1. Academic Validation
  2. Characterization of the Olfactory Receptor OR10H1 in Human Urinary Bladder Cancer

Characterization of the Olfactory Receptor OR10H1 in Human Urinary Bladder Cancer

  • Front Physiol. 2018 May 16;9:456. doi: 10.3389/fphys.2018.00456.
Lea Weber 1 2 Wolfgang A Schulz 3 Stathis Philippou 4 Josephine Eckardt 1 5 Burkhard Ubrig 6 Michéle J Hoffmann 3 Andrea Tannapfel 7 Benjamin Kalbe 1 Günter Gisselmann 1 Hanns Hatt 1
Affiliations

Affiliations

  • 1 Department of Cellular Physiology, Ruhr University Bochum, Bochum, Germany.
  • 2 Department of Translational Wound Research, Witten/Herdecke University, Witten, Germany.
  • 3 Department of Urology, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • 4 Department of Pathology and Cytology, Augusta Kliniken Bochum Hattingen, Bochum, Germany.
  • 5 Institute for Physiology, Ruhr University Bochum, Bochum, Germany.
  • 6 Clinic for Urology, Augusta Kliniken Bochum Hattingen, Bochum, Germany.
  • 7 Institute for Pathology, Ruhr University Bochum, Bochum, Germany.
Abstract

Olfactory receptors (ORs) are a large group of G-protein coupled receptors predominantly found in the olfactory epithelium. Many ORs are, however, ectopically expressed in other tissues and involved in several diseases including Cancer. In this study, we describe that one OR, OR10H1, is predominantly expressed in the human urinary bladder with a notably higher expression at mRNA and protein level in bladder Cancer tissues. Interestingly, also significantly higher amounts of OR10H1 transcripts were detectable in the urine of bladder Cancer patients than in the urine of control persons. We identified the sandalwood-related compound Sandranol as a specific agonist of OR10H1. This deorphanization allowed the functional characterization of OR10H1 in BFTC905 bladder Cancer cells. The effect of receptor activation was morphologically apparent in cell rounding, accompanied by changes in the Cytoskeleton detected by β-actin, T-cadherin and β-catenin staining. In addition, Sandranol treatment significantly diminished cell viability, cell proliferation and migration and induced a limited degree of Apoptosis. Cell cycle analysis revealed an increased G1 fraction. In a concentration-dependent manner, Sandranol application elevated cAMP levels, which was reduced by inhibition of adenylyl cyclase, and elicited intracellular Ca2+ concentration increase. Furthermore, activation of OR10H1 enhanced secretion of ATP and serotonin. Our results suggest OR10H1 as a potential biomarker and therapeutic target for bladder Cancer.

Keywords

OR10H1; biomarker; bladder; bladder cancer; next generation sequencing; olfactory receptor.

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