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von Breitenbuch, Philipp ; Kurz, Bernadett ; Wallner, Susanne ; Zeman, Florian ; Brochhausen, Christoph ; Schlitt, Hans-Jürgen ; Schreml, Stephan

Expression of pH-Sensitive GPCRs in Peritoneal Carcinomatosis of Colorectal Cancer—First Results

Artikel

von Breitenbuch, Philipp, Kurz, Bernadett, Wallner, Susanne, Zeman, Florian , Brochhausen, Christoph , Schlitt, Hans-Jürgen und Schreml, Stephan (2023) Expression of pH-Sensitive GPCRs in Peritoneal Carcinomatosis of Colorectal Cancer—First Results. Journal of Clinical Medicine 12 (5), S. 1803.

DOI zum Zitieren dieses Dokuments: 10.5283/epub.53899


Zusammenfassung

Solid tumors have an altered metabolism with a so-called inside-out pH gradient (decreased pH(e) < increased pH(i)). This also signals back to tumor cells via proton-sensitive ion channels or G protein-coupled receptors (pH-GPCRs) to alter migration and proliferation. Nothing, however, is known about the expression of pH-GPCRs in the rare form of peritoneal carcinomatosis. Paraffin-embedded ...

Solid tumors have an altered metabolism with a so-called inside-out pH gradient (decreased pH(e) < increased pH(i)). This also signals back to tumor cells via proton-sensitive ion channels or G protein-coupled receptors (pH-GPCRs) to alter migration and proliferation. Nothing, however, is known about the expression of pH-GPCRs in the rare form of peritoneal carcinomatosis. Paraffin-embedded tissue samples of a series of 10 patients with peritoneal carcinomatosis of colorectal (including appendix) origin were used for immunohistochemistry to study the expression of GPR4, GPR65, GPR68, GPR132, and GPR151. GPR4 was just expressed weakly in 30% of samples and expression was significantly reduced as compared to GPR56, GPR132, and GPR151. Furthermore, GPR68 was only expressed in 60% of tumors and showed significantly reduced expression as compared to GPR65 and GPR151. This is the first study on pH-GPCRs in peritoneal carcinomatosis, which shows lower expression of GPR4 and GPR68 as compared to other pH-GPCRs in this type of cancer. It may give rise to future therapies targeting either the TME or these GPCRs directly.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftJournal of Clinical Medicine
VerlagMDPI
Open Access ArtGold (mit APC - bezahlt UR)
Ort der VeröffentlichungBASEL
Band12
Nummer des Zeitschriftenheftes oder des Kapitels5
SeitenbereichS. 1803
Datum23 Februar 2023
Veröffentlichungsdatum06 Mrz 2023 16:28
InstitutionenMedizin > Lehrstuhl für Chirurgie
Medizin > Lehrstuhl für Dermatologie und Venerologie
Medizin > Lehrstuhl für Pathologie
Medizin > Zentren des Universitätsklinikums Regensburg > Zentrum für Klinische Studien
Identifikationsnummer
WertTyp
10.3390/jcm12051803DOI
Stichwörter / KeywordsPROTEIN-COUPLED RECEPTOR; TUMOR-GROWTH; TDAG8; MIGRATION; GENE; OVEREXPRESSION; PROLIFERATION; INVOLVEMENT; METASTASIS; INHIBITION; colorectal; peritoneal carcinomatosis; tumor microenvironment
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
URN der UB Regensburgurn:nbn:de:bvb:355-epub-538993
Dokumenten-ID53899

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