Furthermore, MTS assays showed that Mcl-1 knockdown (KD) significantly sensitized Hep3B and SNU475 cells to MLN2238 treatment compared with cells transfected with control siRNA (siNC), whereas although a reduction of cell viability was observed in HepG2 cells after Mcl-1 KD, differences did not reach statistical significance (Fig. 5c , right side).
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Preclinical evaluation of antitumor activity of the proteasome inhibitor MLN2238 (ixazomib) in hepatocellular carcinoma cells.
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