Cancer Letters · 2019 · 40 citations · 41 references
MedicineOncologyPharmacologyApoptosisImmunotherapyMolecular OncologyApoptosis ResistanceCancer Stem Cell BiologyCancer Stem CellsChemotherapy ResistanceHer2-positive Breast CancerTargeted Cancer TherapyCancer Stem Cell - Mediated ResistanceCancer Stem Cell TargetingCancer Stem Cell-mediated ResistanceCancer Stem-like CellsTherapeutic Resistance MechanismsTrastuzumab ResistanceWee1 InhibitionWee1 Kinase Inhibition
Although trastuzumab has greatly improved the outcome of HER2-positive breast cancer, the emergence of resistance hampers its clinical benefits. Trastuzumab resistance is a multi-factorial consequence predominantly due to presence of cancer stem-like cells (CSCs). AZD1775, a potent anti-cancer agent targeting WEE1 kinase to drive tumor cells with DNA damage to premature mitosis, has previously shown high efficacies when targeting different cancers with a well-tolerated cytotoxic profile, but has not been evaluated in trastuzumab-resistant (TrR) breast cancer. We sought to investigate the effect of AZD1775 on cancer stem-like cell (CSC) properties, apoptosis, cell cycle regulation in TrR breast cancer. Our study for the first time demonstrated that AZD1775 induces apoptosis and arrests TrR cells at G2/M phase. More importantly, AZD1775 effectively targeted CSC properties by suppressing MUC1 expression levels. AZD1775 administration also induced apoptosis in our in-house patient-derived tumor cell line at passage 0, implying its significant clinical relevance. These findings highlight the potential clinical application of AZD1775 in overcoming trastuzumab resistance in breast cancer.
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