
IndraLab
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USP33 activates Neoplasm Invasiveness. 19 / 19
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"As shown in Fig. 3A, compared with other ECM components, the binding ability of USP33-overexpressed cells was significantly increased in the laminin (which is also the primary component of Matrigel) group, indicating that USP33-mediated invasion may be related to the inducement of the adhesiveness to laminin."
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"To assess whether USP33 affected the invasiveness and migration of PC cells, we performed the transwell migration and invasion assays and found that USP33 knockdown significantly inhibited the migration and invasiveness of PC cells while USP33 overexpression showed the opposite effect (Fig. 2H–J)."
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"On the other hand, USP33 knock-down promoted cell proliferation and invasion under SDF-1 stimulation; whereas dynasore (an internalization inhibitor) pretreatment in USP33 silencing cells showed a distinct antipromoting effect, revealing the participation of CXCR4 internalization in regulating tumor progress."