The research was published in the International Journal of Molecular Sciences on June 8.
The lab study led by Luksana Chaiswing, Ph.D., assistant professor in the U.K. College of Medicine’s Department of Toxicology and Cancer Biology, is the first to demonstrate that betamethasone protects normal prostate cells from injury induced by radiation therapy, while making the cancer cells more susceptible to the treatment.
Prostate cancer is the second leading cause of cancer deaths among men in the U.S. While radiation therapy is important to control the growth of prostate cancer, it presents a significant risk of increasing unwanted side effects, including injury to normal tissues.
The team screened around 700 Food and Drug Administration-approved drugs for properties including protecting non-cancer cells against radiation therapy induced cytotoxicity, killing prostate cancer cells and increasing hydrogen peroxide levels in both cancer and non-cancer cells.
Betamethasone increases hydrogen peroxide levels, which activates a protective protein called “RelB” in normal, non-cancerous prostate cells.
More information: Luksana Chaiswing et al, The RelB-BLNK Axis Determines Cellular Response to a Novel Redox-Active Agent Betamethasone during Radiation Therapy in Prostate Cancer, International Journal of Molecular Sciences (2022). DOI: 10.3390/ijms23126409