middle Aged
TASK1/3
Task1/3
Article
Receptors, G-Protein-Coupled
Potassium Channels, Tandem Pore Domain
Carcinoma, Basal Cell
Cell Line, Tumor
Carcinoma, Squamous Cell
Humans
Female
Biology (General)
Protons
Aged
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Cells, Cells; Volume 11; Issue 1; Pages: 27, Cells, Vol 11, Iss 27, p 27 (2022)
- Accession number :
- edsair.doi.dedup.....3b38afc4b2d4413f0e6aeb20d5c2d90b