Dopamine Prevents Ultraviolet B–induced Development and Progression of Premalignant Cutaneous Lesions through its D2 Receptors

Abstract

Although the role of dopamine (DA) in malignant tumors has been reported, its function in premalignant lesions is unknown. Herein we report that the stimulation of DA D2 receptors in endothelial cells in ultraviolet B (UVB)-induced cutaneous lesions in mice significantly reduced the tumor number, tumor burden, and malignant squamous cell carcinoma in these animals. DA D2 receptor agonist inhibited VEGFA-dependent proangiogenic genes in vitro and in vivo. However, the mice pretreated with selective DA D2 receptor antagonist inhibited the actions of the agonist, thereby suggesting that the action of DA was through its D2 receptors in the endothelial cells. To our knowledge, this study is the first to report DA-mediated regulation of pathogenesis and progression of UVB-induced premalignant skin lesions.

Document Details

Document Type
Pub Defense Publication
Publication Date
Apr 12, 2021
Source ID
10.1158/1940-6207.capr-21-0052

Entities

People

  • Kai Lu
  • Madhavi Bhat
  • Partha Sarathi Dasgupta
  • Rita Mitra
  • Sara Peters
  • Sujit Basu
  • Tatiana M. Oberyszyn
  • Xiaokui Mo

Organizations

  • Blueprint for Neuroscience Research
  • Ohio State University
  • United States Department of Defense

Tags

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology and Pathology
  • Neurodegenerative Parkinson's Disease and Rickettsial Disease handbook, including the data level of dopamine, BC, neurons, and PD.
  • Oncology (Cancer Research).