Expression of proton-sensing G-protein-coupled receptors in selected skin tumors

Exp Dermatol. 2019 Jan;28(1):66-71. doi: 10.1111/exd.13809. Epub 2018 Dec 13.

Abstract

Background: In humans, there are four known proton-sensing G-Protein-coupled receptors (pH-GPCRs): GPR4 (GPR19), TDAG8 (GPR65, T-cell death-associated gene 8), OGR1 (GPR68, ovarian cancer GPCR1) and G2A (GPR132, G2 accumulation protein). They are known to be involved in sensing changes of extracellular proton concentrations in the acidic microenvironment of tumors, which leads to altered cell proliferation, migration, metastasis, immune cell function and inflammation. However, little is known about the expression of pH-GPCRs in the skin and especially skin cancers.

Aim: We studied the expression of pH-GPCRs in selected skin cancers, that is Merkel cell carcinoma (MCC), dermatofibrosarcoma protuberans (DFSP), atypical fibroxanthoma (AFX) and pleomorphic dermal sarcoma (PDS).

Methods: We did immunohistochemistry and immunofluorescence to analyse the expression of GPR4, TDAG8, OGR1 and G2A using paraffin-embedded tissue samples (n = 4, exceptions: PDS GPR4/GPR65 n = 5, AFX GPR132 n = 3) from patients suffering from MCC, DFSP, AFX and PDS.

Results: (a) GPR4 was expressed on all AFX and PDS specimens. All AFX and MCC showed a positive expression of G2A. All PDS exhibited a strong positive expression of G2A. (b) MCCs neither expressed GPR4 nor TDAG8. All DFSP showed no expression of TDAG8. (c) For any other combination of GPCR and skin disease, we found positive/negative mixed results.

Conclusions: These are the first results on pH-GPCRs in selected skin cancers. We provide evidence that these GPCRs are differentially expressed on the various types of skin cancers and that they can potentially be addressed as a therapeutic target in extensive disease.

Keywords: atypical fibroxanthoma; dermatofibrosarcoma protuberans; merkel cell carcinoma; pleomorphic dermal sarcoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Merkel Cell / metabolism
  • Cell Cycle Proteins / metabolism
  • Cell Movement
  • Cell Proliferation
  • Dermatofibrosarcoma / metabolism
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Hydrogen-Ion Concentration
  • Immunohistochemistry
  • Inflammation
  • Microscopy, Fluorescence
  • Neoplasm Metastasis
  • Nerve Tissue Proteins / metabolism
  • Receptors, G-Protein-Coupled / metabolism*
  • Receptors, Neurotransmitter / metabolism
  • Sarcoma / metabolism
  • Skin Neoplasms / metabolism*
  • Tumor Microenvironment
  • Xanthomatosis / metabolism

Substances

  • Cell Cycle Proteins
  • G2A receptor
  • GPR19 protein, human
  • GPR65 protein, human
  • GPR68 protein, human
  • Nerve Tissue Proteins
  • Receptors, G-Protein-Coupled
  • Receptors, Neurotransmitter