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 know...
http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
https://www.riss.kr/link?id=O119120576
2019년
-
0906-6705
1600-0625
SCI;SCIE;SCOPUS
학술저널
66-71 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
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 know...
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.
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).
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.
(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.
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.
Antitumor activity of sulforaphane in mice model of skin cancer via blocking sulfatase‐2
CCN proteins as potential actionable targets in scleroderma