IndraLab

Statements


USP13 activates mutated EGFR. 5 / 5
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"37 USP13 is likely to stabilize mutant EGFR in a ubiquitinated state, and inhibition of USP13 destabilizes mutant EGFR and abrogates signaling of mutant EGFR in lung cancer cells."

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"Targeting USP13 mediated drug tolerance increases the efficacy of EGFR inhibition of mutant EGFR in non small cell lung cancer."

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"We found that USP13 inhibits mutant EGFR degradation by a process that leads to the accumulation of ubiquitinated (K48 and K63) EGFR, which is bound to c-Cbl and USP13."

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"Combined targeting of USP13 and EGFR strongly reduces the viability of EGFR mutant lung cancer cells in vitro and in vivo while sparing non malignant (EGFR wild-type) lung epithelial cells."

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"Targeting USP13 increased the sensitivity of EGFRm NSCLC cells to EGFR inhibition with small molecules in vitro and in vivo, suggesting that USP13 is a strong mutant EGFR-specific co-target that could improve the treatment efficacy of EGFR-targeted therapies."