Resistance to BET Bromodomain Inhibitors Is Mediated by Kinome Reprogramming in Ovarian Cancer
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文摘

Inhibition of BET proteins reprograms kinome activity in ovarian cancer cells

Receptor tyrosine kinase activation overcomes BET inhibition, causing resistance

Elevated PI3K/ERK activity stabilizes MYC/FOSL1 proteins in JQ1-resistant cells

Co-targeting BET proteins and RTK or PI3K signaling enhances BET inhibitor therapy

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