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MiR-152 suppresses the proliferation and invasion of NSCLC cells by inhibiting FGF2
MiR-152 suppresses the proliferation and invasion of NSCLC cells by inhibiting FGF2
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MiR-152 suppresses the proliferation and invasion of NSCLC cells by inhibiting FGF2
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MiR-152 suppresses the proliferation and invasion of NSCLC cells by inhibiting FGF2
MiR-152 suppresses the proliferation and invasion of NSCLC cells by inhibiting FGF2
Journal Article

MiR-152 suppresses the proliferation and invasion of NSCLC cells by inhibiting FGF2

2014
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Overview
MicroRNAs (miRNAs) regulate the proliferation and metastasis of cancer cells. Here, we showed that miR-152 was downregulated in non-small-cell lung cancer (NSCLC) tissues and cell lines. Overexpression of miR-152 suppressed cell proliferation and colony formation and also limited migration and invasion. Fibroblast growth factor 2 (FGF2) was confirmed as a direct target of miR-152. FGF2 knockdown suppressed cell proliferation, colony formation, migration and invasion, whereas FGF2 overexpression partially reversed the suppressive effect of miR-152. Furthermore, the presence of miR-152 was inversely correlated with FGF2 in NSCLC tissues. Overall, this study demonstrated that miR-152 suppressed the proliferation and invasion of NSCLC cells by downregulating FGF2. These findings provide novel insights with potential therapeutic applications for the treatment of NSCLC. Cancer: Slowing the growth of lung cancer cells The growth and spread of lung cancer cells in tissue culture can be slowed by boosting levels of a specific microRNA. MicroRNAs are small non-coding RNAs, known to regulate gene expression and play a role in some cancers. Tumor cells from patients with non-small cell lung cancer (NSCLC) have lower levels of one particular microRNA, called miR-152, according to Zhenshun Cheng from China's WuHan University and colleagues. Increasing levels of the microRNA inhibited cancer cell growth and spread by targeting fibroblast growth factor 2, a protein that has previously been linked to cell division and blood vessel growth. NSCLC accounts for over 80% of all lung cancers and carries a dismal prognosis. Understanding exactly how miR-152 produces its effects will aid in the development of improved treatments and prognostic tools.

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