Irreversible inhibition of Δ16HER2 is necessary to suppress Δ16HER2-positive breast carcinomas resistant to Lapatinib
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文摘

Saracatinib and Dacomitinib block the oncogenic Δ16HER2/Src axis in vitro.

Erk signaling escape pathway mediates acquired resistance to Saracatinib in vivo.

Δ16HER2+ breast tumors are refractory to reversible TKI Lapatinib.

Δ16HER2+ breast tumors are responsive to irreversible TKI Dacomitinib.

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