Commentary 10.1172/JCI133115
1Navarra’s Health Research Institute (IDISNA) Pamplona, Spain.
2Program in Solid Tumors, Foundation for Applied Medical Research, Pamplona, Spain.
3Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
Address correspondence to: Marta M. Alonso, Department of Pediatrics, Clínica Universidad de Navarra, CIMA Building, Avd. Pio XII, 55 Pamplona, Spain. Phone: 34.948194700.1017; Email: mmalonso@unav.es.
Find articles by Iñigo-Marco, I. in: JCI | PubMed | Google Scholar
1Navarra’s Health Research Institute (IDISNA) Pamplona, Spain.
2Program in Solid Tumors, Foundation for Applied Medical Research, Pamplona, Spain.
3Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
Address correspondence to: Marta M. Alonso, Department of Pediatrics, Clínica Universidad de Navarra, CIMA Building, Avd. Pio XII, 55 Pamplona, Spain. Phone: 34.948194700.1017; Email: mmalonso@unav.es.
Find articles by Alonso, M. in: JCI | PubMed | Google Scholar
First published November 11, 2019 - More info
Tumor-induced immunosuppression is a common obstacle for cancer treatment. Adrenergic signaling triggered by chronic stress participates in the creation of an immunosuppressive microenvironment by promoting myeloid-derived suppressor cell (MDSC) proliferation and activation. In this issue of the JCI, Mohammadpour et al. elegantly delve into the mechanisms underlying MDSC contribution to tumor development. They used in vitro and in vivo mouse models to demonstrate that chronic stress results in MDSC accumulation, survival, and immune-inhibitory activity. Of therapeutic relevance, the authors showed that propranolol, a commonly prescribed β-blocker, can reduce MDSC immunosuppression and enhance the effect of other cancer therapies.
A subscription is required for you to read this article in full. If you are a subscriber, you may sign in to continue reading.
Click here to sign into your account.
Please select one of the subscription options, which includes a low-cost option just for this article.
If you are at an institution or library and believe you should have access, please check with your librarian or administrator (more information).
Please try these troubleshooting tips.