P2X1 and P2X7 Receptor Overexpression Is a Negative Predictor of Survival in Muscle-Invasive Bladder Cancer

Author:

Ledderose Stephan1,Rodler Severin2ORCID,Eismann Lennert2ORCID,Ledderose Georg3ORCID,Rudelius Martina1,Junger Wolfgang G.45,Ledderose Carola45ORCID

Affiliation:

1. Institute of Pathology, Ludwig Maximilian University, 80337 Munich, Germany

2. Department of Urology, Ludwig Maximilian University, 81377 Munich, Germany

3. Department of Oto-Rhino-Laryngology, Ludwig Maximilian University, 81377 Munich, Germany

4. Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA

5. Department of Surgery, University of California San Diego Health, La Jolla, CA 92037, USA

Abstract

Bladder cancer is amongst the most common causes of cancer death worldwide. Muscle-invasive bladder cancer (MIBC) bears a particularly poor prognosis. Overexpression of purinergic P2X receptors (P2XRs) has been associated with worse outcome in several malignant tumors. Here, we investigated the role of P2XRs in bladder cancer cell proliferation in vitro and the prognostic value of P2XR expression in MIBC patients. Cell culture experiments with T24, RT4, and non-transformed TRT-HU-1 cells revealed a link between high ATP concentrations in the cell culture supernatants of bladder cell lines and a higher grade of malignancy. Furthermore, proliferation of highly malignant T24 bladder cancer cells depended on autocrine signaling through P2X receptors. P2X1R, P2X4R, and P2X7R expression was immunohistochemically analyzed in tumor specimens from 173 patients with MIBC. High P2X1R expression was associated with pathological parameters of disease progression and reduced survival time. High combined expression of P2X1R and P2X7R increased the risk of distant metastasis and was an independent negative predictor of overall and tumor-specific survival in multivariate analyses. Our results suggest that P2X1R/P2X7R expression scores are powerful negative prognostic markers in MIBC patients and that P2XR-mediated pathways are potential targets for novel therapeutic strategies in bladder cancer.

Funder

Bavarian Center for Cancer Research

Friedrich Baur Foundation

National Institutes of Health

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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