Journal Article

Targeting the endothelin axis as a therapeutic strategy for oral cancer metastasis and pain

King Chong Chan, Chi T. Viet, Yogin K. Patel, Johnny D. Figueroa, Kentaro Ono, Gary Yu, Bradley E. Aouizerat, Yi Ye, Coleen Doan, Dongmin Dang, Dan T. Viet

2020

Overview

Metastasis reduces survival in oral cancer patients and pain is their greatest complaint. We have shown previously that oral cancer metastasis and pain are controlled by the endothelin axis, which is a pathway comprised of the endothelin A and B receptors (ET A R and ET B R). In this study we focus on individual genes of the pathway, demonstrating that the endothelin axis genes are methylated and dysregulated in cancer tissue. Based on these findings in patients, we hypothesize that ET A R and ET B R play dichotomous roles in oral carcinogenesis and pain, such that ET A R activation and silenced ET B R expression result in increased carcinogenesis and pain. We test a treatment strategy that targets the dichotomous functions of the two receptors by inhibiting ET A R with macitentan, an ET A R antagonist approved for treatment of pulmonary hypertension, and re-expressing the ET B R gene with adenovirus transduction, and determine the treatment effect on cancer invasion (i.e., metastasis), proliferation and pain in vitro and in vivo. We demonstrate that combination treatment of macitentan and ET B R gene therapy inhibits invasion, but not proliferation, in cell culture and in a mouse model of tongue cancer. Furthermore, the treatment combination produces an antinociceptive effect through inhibition of endothelin-1 mediated neuronal activation, revealing the analgesic potential of macitentan. Our treatment approach targets a pathway shown to be dysregulated in oral cancer patients, using gene therapy and repurposing an available drug to effectively treat both oral cancer metastasis and pain in a preclinical model.

• Publisher: Springer Science and Business Media LLC,Nature Publishing Group UK,Nature Publishing Group
• Subject: 631/337/176 / 631/337/176/1988 / 631/337/176/2016 / 631/67 / 631/67/1059 / 631/67/1536 / 631/67/1665 / 692/1807/410 / Adult / Analgesics / Animals / Carcinogenesis / Cell culture / Cell Line, Tumor / Cell Proliferation / Cell Proliferation - genetics / Endothelin 1 / Endothelins / Endothelins - genetics / Endothelins - metabolism / Endothelins - physiology / Female / Gene therapy / HeLa Cells / Humanities and Social Sciences / Humans / Hypertension / Male / Metastases / Metastasis / Mice / Mice, Inbred BALB C / Mouth Neoplasms / Mouth Neoplasms - metabolism / Mouth Neoplasms - therapy / multidisciplinary / Neoplasm Invasiveness / Neoplasm Invasiveness - genetics / Neoplasm Metastasis / Neoplasm Metastasis - therapy / Oral cancer / Pain / Pain - metabolism / Pain - physiopathology / Pain Management / Pain Management - methods / Pain perception / Pyrimidines / Pyrimidines - pharmacology / Receptor, Endothelin A / Receptor, Endothelin A - genetics / Receptor, Endothelin A - metabolism / Receptor, Endothelin B / Receptor, Endothelin B - genetics / Receptor, Endothelin B - metabolism / Science / Science (multidisciplinary) / Sulfonamides / Sulfonamides - pharmacology