RhoA inhibits apoptosis and increases proliferation of cultured SPCA1 lung cancer cells

Introduction

Medical interventions, including surgical resection, radiotherapy and chemotherapy, have provided therapeutic benefits for various lung cancer patients. However, tumor recurrence may occur due to the development of multidrug resistance (1). Therefore, identification of the molecular pathways involved in the proliferation and apoptosis of lung cancer cells is of primary concern, as this may facilitate the development of inhibitors of these signaling pathways (2).

Cell migration, cell-to-cell adhesion, actomyosin contraction, mitosis and cytokinesis involve the Ras homolog (Rho)/Rho-kinase signaling pathway (3). In addition, numerous studies have demonstrated that the Rho/Rho-kinase pathway is prominently involved in cancer invasion, growth and metastasis, and Rho guanosine triphosphate hydrolases (GTPase) are involved in Ras-mediated oncogenic transformation (4,5). Numerous cancers exhibit overexpression of members of the small GTPase Rho family, including Rho family members A, C, H, Ras-related C3 botulinum toxin substrate 1 and cell division control protein 42 (6–8). Therefore, the aim of the present study was to investigate whether the Rho/Rho-kinase signaling pathway may be involved in the proliferation and apoptosis of lung cancer cells (9,10). A previous study demonstrated that the Rho-kinase inhibitor Fasudil, inhibited the Rho/Rho-kinase pathway, which subsequently inhibited the proliferation, invasion, adhesion and migration of lung cancer cells and induced apoptosis (11,12).

The aim of the present study was to examine the role of RhoA in the proliferation and apoptosis of lung cancer cells. Loss of RhoA expression was achieved using RNA interference (RNAi) in SPCA1 lung carcinoma cells, and the consequences on cell proliferation and apoptosis were subsequently analyzed. The use of RNAi involves double-stranded RNA (dsRNA) sequences that are homologous to the target gene, which results in sequence-specific, post-transcriptional gene silencing (13). Stable SPCA1 cell lines with silenced RhoA expression were isolated following Geneticin (G418) screening. The authors then tested the hypothesis that RhoA affects lung cancer proliferation and apoptosis. A secondary aim was to identify the underlying molecular pathways involved in these processes.

Materials and methods

Cell culture

SPCA1 human lung carcinoma cells were purchased from the Cell Bank of Type Culture Collection of The Chinese Academy of Sciences (Shanghai, China). Cells were cultured in RPMI-1640 medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 15% heat-inactivated fetal bovine serum (Thermo Fisher Scientific, Inc.), 100 mg/ml streptomycin and 100 U/ml penicillin (Beyotime Institute of Biotechnology, Haimen, China) at 37°C in a humidified atmosphere with 5% CO2.

Vector synthesis

The authors used a BLAST program to design oligonucleotides based on a RhoA cDNA sequence in Genbank, which were produced by Takara Biotechnology Co., Ltd. (Dalian, China). The sequences were as follows: Small interfering (si) RhoA-B, ′5-GCTAATACTAGCGGACTCCGATCTGCCGGAGTCCGCTAGTATTAGAAAAAACAGCTGTTCGA-5′, and siRhoA-, 5′-GATCCGATTATGATCGCCTGAGGCTCAAGACGGCCTCAGGCGATCATAATCTTTTTGTCGACA-3′. The oligonucleotides and pRNAT-U6.1/Neo-SiRNA vector (Takara Biotechnology Co., Ltd.) were digested by BamHI and HindIII (New England BioLabs, Inc., Ipswich, MA, USA) overnight at 37°C, then connected by T4 ligase (Thermo Fisher Scientific, Inc.) for 1 h at room temperature. Following this, the recombinant plasmid was transfected into DH5α (Takara Biotechnology Co., Ltd.) and screened overnight at 37°C. The recombinant vector was selected from single colonies and amplified, finally confirmed by electrophoresis and DNA sequencing (14).

Determination of G418 screening concentration

SPCA1 cells during the logarithmic phase of growth were digested with 0.25% pancreatin (Hyclone; GE Healthcare Life Sciences, Logan, UT, USA) and seeded in 96-well plates. The following day, 11 different concentrations of G418 (Gibco; Thermo Fisher Scientific, Inc.; 0–1,000 µg/ml in 100 µg/ml increments) were added to the wells. Six replicate wells were used for each concentration. In order to avoid the edge effect, the outer wells of the culture plate were not used. Cells were observed for 1 week, with the medium refreshed once in the middle of the week. Cells exhibited various rates of survival for concentrations of G418 between 0 and 400 µg/ml, however a G418 concentration of between 500 and 1000 µg/ml resulted in comprehensive cell death by day 7. A concentration of 500 µg/ml G418 was therefore selected as the screening concentration, and 200 µg/ml G418 as the maintenance concentration.

RhoA siRNA transfection and establishment of stable cell lines

SPCA1 cells in the logarithmic phase of growth, and at passage number <10, were transfected with RhoA siRNA. Each transfection included a control group (transfected with empty vectors). SPCA1 cells (2×105 cells/well) were seeded in 6-well plates. Following incubation for 24 h, cells were transfected with RhoA siRNA in serum-free medium using Lipofectamine® 2000 (Invitrogen; Thermo Fisher Scientific, Inc.) in accordance with the manufacturer's protocol. A mixture containing 4 µg vector and 10 µl Lipofectamine 2000™ was incubated for 20 min at room temperature. SPCA1 cells were then washed and incubated with the vector-Lipofectamine mixture for 24 h in a CO2 incubator at 37°C. A total of 500 and 200 µg/ml G418 was then added to wells for three weeks in order to screen for and maintain the growth of stable RhoA siRNA-transfected cells, respectively. The recombinant plasmid RhoA-pRNAT-U6.1/Neo-SiRNA were selected from single colonies and amplified, so the SPCA1 cell lines expressing RhoA-pRNAT-U6.1/Neo-SiRNA could emit GFP continuously. Transfection was visualized using fluorescence microscopy (DFC365FX; Leica Microsystems GmbH, Wetzlar, Germany).

Western blot analysis

Stable RhoA siRNA-transfected cells and controls were subject to western blot analysis. To do this, cells were first washed three times with ice-cold PBS, before they were lysed in lysis buffer for 30 min in an ice-bath. Following electrophoresis (30 µg/well) on 10% SDS-PAGE gels, separated protein samples were transferred to a nitrocellulose membrane. The membrane was then blocked in 5% non-fat dry milk in TBS with 0.05% Tween-20 (TBST) for 1 h at room temperature, to prevent nonspecific antibody binding. Following incubation with rabbit anti-RhoA antibody (dilution, 1:250; Jingmei Biotech Co., Ltd., Beijing, China) at 4°C overnight, the membrane was incubated with goat anti-rabbit antibody (dilution, 1:500; Jingmei Biotech Co., Ltd.). An antibody to β-actin (Sigma-Aldrich; Merck Millipore, Darmstadt, Germany) served as a loading control. For the detection of caspase-3 and signal transducer and activator of transcription (STAT) 3, cell lysates (40 µg each of protein) from stable RhoA siRNA-transfected and control cells were added to 2X Laemmli sample buffer (Hyclone; GE Healthcare Life Sciences), boiled for 5 min and electrophoresed under the aforementioned conditions with 10% SDS-PAGE gels. Proteins were transferred to polyvinylidene difluoride membranes (Bio-Rad Laboratories, Inc., Hercules, CA, USA), rinsed with TBST (pH 7.5), and blocked in 5% non-fat dry milk in TBST overnight at 4°C. Membranes were incubated in polyclonal anti-STAT3, anti-caspase or anti-phosphorylated (phospho)-STAT3 (Tyr-705) primary antibodies for 3 h. Following rinsing in TBST, the membrane was incubated with horseradish peroxidase-conjugated goat anti-rabbit antibody (EMD Millipore, Billerica, MA, USA) for 50 min. Protein bands were detected by enhanced chemiluminescence (Pierce; Thermo Fisher Scientific, Inc.). Densitometry was used to semi-quantify band intensities.

Cell proliferation assay

An MTS tetrazolium assay was used to measure cell proliferation, as previously described (15). Briefly, RhoA siRNA-transfected cells or controls were seeded into 96-well plates (1,000 cells/well) in 100 µl/well of RPMI 1640 medium. Five replicates for each experimental group and time points (0, 24, 48 and 96 h) were used. Following 24 h, 20 µl CellTiter 96 AQueous One Solution (Promega Corporation, Madison, WI, USA) was added to each well, and cells were incubated at 37°C for a further 4 h. Absorbance was measured at a wavelength of 490 nm each day for 7 days.

Fluorescence-activated cell sorting (FACS) analysis

Cell apoptosis in treated and untreated cells was measured by FACS or flow cytometry analysis, using the methods described previously (16). The FITC-Annexin V Apoptosis Detection kit (BD Pharmingen, San Diego, CA, USA) was used according to the manufacturer's protocol. Briefly, fluorescein isothiocyanate (FITC)-Annexin V and propidium iodide (PI) were used to stain siRNA RhoA-transfected and control cells for 5 min at room temperature. Annexin V−PI− (viable cells) and Annexin V+ (apoptotic) cells were evaluated by flow cytometry. A BD FACSCalibur flow cytometer (BD Biosciences, Franklin lakes, NJ, USA) was used to collect data that was then analyzed using BD CellQuest software (BD Biosciences).

Statistical analysis

Data are expressed as the mean ± standard error. Variables were compared using the Student's t-test, the χ2 test and analysis of variance or Fisher's exact test. Data were analyzed using SPSS software (version 17.0; SPSS, Inc., Chicago, IL, USA). P<0.05 was considered to indicate a statistically significant difference.

Results

Successful generation of stable RhoA siRNA-transfected SPCA1 cell lines and western blot analysis of RhoA expression

In order to generate a RhoA-pRNAT-U6.1/Neo-SiRNA vector, oligonucleotide dsRNAs were ligated with pSUPER following annealing. The sequence of synthesized siRNA oligos and insert sequences were indistinguishable (Fig. 1A). Stable RhoA siRNA-transfected SPCA1 lung cancer cell lines were then generated (Fig. 1B). RhoA protein expression was analyzed by western blotting using an anti-RhoA antibody. As shown in Fig. 1C, a marked reduction in RhoA protein expression in RhoA siRNA-transfected cells was observed when compared with the control cells (Fig. 1C).

Figure 1. Generation of stable RhoA siRNA-transfected SPCA1 lung cancer cells and western blot analysis of RhoA protein expression. (A) Sequence analysis of recombinant plasmids and synthesized siRNA oligonucleotides. (B) RhoA siRNA-transfected SPCA1 cell lines under a fluorescence microscope (magnification, ×50). (C) Western blot analysis of RhoA protein expression. Lane 1, control cells; lane 2, RhoA siRNA-transfected cells. Rho, Ras homolog family member A; siRNA, small interfering RNA.

RhoA silencing decreases proliferation of cultured SPCA1 lung cancer cells

The proliferation rate of stable RhoA siRNA-transfected cells was significantly lower when compared with the control cells every day for 7 days (P<0.01; Fig. 2), as determined using the MTS assay. These results suggested that silencing of RhoA expression significantly decreased SPCA1 cell proliferation.

Figure 2. Effects of RhoA siRNA on the proliferation of cultured SPCA1 lung cancer cells. The proliferation of RhoA siRNA-transfected SPCA1 lung cancer cells was measured over the course of seven consecutive days using an MTS assay. Following RhoA knockdown, a significant decrease in the proliferation of SPCA1 cells was observed when compared with the control cells. **P<0.01 vs. control. RhoA, Ras homolog family member A; siRNA, small interfering RNA.

RhoA silencing increases apoptosis of cultured SPCA1 lung cancer cells

Flow cytometry was used to assess the level of apoptosis in RhoA siRNA-transfected SPCA1 cells. As shown in Fig. 3, stable RhoA siRNA-transfected cells exhibited a significant increase in the rate of apoptosis when compared with the control cells (P<0.01). These results suggested that RhoA silencing was associated with a marked increase in the level of apoptosis in SPCA1 cells.

Figure 3. Level of apoptosis in cultured RhoA siRNA-transfected SPCA1 lung cancer cells. (A and B) RhoA siRNA-transfected cells and controls were collected and stained with annexin V (apoptosis stain) and PI (nuclear stain), and analyzed by flow cytometry. (C) The results from one of three independent assays are presented. The level of apoptosis in RhoA siRNA-transfected cells was significantly greater when compared with the control cells. **P<0.01 vs. control. RhoA, Ras homolog family member A; siRNA, small interfering RNA; UR, upper right; LR, lower right; PI, propidium iodide; FITC, fluorescein isothiocyanate.

RhoA silencing induces activation of caspase-3 in cultured SPCA1 lung cancer cells

As shown in Fig. 4, a significant increase in caspase-3 expression in stable RhoA siRNA-transfected cells was observed when compared with the control cells, as determined by western blotting (P<0.01). By contrast, caspase-9 activation remained unaffected between the two groups (Fig. 4). These results suggest that RhoA silencing may activate caspase-3.

Figure 4. Activation of caspase-3 and caspase-9. (A) Western blot analysis of casp-3, casp-9 and β-actin protein expression in RhoA siRNA-transfected SPCA1 cells and untreated controls using anti-casp-3, anti-casp-9 and β-actin antibodies. β-actin was used as a loading control. (B) A significant increase in the active casp-3 form was observed in RhoA siRNA-transfected cells when compared with the control cells. By contrast, RhoA knockdown did not significantly alter casp-9 activation. **P<0.01 vs. control. RhoA, Ras homolog family member A; siRNA, small interfering RNA; casp-3, caspase-3; casp-9, caspase-9.

RhoA silencing downregulates STAT3 phosphorylation in cultured SPCA1 lung cancer cells

The level of phopho-STAT3 were decreased by 33.1% in stable RhoA siRNA-transfected cells when compared with control cells (P<0.01; Fig. 5) as determined by western blotting analysis. By contrast, no significant difference in STAT3 protein expression levels between the groups was observed (Fig. 5). Therefore, RhoA silencing may decrease the expression levels of phospho-STAT3 in SPCA1 cells.

Figure 5. Protein expression levels of STAT3 and p-STAT3 in RhoA siRNA-transfected SPCA1 cells. (A) STAT3 and p-STAT3 (Tyr 705) protein expression levels were measured by western blotting and subsequent densitometry analysis (mean ± standard error; n=3). (B) Quantification of STAT3 and p-STAT3 protein expression levels. Following RhoA knockdown, the level of p-STAT3 decreased by 31.5% in RhoA siRNA-transfected cells, whereas RhoA siRNA did not significantly affect STAT3 protein levels. **P<0.01 vs. control. STAT3, signal transducer and activator of transcription 3; p-STAT3, phosphorylated-STAT3; RhoA, Ras homolog family member A; siRNA, small interfering RNA.

Discussion

The deregulation of cell proliferation and apoptosis pathways is a prerequisite for the development of lung cancer (17). At present, current cancer therapies consist of agents that target signaling pathways involved in cell proliferation, which result in cell death, for example, gemcitabine hydrochloride (18). However, further investigation into the mechanisms involved in cancer development is required in order to develop novel and improved anti-cancer therapies.

Activation of the Rho/Rho kinase pathway is important for cell migration, cell-to-cell adhesion, invasion and mitosis (19,20), and may additionally be predominant in cancer growth and invasion (21). In non-small cell lung cancers, inhibition of the Rho/Rho-kinase pathway impedes tumour migration and invasion (10,11). The aim of the present study was to assess the consequences of RhoA silencing in lung cancer cells at various stages of carcinogenesis, including proliferation and apoptosis.

RNAi is considered to be a precise method of gene silencing, which can involve the use of siRNA (22). This method was used to construct an RhoA siRNA expression vector in the present study, which was subsequently transfected into SPCA1 lung cancer cells. A stable RhoA siRNA-transfected SPCA1 cell line was successfully established and it was verified that RhoA siRNA reduced RhoA expression in SPCA1 lung cancer cells. It was demonstrated that knockdown of RhoA resulted in inhibition of lung cancer cell viability. Using flow cytometry analysis, it was subsequently demonstrated that a knockdown of RhoA significantly induced apoptosis in SPCA1 cells.

Western blot analysis was then performed in order to examine the activation of caspases as a possible mechanism underlying the increased levels of apoptosis observed in SPCA1 cells in response to RhoA knockdown. A significant increase in caspase-3, but not caspase-9 expression, was observed in RhoA siRNA-transfected SPCA1 cells. This was consistent with the results obtained from FACS analysis. Therefore, RhoA knockdown induced strong activation of caspase-3 in SPCA1 cells, which suggests that caspase-dependent apoptosis may have contributed to the RhoA knockdown-mediated, anti-proliferative effects observed in SPCA1 cells.

Cellular transformation in response to constitutive activation of STAT3 is frequently observed in numerous human cancer cells (23). In the present study, western blotting was used to determine whether the observed RhoA siRNA-mediated inhibition of SPCA1 cell proliferation was the result of STAT3 inactivation, by determining the phosphorylation status of STAT3. RhoA knockdown resulted in a significant decrease in phospho-STAT3 (Tyr-705) levels, however, no effect on total STAT3 protein levels was observed. The results suggested that RhoA knockdown induced cell growth inhibition and apoptotic cell death in SPCA1 cells, which may be associated with STAT3 inactivation.

In conclusion, the results of the present study suggest that RhoA may be important for lung cancer cell proliferation and apoptosis. Alterations in caspase-3 and phospho-STAT3 levels and activation may be the underlying molecular mechanisms associated with the effect of RhoA on SPCA1 cell proliferation and apoptosis. These results provide an improved understanding of the cellular pathways involved in human lung cancer, and may facilitate the development of novel therapies to treat patients with this disease.

Acknowledgements

The present study was supported by The Specialized Research Fund for the Doctoral Program of Higher Education of China (grant no. 20122104120015).

References