Abstract

BackgroundSignificant evidence has shown that the miRNA pathway is an important component in the downstream signaling cascades of TGF-β1 pathway. Our previous study has indicated that miR-335-5p expression was significantly down-regulated and acted as a vital player in the metastasis of non-small cell lung cancer (NSCLC), however the underlying mechanism remained unclear.MethodsThe differential expression level of miR-335-5p and ROCK1 were determined by qRT-PCR and IHC analysis in human tissue samples with or without lymph node metastasis. Transwell assay was conducted to determine cell ability of migration and invasion. SiRNA interference, microRNA transfection and western blot analysis were utilized to clarify the underlying regulatory mechanism.ResultsWe showed that down-regulated expression of miR-335-5p and up-regulated expression of ROCK1 in NSCLC tissues were associated with lymph node metastasis. Over-expresion of miR-335-5p significantly inhibited TGF-β1-mediated NSCLC migration and invasion. Furthermore, luciferase reporter assays proved that miR-335-5p can bind to 3′-UTR of ROCK1 directly. Moreover, we confirmed that siRNA-mediated silencing of ROCK1 significantly diminished TGF-β1-mediated EMT and migratory and invasive capabilities of A549 and SPC-A1 cells.ConclusionThis is the first time to report that miR-335-5p regulates ROCK1 and impairs its functions, thereby playing a key role in TGF-β1-induced EMT and cell migration and invasion in NSCLC.

Highlights

  • Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related death worldwide [1, 2]

  • Data from our analysis indicated that miR-335-5p can suppress transforming growth factor β1 (TGF-β1)-induced epithelial-mesenchymal transition (EMT) by binding to Rho associated protein kinase 1 (ROCK1) directly in non-small cell lung cancer (NSCLC)

  • MiR-335-5p over-expression inhibits the migratory ability of NSCLC cells To evaluate the function of miR-335-5p in NSCLC, we first over-expressed miR-335-5p and assessed the possible effects of miR-335-5p on cell migration

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Summary

Introduction

Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related death worldwide [1, 2]. MicroRNAs (miRNAs) belong to small noncoding RNAs and the roles they play in tumor development are mediated by downstream signaling networks which can further regulate multiple cellular functions like proliferation and migration [5,6,7,8]. Comprehensive expression analysis has shown that multiple miRNAs contributed to the development of lung cancer [9, 10]. MiR-335-5p is mainly reported to function as a tumor suppressor of migration and invasion. Our previous study has indicated that miR-335-5p expression was significantly down-regulated and acted as a vital player in the metastasis of non-small cell lung cancer (NSCLC), the underlying mechanism remained unclear

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