2016
DOI: 10.1016/j.yexcr.2016.05.023
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Resistance to ursolic acid-induced apoptosis through involvement of melanogenesis and COX-2/PGE2 pathways in human M4Beu melanoma cancer cells

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Cited by 16 publications
(8 citation statements)
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“…This protein is responsible for the production of inflammatory prostaglandins. Upregulation of COX2 is also associated with increased cell adhesion, phenotypic changes, resistance to apoptosis, and tumor angiogenesis [24, 25]. …”
Section: Discussionmentioning
confidence: 99%
“…This protein is responsible for the production of inflammatory prostaglandins. Upregulation of COX2 is also associated with increased cell adhesion, phenotypic changes, resistance to apoptosis, and tumor angiogenesis [24, 25]. …”
Section: Discussionmentioning
confidence: 99%
“…UA can be used as a potential therapeutic agent for the treatment of various cancers [281][282][283][284][285][286][287][288][289]. It induces apoptosis through both extrinsic death receptor and mitochondrial death pathways in human breast cancer MDA-MB-231 cells [289], and inhibits cell proliferation and induces pro-apoptosis in human breast cancer MCF-7 cells by FoxM1 inhibition [282].…”
Section: Ursolic Acid (Ua)mentioning
confidence: 99%
“…Many studies have pointed out that ursolic acid possesses potent anti-melanoma activity, correlated with modulation of different pathways, including NF-κB, p53, Akt and ERK1/2 proteins, and with caspase cascade activation [288][289][290][291][292]. Notably, it has also been demonstrated that tyrosinase-and TRP-1-mediated melanogenesis and COX-2/PGE2 pathway are implicated in the resistance of melanoma cells to the ursolic acid cytotoxicity [293,294].…”
Section: Ursolic Acidmentioning
confidence: 99%