EMBO Molecular Medicine · 2013 · 191 citations · 34 references
MedicineImmunologyOncologyMetastasisMolecular OncologySignal TransductionCancer Stem Cell BiologyCancer Stem CellsMalignant NeoplasmsMetastatic Breast CancerMetastatic Signaling PathwaysNotch SignalingCancer Stem-like CellsMetastatic Breast Cancer BiologyMetastatic Cancer Stem CellsMetastatic MechanismsMetastatic SignalingNotch Receptor SignalingNotch ReceptorsNotch Signaling Activation
Brain metastasis of breast cancer profoundly affects the cognitive and sensory functions as well as morbidity of patients, and the 1 year survival rate among these patients remains less than 20%. However, the pathological mechanism of brain metastasis is as yet poorly understood. In this report, we found that metastatic breast tumour cells in the brain highly expressed IL-1β which then 'activated' surrounding astrocytes. This activation significantly augmented the expression of JAG1 in the astrocytes, and the direct interaction of the reactivated astrocytes and cancer stem-like cells (CSCs) significantly stimulated Notch signalling in CSCs. We also found that the activated Notch signalling in CSCs up-regulated HES5 followed by promoting self-renewal of CSCs. Furthermore, we have shown that the blood-brain barrier permeable Notch inhibitor, Compound E, can significantly suppress the brain metastasis in vivo. These results represent a novel paradigm for the understanding of how metastatic breast CSCs re-establish their niche for their self-renewal in a totally different microenvironment, which opens a new avenue to identify a novel and specific target for the brain metastatic disease.
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