lation by acid alone ( Figure 3 , Supplemental Table S3 ) Treatment with 10 μM amprenavir led to statistically significant reductions in pH4 pepsin-mediated induction of MMP1 ( p = 0.0006), MMP7 ( p = 0.043), MMP9 ( p = 0.0066), and MMP14 ( p = 0.034), as well as a reduction in MMP2 expression that did not reach statistical significance ( p = 0.077).
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The Protease Inhibitor Amprenavir Protects against Pepsin-Induced Esophageal Epithelial Barrier Disruption and Cancer-Associated Changes.
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