TRIzol reagent, fetal bovine serum (FBS), Lipofectamine 2000, SYBR Green qPCR Mix and the miRNA Reverse Transcription kit were purchased from Life Technologies (Thermo Fisher Scientific, Inc., Waltham, MA, USA). The miRNA Q-PCR Detection kit was purchased from GeneCopoeia (Rockville, MD, USA). The QuikChange Site-Directed Mutagenesis kit was purchased from Stratagene (Agilent Technologies, Inc., Santa Clara, CA, USA). The PsiCHECK™-2 vector was purchased from Promega Corporation (Madison, WI, USA). Mouse anti-FSCN1 and mouse anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) primary antibodies, and the rabbit anti-mouse secondary antibody were purchased from Abcam (Cambridge, MA, USA). The enhanced chemiluminescence (ECL) kit was purchased from Pierce Biotechnology, Inc. (Rockford, IL, USA).

Human embryonic kidney 293T (HEK 293T) cells, five human NSCLC cell lines (A549, L78, H1229, H358 and H1650) and a normal human lung epithelial cell line BEAS-2B were purchased from the Cell Bank of Central South University (Changsha, China). All cells were cultured in Dulbecco's modified Eagle's medium (DMEM; Thermo Fisher Scientific, Inc.) supplemented with 10% FBS at 37°C with 5% CO₂.

Total RNA was extracted using TRIzol reagent. For the detection of miRs, the miRNA Reverse Transcription kit was used to convert RNA into 1 µg cDNA, according to the manufacturer's instructions. RT-qPCR was then performed using a the miRNA Q-PCR Detection kit on the ABI 7500 thermocycler (Applied Biosystems; Thermo Fisher Scientific, Inc.). The U6 gene was used as an internal reference gene for miRNA. For mRNA detection, RT-qPCR analysis was performed using SYBR Green qPCR Mix and specific primers synthesized by Sangon Biotech Co., Ltd. (Shanghai, China). The specific primer pairs used were as follows: FSCN1, sense 5′-CACAGGCAAATACTGGACGGT-3′ and antisense 5′-CCACCTTGTTATAGTCGCAGAAC-3′; and GAPDH, (internal reference gene for mRNA) sense 5′-ACAACTTTGGTATCGTGGAAGG-3′ and antisense 5′-GCCATCACGCCACAGTTTC-3′. The RT-qPCR cycling conditions were as follows: 95°C for 10 min, 40 cycles of denaturation at 95°C for 15 sec and annealing/elongation at 60°C for 60 sec. The relative expression was analyzed using the 2^−ΔΔCq method (11).

Cells were solubilized in cold radioimmunoprecipitation assay lysis buffer (Beyotime Institute of Biotechnology, Haimen, China). Subsequently, the proteins (20 µg per lane) were separated with 10% sodium dodecyl sulfate-polyacrylimide gel electrophoresis (Beyotime Institute of Biotechnology), then transferred from the gel to a nitrocellulose membrane (Thermo Fisher Scientific, Inc.), which was then incubated with Tris-buffered saline with Tween 20 (Beyotime Institute of Biotechnology) containing 5% milk at room temperature for 3 h. The membrane was then incubated with monoclonal mouse anti-FSCN1 (1:100; ab49815) and monoclonal mouse anti-GAPDH (1:50; ab8245) primary antibodies at room temperature for 3 h, and then with the monoclonal rabbit anti-mouse secondary antibody (1:10,000; ab190475) at room temperature for 40 min. Subsequently, immune complexes were detected using the ECL kit. The membrane was scanned for the relative value of protein expression using the Tanon 6600 Luminescent Imaging Workstation (Tanon Science & Technology Co., Ltd., Shanghai, China), measuring the grayscale with Image-Pro Plus software, version 6.0 (Media Cybernetics, Inc., Rockville, MD, USA). The relative expression levels of the proteins were presented as the density ratio vs. GAPDH.

The plasmid of FSCN1, scramble miRNA mimics, miR-200b mimics and the miR-200b inhibitor were generated by Shanghai GenePharma Co., Ltd. (Shanghai, China). Lipofectamine 2000 was used to perform transfection according to the manufacturer's instructions. The plasmid, miRNA mimics and Lipofectamine 2000 were diluted with DMEM, respectively, and were then incubated for 20 min at room temperature and added into the cell suspension. The cells were then incubated at 37°C with 5% CO₂ for 6 h. Subsequently, the medium in each well was replaced by DMEM supplemented with 10% FBS, and cultured for 24 h prior to experimentation.

A QuikChange Site-Directed Mutagenesis kit was used to generate a mutant type 3′-UTR of FSCN1, according to the manufacturer's instructions. The wild type (WT) or mutant type (MUT) of FSCN1 3′-UTR were inserted into the psiCHECK™2 vector. Subsequent to culture of HEK 293T cells to approximately 70% confluence, the cells were transfected with the psiCHECK™2-FSCN1-3′-UTR or psiCHECK™2-MUT FSCN1-3′-UTR vector, with or without 100 nM miR-200b mimics. Subsequent to transfection for 48 h, the luciferase activities were determined using an LD400 Luminometer (Beckman Coulter, Inc., Brea, CA, USA). Renilla luciferase activity was normalized to firefly luciferase activity.

The invasive ability of H1229 cells was determined using 24-well Transwell chambers (BD Biosciences, Franklin Lakes, NJ, USA), with an added layer of Matrigel. For each group, the cell suspension was added into the upper chamber, and DMEM containing 10% FBS was added into the lower chamber. Subsequent to incubation for 24 h, non-invading H1229 cells in addition to the matrix gel on the interior of the inserts was removed using a cotton-tipped swab. Invasive H1229 cells on the lower surface of the membrane were stained with 0.1% gentian violet (Beyotime Institute of Biotechnology), and then rinsed with water, air-dried, then observed under a microscope (VM4800M; Nikon Corporation, Tokyo, Japan).

The wound healing assay was performed to evaluate cell migration. In brief, H1229 cells were cultured to full confluence. Wounds of approximately 1 mm width were created using a plastic scriber. Subsequently, the cells were washed with phosphate-buffered saline (Thermo Fisher Scientific, Inc.) and cultured in DMEM containing 10% FBS. Subsequent to culture at 37°C with 5% CO₂ for either 0 h or 48 h, the cells were fixed and observed under a microscope.

The putative target genes of miR-200b were then identified by performing bioinformatics analysis using TargetScan software (http://www.targetscan.org/), according to the manufacturer's instructions. 'Human' was selected as the species, and 'miR-200b' was entered as the search term.

The results are expressed as the mean ± standard deviation of a minimum of three independent experiments. Statistical analysis of differences was performed by one-way analysis of variance. Statistical analysis was performed using SPSS software, version 17.0 (SPSS, Inc., Chicago, IL, USA). P<0.05 was considered to indicate a statistically significantly difference.

RT-qPCR analysis was conducted in order to examine the expression levels of miR-200b in the A549, L78, H1229, H358 and H1650 human NSCLC cell lines, in addition to a normal human lung epithelial cell line BEAS-2B. As presented in Fig. 1, miR-200b was significantly downregulated in all NSCLC cell lines apart from H358, when compared with the BEAS-2B cells, thus suggesting that deregulation of miR-200b may serve a role in the development and progression of NSCLC. In addition, as H1229 cells were observed to exhibit the greatest reduction in miR-200b expression, they were selected for use in the subsequent experiments.

The role of miR-200b was then investigated in the regulation of NSCLC cell migration and invasion. H1229 cells were transfected with miR-200b mimics or scramble miR mimics as a negative control. As presented in Fig. 2A, transfection with miR-200b mimics significantly upregulated the expression levels of miR-200b in H1229 cells compared with the control group. A wound healing assay and Transwell assay were then conducted in order to examine the cell migration and invasion in each group. As presented in Fig. 2B and C, overexpression of miR-200b significantly reduced the migratory and invasive capacities of H1229 cells compared with the control group, suggesting that miR-200b exhibits suppressive effects on NSCLC cell migration and invasion.

The putative target genes of miR-200b were then conducted by performing bioinformatics analysis. This identified that the putative seed sequences for miR-200b at the 3′UTR of FSCN1 were conserved. To clarify whether FSCN1 is a target gene of miR-200b, the WT and MUT of FSCN1 3′-UTR were inserted into the psiCHECK™2 vector, generating Luc-FSCN1 3′UTR or Luc-MUT FSCN1 3′UTR, respectively (Fig. 3A). Subsequently, HEK 293T cells were transfected with Luc-FSCN1 3′UTR or Luc-MUT FSCN1 3′UTR, with or without 100 nM miR-200b mimics. Luciferase reporter assay data indicated that the luciferase activity was reduced in HEK 293T cells co-transfected with Luc-FSCN1 3′UTR and miR-200b mimics, however was unchanged in the remaining groups (Fig. 3B), indicating miR-200b is able to directly bind to the 3′UTR of FSCN1.

It was further investigated whether the expression of FSCN1 was negatively mediated by miR-200b in H1229 cells. Subsequent to transfection with miR-200b mimics or the inhibitor, the miR-200b levels were examined in NSCLC H1229 cells. As presented in Fig. 4A, transfection with miR-200b mimics upregulated the miR-200b level, while transfection with miR-200b inhibitor resulted in reduced miR-200b expression in H1229 cells. The protein levels of FSCN1 were then determined in each group, and it was identified that overexpression of miR-200b resulted in a reduced protein level of FSCN1, while inhibition of miR-200b expression upregulated FSCN1 protein expression in H1229 cells (Fig. 4B). Therefore, it was demonstrated that the protein level of FSCN1 is negatively mediated by miR-200b in H1229 NSCLC cells.

As it has been demonstrated that FSCN1 is able to enhance NSCLC cell migration and invasion (11), it was hypothesized that the suppressive effects of miR-200b on H1229 cell migration and invasion may be via inhibition of FSCN1 expression. To verify this hypothesis, H1229 cells overexpressing miR-200b were further transfected with the FSCN1 plasmid in order to restore FSCN1 expression. As presented in Fig. 5A, the protein levels of FSCN1 were significantly greater in H1229 cells co-transfected with miR-200b mimics and FSCN1 plasmid, when compared with that of H1229 cells transfected with miR-200b mimics. Further investigation indicated that transfection with the FSCN1 plasmid significantly reversed the suppressive effects of miR-200b overexpression on H1229 cell migration and invasion (Fig. 5B and C). Accordingly, it was suggested that FSCN1 is involved in miR-200b-mediated migration and invasion in H1229 cells.