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Expression profiles of proton-sensing G-protein coupled receptors in common skin tumors
Klatt, Wybke, Wallner, Susanne, Brochhausen, Christoph
, Stolwijk, Judith A. und Schreml, Stephan
(2020)
Expression profiles of proton-sensing G-protein coupled receptors in common skin tumors.
Scientific Reports 10, S. 15327.
Veröffentlichungsdatum dieses Volltextes: 23 Feb 2021 10:10
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.45050
Zusammenfassung
The proton-sensing GPCRs (pH-GPCRs) GPR4 (GPR19), TDAG8 (GPR65, T-cell death associated gene 8), OGR1 (GPR68, ovarian cancer GPCR1), and G2A (GPR132, G2 accumulation protein) are involved in sensing and transducing changes in extracellular pH (pH(e)). Extracellular acidification is a central hallmark of solid cancer. pH-GPCR function has been associated with cancer cell proliferation, adhesion, ...
The proton-sensing GPCRs (pH-GPCRs) GPR4 (GPR19), TDAG8 (GPR65, T-cell death associated gene 8), OGR1 (GPR68, ovarian cancer GPCR1), and G2A (GPR132, G2 accumulation protein) are involved in sensing and transducing changes in extracellular pH (pH(e)). Extracellular acidification is a central hallmark of solid cancer. pH-GPCR function has been associated with cancer cell proliferation, adhesion, migration and metastasis, as well as with modulation of the immune system. Little is known about the expression levels and role of pH-GPCRs in skin cancer. To better understand the functions of pH-GPCRs in skin cancer in vivo, we examined the expression-profiles of GPR4, TDAG8, OGR1 and G2A in four common skin tumors, i.e. squamous cell carcinoma (SCC), malignant melanoma (MM), compound nevus cell nevi (NCN), basal cell carcinoma (BCC). We performed immunohistochemistry and immunofluorescence staining on paraffin-embedded tissue samples acquired from patients suffering from SCC, MM, NCN or BCC. We show the expression of pH-GPCRs in four common skin cancers. Different expression patterns in the investigated skin cancer types indicate that the different pH-GPCRs may have distinct functions in tumor progression and serve as novel therapeutic targets.
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| Dokumentenart | Artikel | ||||
| Titel eines Journals oder einer Zeitschrift | Scientific Reports | ||||
| Verlag: | Nature | ||||
|---|---|---|---|---|---|
| Ort der Veröffentlichung: | BERLIN | ||||
| Band: | 10 | ||||
| Seitenbereich: | S. 15327 | ||||
| Datum | 18 September 2020 | ||||
| Institutionen | Medizin > Lehrstuhl für Dermatologie und Venerologie Medizin > Lehrstuhl für Pathologie Chemie und Pharmazie > Institut für Analytische Chemie, Chemo- und Biosensorik | ||||
| Identifikationsnummer |
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| Stichwörter / Keywords | EXTRACELLULAR ACIDIFICATION; PH; TDAG8; OGR1; GENE; G2A; MIGRATION; GPR4; PROLIFERATION; INFLAMMATION; | ||||
| Dewey-Dezimal-Klassifikation | 500 Naturwissenschaften und Mathematik > 540 Chemie 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin | ||||
| Status | Veröffentlicht | ||||
| Begutachtet | Ja, diese Version wurde begutachtet | ||||
| An der Universität Regensburg entstanden | Ja | ||||
| URN der UB Regensburg | urn:nbn:de:bvb:355-epub-450509 | ||||
| Dokumenten-ID | 45050 |
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