DNA and Cell Biology · 2016 · 22 citations · 21 references
MedicineMolecular BiologyOncologyMetastasisMolecular OncologyTumor ProgressionCancer ProgressionLung CancerLung MetastasisMalignant NeoplasmsMicrorna-mediated RegulationTumor Suppressor GenesCell Viability AssaysMalignant ProgressionMicrorna Function In CancerMicrorna In CancerMicrorna ModulationMicrorna Regulation In CancerMicrorna-mediated OncogenesisReal-time Polymerase Chain Reaction (Pcr)
Lung cancer is one of the most malignant cancers with a high metastatic potential. The purpose of this study was to study the role and the underlying mechanism of miR-214 in lung cancer progression. The expression of miR-214 in normal lung and lung cancer tissue was analyzed by quantitative real-time PCR analysis. Furthermore, H1299 cells were infected with miR-214 lentivirus, and the effect of infection on cell viability and migration was analyzed. Carboxypeptidase-D (CPD), as a potential target of miR-214, was characterized in either normal lung or lung cancer tissues. The interaction of CPD expression with the tumor suppressing effect of miR-214 was characterized. We demonstrated that low miR-214 expression is a hallmark of lung cancer, especially high-grade and metastatic cancer. In vitro studies in H1299 cells confirmed that low miR-214 expression is associated with enhanced proliferation and migratory abilities. Similarly, CPD overexpression coincides with high-grade lung cancer and the CPD overexpression could reverse the inhibitory effects of miR-214. miR-214 is a tumor suppressor in lung cancer. miR-214 inhibits lung cancer progression by targeting CPD. The miR-214-CPD axis may be a therapeutic axis for lung cancer patients.
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Unique microRNA molecular profiles in lung cancer diagnosis and prognosis
Nozomu Yanaihara, Natasha J. Caplen, Elise D. Bowman et al. · Cancer Cell · 2006 · 3K citations · Full text
Osteoclast-derived exosomal miR-214-3p inhibits osteoblastic bone formation
Defang Li, Jin Liu, Baosheng Guo et al. · Nature Communications · 2016 · 588 citations · Full text