51. miR-370 targeted FoxM1 functions as a tumor suppressor in laryngeal squamous cell carcinoma (LSCC)
- Author
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Li Wenming, Wu Yungang, Li Xiaoyu, Taizhong Pang, and Xinliang Pan
- Subjects
Pathology ,medicine.medical_specialty ,Molecular Sequence Data ,Cell Culture Techniques ,Down-Regulation ,Biology ,Transfection ,law.invention ,Pathogenesis ,Downregulation and upregulation ,Genes, Reporter ,law ,Cell Line, Tumor ,microRNA ,medicine ,Humans ,Genes, Tumor Suppressor ,Laryngeal Neoplasms ,Cell Proliferation ,Luciferases, Renilla ,Pharmacology ,Binding Sites ,Base Sequence ,Cell growth ,Forkhead Box Protein M1 ,Forkhead Transcription Factors ,General Medicine ,Laryngeal squamous cell carcinoma ,Up-Regulation ,MicroRNAs ,Carcinoma, Squamous Cell ,FOXM1 ,Cancer research ,Suppressor ,Function (biology) ,Plasmids - Abstract
microRNAs, a family of small non-coding RNAs, involve in the pathogenesis of several types of cancers, including laryngeal squamous cell carcinoma (LSCC). MiR-370 is frequently aberrant expressed in various types of human cancer including LSCC. However, the role for miR-370 in LSCC remains elusive. Here, we demonstrate that miR-370 was down-regulated in human LSCC tissues. Furthermore, there was an inverse relationship between Forkhead Box ml (FoxM1), which was up-regulated and miR-370 expression in LSCC tissues. FoxM1 was subsequently predicted by bioinformatics and verified to be a target of miR-370 by Luciferase reporter assay. Restored expression of miR-370 in Hep2 cells significantly inhibited cell proliferation. In conclusion, our results suggest that miR-370 may function as a tumor suppressor in LSCC through downregulation of FoxM1, suggesting that miR-370 could serve as a novel potential maker for LSCC therapy.
- Published
- 2014
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