IndraLab
Statements
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"EGF could activate FAK and p130cas phosphorylation, while fibronectin could activate ERK general phosphorylation.The effect of EGFR mAbs and TKIs on gastric cancer cells Cetuximab, an IgG1 anti-EGFR mAb, can bind specially to the extracellular domain of EGFR on both normal and tumor cells, thus competitively inhibiting the binding of EGF [36]."
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"A recent study identified a splicing isoform of the SRC-3 oncogene, SRC-3Delta4, as a signaling adaptor that links epidermal growth factor receptor (EGFR) and FAK and promotes EGF induced phosphorylations of FAK and c-Src in the signaling cascade leading to epidermal growth factor (EGF)-induced cell migration, an event that requires mechanical signal co-ordination by FA."
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"However, ouabain inhibited EGF-induced activation of the Erk1/2 and Akt signaling pathways as well as p21 Ras activation, prevented EGF-induced formation of actin stress fibers, and inhibited EGF-induced FAK phosphorylation and DAOY cell motility, possibly through activation of stress signaling."
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"The above results suggested that EGF induced the phosphorylation of FAK (397 sites) in colorectal cancer cells, and the the downregulated expression or activity of FAK significantly inhibited EGF-induced EMT in colorectal cancer cells.After pretreatment with FAK inhibitor PF-228 (10 μM) for 1 hour, the migration and invasion abilities of EGF-induced colorectal cancer cells was determined by the transwell assay."