期刊
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
卷 1859, 期 9, 页码 984-996出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbabio.2018.03.018
关键词
CSCs signalling; HMGR; Bergamot; Mevalonate pathway inhibitor; Rho-GDI-signalling; Breast cancer
Here, we show that a 2:1 mixture of Brutieridin and Melitidin, termed BMF, has a statin-like properties, which blocks the action of the rate-limiting enzyme for mevalonate biosynthesis, namely HMGR (3-hydroxy-3-methylglutaryl-CoA-reductase). Moreover, our results indicate that BMF functionally inhibits several key characteristics of CSCs. More specifically, BMF effectively i) reduced ALDH activity, ii) blocked mammosphere formation and iii) inhibited the activation of CSC-associated signalling pathways (STAT1/3, Notch and Wnt/beta-catenin) targeting Rho-GDI-signalling. In addition, BMF metabolically inhibited mitochondrial respiration (OXPHOS) and fatty acid oxidation (FAO). Importantly, BMF did not show the same toxic side-effects in normal fibroblasts that were observed with statins. Lastly, we show that high expression of the mRNA species encoding HMGR is associated with poor clinical outcome in breast cancer patients, providing a potential companion diagnostic for BMF-directed personalized therapy.
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