作者: Feng Gao , Tao Wang , Zefeng Zhang , Rui Wang , Yang Guo
DOI: 10.1007/S13277-015-3866-4
关键词: Translation (biology) 、 Lung cancer 、 Cancer 、 non-small cell lung cancer (NSCLC) 、 PI3K/AKT/mTOR pathway 、 Messenger RNA 、 Cell 、 Medicine 、 Pathology 、 Cancer research 、 Transforming growth factor
摘要: Activating protein-4 (AP4) has been recently shown to regulate the cancer metastases in some cancers including non-small cell lung (NSCLC). Specifically, AP4 regulates mTor/p21 and transforming growth factor β (TGFβ) receptor signaling pathway increase an epithelial-mesenchymal transition process augment invasiveness. Nevertheless, how is regulated NSCLC not studied. Here, we showed that specimens from patients, levels of miR-144 were significantly decreased increased, compared paired non-tumor tissue. The inversely correlated patients’ specimens. Bioinformatics analyses revealed targeted 3′-UTR mRNA inhibit its translation, confirmed by luciferase-reporter assay. Moreover, overexpression inhibited AP4-mediated invasiveness, while depletion increased invasiveness cells. Together, our data suggest suppression may be cause AP4, as well augmented metastases, NSCLC.