COX-2 promotes colon cancer. While both nonselective NSAIDs and selective COX-2 inhibitors reduce disease burden, their adverse gastrointestinal and cardiovascular side effects limit their therapeutic use. In this issue of the JCI, Zhang et al. used gene silencing and a derivative of licorice root to show that inhibition of the enzyme 11β–hydroxysteroid dehydrogenase type II (11βHSD2) reduces tumor COX-2 activity, tumor growth, and metastasis by increasing the tonic glucocorticoid-mediated suppression of the COX-2 signaling pathway without the adverse effects associated with NSAIDs and selective COX-2 inhibitors (see the related article beginning on page 876). Their findings suggest that 11βHSD2 inhibition may be a potential therapeutic option in colon cancer, warranting further investigation.
Paul M. Stewart, Stephen M. Prescott
Title and authors | Publication | Year |
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Licochalcone-E induces caspase-dependent death of human pharyngeal squamous carcinoma cells through the extrinsic and intrinsic apoptotic signaling pathways
SJ Yu, IA Cho, KR Kang, YR Jung, S Cho, G Yoon, JS Oh, JS You, YS Seo, GJ Lee, SY Lee, D Kim, C Kim, SG Kim, MA Jeong, JS Kim |
Oncology Letters | 2017 |
Identification and characterization of a 20β-HSDH from the anaerobic gut bacterium Butyricicoccus desmolans ATCC 43058
S Devendran, C Méndez-García, JM Ridlon |
Journal of lipid research | 2017 |