APBB1 reinforces cancer stem cell and epithelial-to-mesenchymal transition by regulating the IGF1R signaling pathway in non-small-cell lung cancer cells.
Amyloid β precursor protein binding family B member 1(APBB1) was first identified as a binding partner of amyloid precursor protein during brain development, but its function in the context of cancer remain unclear. Here we show for the first time that APBB1 is partly associated with intensifying cancer stem cell(CSC) ... and epithelial-to-mesenchymal transition (EMT) and enhancing radiation-resistant properties of lung cancer cells. We found that APBB1 was highly expressed in ALDH1high CSC-like cells sorted from A549 lung cancer cells. In APBB1-deficient H460 cells with forced overexpression of APBB1, the protein directly interacted with IGF1Rβ, enhanced phosphorylation of IGF1Rβ/PI3K/AKT pathway(activation) and subsequently induced the phosphorylation of GSK3β(inactivation). This phosphorylation stabilized Snail1, a negative regulator of E-cadherin expression, and regulated β-catenin-mediated ALDH1 expression, which are representative markers for EMT and CSCs, respectively. In contrast, suppression of APBB1 expression with siRNA yielded the opposite effects in APBB1-rich A549 cells. We concluded that APBB1 partly regulates the expression of ALDH1. We also found that APBB1 regulates activation of nuclear factor-κB, which is involved in reducing various stresses including oxidative stress, which suggests that APBB1 is associated with γ-radiation sensitivity. Our findings imply that APBB1 plays an important role in the maintenance of EMT-associated CSC-like properties and γ-radiation resistance via activation of IGF1Rβ/AKT/GSK3β pathway in lung cancer cells, highlighting APBB1 as a potential target for therapeutic cancer treatment.
Mesh Terms:
A549 Cells, Carcinoma, Non-Small-Cell Lung, Cell Line, Tumor, Dose-Response Relationship, Radiation, Epithelial-Mesenchymal Transition, Gene Expression Regulation, Neoplastic, Humans, Neoplastic Stem Cells, Nerve Tissue Proteins, Nuclear Proteins, Radiation Tolerance, Radiotherapy Dosage, Receptors, Somatomedin, Signal Transduction
A549 Cells, Carcinoma, Non-Small-Cell Lung, Cell Line, Tumor, Dose-Response Relationship, Radiation, Epithelial-Mesenchymal Transition, Gene Expression Regulation, Neoplastic, Humans, Neoplastic Stem Cells, Nerve Tissue Proteins, Nuclear Proteins, Radiation Tolerance, Radiotherapy Dosage, Receptors, Somatomedin, Signal Transduction
Biochem. Biophys. Res. Commun.
Date: Jan. 01, 2017
PubMed ID: 27836546
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