Additionally, whilst the combination of PPP and OX (53 μM) led to a reduction in migration in HCT116 cells compared with OX alone, this decrease did not reach statistical significance.
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Picropodophyllin, an IGF‑1 receptor inhibitor, enhances oxaliplatin efficacy in chemoresistant colorectal cancer HCT116 cells by reducing metastatic potential.
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As EMT serves a crucial role in acquired resistance, there is an increasing trend towards agents that increase treatment sensitivity by targeting EMT inhibition ( 16 , 43 – 45 ).
Whilst the higher concentration of OX (324 μM) combined with PPP (1 μM) showed a trend toward greater cytotoxicity in resistant cells, this difference was not statistically significant.