2019
DOI: 10.1016/j.ejmech.2018.12.029
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Translational impact of novel widely pharmacological characterized mofezolac-derived COX-1 inhibitors combined with bortezomib on human multiple myeloma cell lines viability

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Cited by 13 publications
(6 citation statements)
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“…The apoptotic rate of the cells treated with bortezomib was significantly higher than that of the untreated control group (P<0.05), which also showed that bortezomib has the effect of promoting myeloma cell apoptosis. These results are consistent with previous studies ( 26 , 27 ). Finally, the expression levels of Wnt/β-catenin signaling pathway-related proteins β-catenin and c-Myc were detected in each group by two methods.…”
Section: Discussionsupporting
confidence: 94%
“…The apoptotic rate of the cells treated with bortezomib was significantly higher than that of the untreated control group (P<0.05), which also showed that bortezomib has the effect of promoting myeloma cell apoptosis. These results are consistent with previous studies ( 26 , 27 ). Finally, the expression levels of Wnt/β-catenin signaling pathway-related proteins β-catenin and c-Myc were detected in each group by two methods.…”
Section: Discussionsupporting
confidence: 94%
“…COX catalyzes the first step in the biosynthesis of prostaglandins (PG), prostacyclin and thromboxane starting from free arachidonic acid (AA) [ 43 ]. Among prostaglandins, PGE 2 is involved in inflammation, angiogenesis and in promoting the growth of several solid tumors, such as breast, ovarian, head and neck cancer, renal cell carcinoma and hematological cancers [ 44 , 45 , 46 ]. COX-1 and COX-2 are of great interest because they are targets of non–steroidal anti–inflammatory drugs (NSAIDs), which, when binding to the active site of COX, prevent the AA from reaching the catalytic pocket and, thus, the biosynthesis of prostaglandins.…”
Section: Discussionmentioning
confidence: 99%
“…The western blotting analysis was conducted by using the methods reported in Perrone et al with minor modifications [38]. Briefly, all cells were washed twice with 10 mL phosphate-buffered saline (PBS), scraped in 1 mL PBS and centrifuged for 10 min at 1500 rpm, 4 • C. Proteins were extracted from cells by homogenization in cold RIPA buffer (Sigma-Aldrich) containing 1X protease inhibitor cocktail and centrifuged at 14,000 rpm for 10 min at 4 • C. The supernatant was recovered, and the protein concentration was measured using a DC Protein Assay Reagent Kit (BIO-RAD, Hercules, CA, USA).…”
Section: Western Blottingmentioning
confidence: 99%