The TNF‐α‐induced expression of miR‐130b protects cervical cancer cells from the cytotoxicity of TNF‐α

Tumour necrosis factor alpha (TNF‐α) is a multifunctional cytokine and has the capacity both to promote cell growth and to kill tumour cells by inducing cell apoptosis. However, many tumour cells develop resistance to the toxic effects of TNF‐α. Thus, understanding the mechanism underlying the resistance of tumours to TNF‐α toxicity and finding ways to overcome this resistance are urgently needed. In this study, we discovered that two cervical cancer cell lines, Hela and Siha, showed null responses to TNF‐α cytotoxicity. However, in these cell lines, TNF‐α stimulation promoted the expression of miR‐130b and downregulated the expression of PTEN gene, which encodes a dual‐specificity phosphatase that acts as a tumour suppressor. Blockade of miR‐130b function or overexpression of PTEN gene sensitized cells to TNF‐α cytotoxicity. Regression analyses revealed that there were reverse relationships between the cellular levels of miR‐130b and PTEN mRNA in cervical cancer cells. Gain‐ and loss‐of‐function assays demonstrated that there were causal relationships between the increase in miR‐130b levels and the reduction in PTEN mRNA or PTEN protein levels. In silico analysis revealed that there were two miR‐130b target sites within the 3′UTR of PTEN mRNA and experimental evidences demonstrated that miR‐130b repressed the expression of PTEN gene by binding directly to the 3′UTR of PTEN mRNA. These data suggest miR‐130b expression as a target to be inhibited to make tumour cells more sensitive to the toxic impact of TNF‐α.

Tumour necrosis factor alpha (TNF-a) is a multifunctional cytokine and has the capacity both to promote cell growth and to kill tumour cells by inducing cell apoptosis. However, many tumour cells develop resistance to the toxic effects of TNF-a. Thus, understanding the mechanism underlying the resistance of tumours to TNF-a toxicity and finding ways to overcome this resistance are urgently needed. In this study, we discovered that two cervical cancer cell lines, Hela and Siha, showed null responses to TNF-a cytotoxicity. However, in these cell lines, TNF-a stimulation promoted the expression of miR-130b and downregulated the expression of PTEN gene, which encodes a dual-specificity phosphatase that acts as a tumour suppressor. Blockade of miR-130b function or overexpression of PTEN gene sensitized cells to TNF-a cytotoxicity. Regression analyses revealed that there were reverse relationships between the cellular levels of miR-130b and PTEN mRNA in cervical cancer cells. Gain-and loss-of-function assays demonstrated that there were causal relationships between the increase in miR-130b levels and the reduction in PTEN mRNA or PTEN protein levels. In silico analysis revealed that there were two miR-130b target sites within the 3 0 UTR of PTEN mRNA and experimental evidences demonstrated that miR-130b repressed the expression of PTEN gene by binding directly to the 3 0 UTR of PTEN mRNA. These data suggest miR-130b expression as a target to be inhibited to make tumour cells more sensitive to the toxic impact of TNF-a.
Tumour necrosis factor alpha (TNF-a) is a 26-kilodalton (kDa) type II transmembrane protein, which is arranged in a stable homotrimers. Its soluble homotrimeric cytokine is derived from the transmembrane form through proteolytic cleavage by the metalloprotease TNF-a converting enzyme [1]. In the case of cancer development, TNF-a is a double-edged sword. On the one hand, it could act as an endogenous tumour promoter based on its abilities to stimulate the growth, proliferation, invasion and metastasis of cells [2][3][4]. On the other hand, it performs as a cancer killer relying on its capacity of inducing cell apoptosis [5]. The property of TNF-a in promoting the death of cancer cell suggests TNF-a to be a potential cancer therapeutic drug. Unfortunately, the cytotoxic effect of TNF-a is cell line specific and only a proportion of tumour Abbreviations 2 0 OMe, 2 0 -O-methylation; cDNA, complementary DNA; DMSO, dimethyl sulfoxide; FITC, fluorescein isothiocyanate; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GFP, green fluorescent protein; miRNA, microRNA; NF-jB, nuclear factor kappa-light-chainenhancer of activated B cells; NS, nonsignificant; PI, propidium iodide; PTEN, phosphatase and tensin homolog deleted on chromosome ten; SE, standard error; TBST, Tris-buffered saline with Tween-20; TNF-a, tumour necrosis factor alpha; UTR, untranslated region. cell lines are sensitive to TNF-a cytotoxicity [6]. Therefore, understanding the mechanism underlying the resistance of tumour cells to TNF-a killing and finding available approaches to overcome the drug resistance are urgently required.
MicroRNA (miRNA) refer to a class of small noncoding RNA of approximately 20 nucleotides in length. They play important roles in gene regulations in animals' cells by base pairing with the UTR of their target genes [7,8]. It was previously recorded that the upregulated expression of miR-19a in colorectal cancer cell responded to TNF-a stimulation-mediated TNF-ainduced epithelial-to-mesenchymal transition of the tumour cell [9]. The expression of miR-146a induced by TNF-a-inhibited TNF-a-induced adipogenesis via targeting insulin receptor [10]. Wei R and his coworkers found that the downregulated expression of miR-23a caused by TNF-a stimulation led to an increase in endothelial cell apoptosis induced by TNF-a [11]. Suarez Y and his fellows discovered that TNF-a enhanced the expression of miR-31 and miR-17-3p but the upregulated miRNA could antagonized the increased expression of E-selectin and intercellular adhesion molecules-1 (ICAM-1) triggered by TNF-a [12]. These literatures illustrated that TNF-a-induced miRNA could provide positive or negative feedback controls of the impacts of TNF-a on cell phenotypes by modulating the expression of their specific targeted genes.
The biological functions of miR-130b in the development of tumours were inconsistent in different cell lines. On the one hand, miR-130b made a negative effect on the development of some tumours. It inhibited cell proliferation and invasion in pancreatic cancer cell through downregulating STAT3 expression and suppressed the migration and invasion of colorectal cancer cell by decreasing the expression of integrin b1 [13,14]. On the other hand, the miRNA affected the tumour progression in a positive manner in other specific cells. In oesophageal squamous cell carcinoma cell, it worked as an oncogenic role by inhibiting the expression of PTEN gene [15]. The upregulation of miR-130b expression contributed to the development of thyroid adenomas by targeting CCDC6 gene [16]. MiR-130b could promote cell migration and invasion by decreasing the PTEN gene expression through FAK and Akt phosphorylation in bladder cancer [17]. By inhibiting the expression of peroxisome proliferator-activated receptor-c, miR-130b could promote the proliferation and invasion of human glioma cell [18]. As far as we know, there is lack of the research on the role of miR-130b in the cervical cancer cell line. In this study, we found that the expression of miR-130b was promoted by TNF-a treatment in cervical cancer cell but the increased expression of miR-130b affected the TNF-a cytotoxicity in a negative way. We tried to gain insight to the mechanism underlying this phenomenon through our study and demonstrated that the inhibition of miR-130b function enhanced the TNF-ainduced cell death of cervical cancer cell.

Materials and methods
Cell culture and TNF-a treatment Hela and Siha cells were planted in RPMI1640 medium supplemented with 10% (vol/vol) fetal bovine serum and 1% penicillin-streptomycin (vol/vol) and cultured in a humidified atmosphere containing 5% CO 2 at 37°C. The cultured cell was treated with either vehicle control formed by phosphate-buffered saline with 1 mgÁmL À1 bovine serum albumins (Sigma, St. Louis, MO, USA) or TNF-a solution of wanted concentration which was prepared using commercial stock solution of TNF-a (Sigma) for the desired incubation time period.

RNA extraction
RNA was extracted from the cultured cell using RNA Isolation kit (Ambion, Inc, Austin, TX, USA). The quality assessment of isolated RNA was achieved through the analysis of integrity using gel electrophoresis and that of purity by calculating the ratio between RNA absorbance at 260 nm and its absorbance at 280 nm.

The construction of vectors
The complementary DNA (cDNA) derived from a part of PTEN mRNA was synthesized within a vial containing SpnRT as a specific primer and reverse transcriptase following the manufacturer's instruction (Takara, Minato-ku, Tokyo, Japan). The DNA fragment encompassing the coding region of PTEN gene and Kozak sequence ahead of the coding region was obtained and amplified through PCR using one pair of primers, ptnF1 and ptnR1, in addition to the other pair of primers, ptnF2 and ptnR2. The amplification products were digested using restriction enzyme (Thermo Scientific, Waltham, MA, USA), BamHI and EcoRI, and linked into the corresponding cleavage sites within pcDNA3.1 vectors to form pcDNA3.1::PTEN vectors using T4 DNA ligases (Thermo Scientific). A part of PTEN mRNA bearing predicted sites targeted by miR-130b was reverse transcribed using a specific primer, SputrRT. Then, the two DNA fragments which encoded the parts of UTR of PTEN mRNA containing predicted targeted sites were separately amplified using two pairs of primers, putrU1 and putrD1 or putrU2 and putrD2, and then cloned into pEGFP vectors downstream of GFP coding domains to construct fusion vectors, pEGFP::wt1-UTR and pEGFP::wt2-UTR. The sequence complementary to the seed region of miR-130b either in position 2654-2661 or 4495-4502 of the PTEN mRNA, TTGCACT, was mutated to the sequence, TAGGAGT, using two additional pairs of primers, pnmutU1 and pnmutD1 or pnmutU2 and pnmutD2, based on the site-directed mutagenesis, respectively. The constructed vector containing mutated points within position 2654-2661 of the PTEN mRNA was named as pGFP::mut1-UTR and the vector containing points within position 4495-4502 as pGFP::mut2-UTR. The DNA sequences of all the available primers were listed in Table 1.

Semiquantitative real-time PCR assays
The RNA reverse transcriptions were achieved using reverse transcriptase following the product's manual (Takara). Realtime PCR assays were performed using cDNA generated in the reverse transcription assays containing 50 ng of total RNA templates to quantify the relative levels of the miR-130b according to the method described in the previous literature [19] and in the assays containing 200 ng of total RNA templates to determine the relative contents of PTEN mRNA using the protocol from a qRT-PCR mRNA detection kit (Roche, Indianapolis, IN, USA). Amplifications and measurements of specific products were performed on a Roche Lightcycler 480 Detection System. U6 small RNA were employed as internal controls for miRNA templates normalization and b-actin mRNA for PTEN templates normalization. The relative expression levels of RNA molecules in either TNF-a-treated cells or vehicle-treated cells were calculated using 2 ÀDDCT method [20]. The sequences of the primers utilized in the reverse transcription or real-time PCR assays were listed in Table 2.

Transfection of cervical cancer cells
The transfection of tumour cell with exogenous nucleotides was accomplished using Xfect transfection reagent according to the guideline provided by the manufacturer (Takara). Briefly, the oligonucleotides including the miR-130b mimics, miR-130b inhibitors and their respective scrambled control oligonucleotides were utilized at final concentrations of 50 pmolÁmL À1 and the plasmids including pcDNA3.1, pEGFP, rTagRFP and their respective derived plasmids were used at final concentrations of 3 lgÁmL À1 in the transfection assays unless otherwise noted. The miR-130b mimics are short double-stranded RNA. Each molecule is constituted by one guide strand whose sequence is identical to the sequence of mature miR-130b and one passenger stand partially complementary to the mature miR-130b sequence. The sequence of the guide strand is 'CAGUG-CAAUGAUGAAAGGGCAU', and the sequence of the passenger strand is 'GCCCUUUCAUCAUUGCACU-GUU'. The miR-130b inhibitors are single-stranded RNA with 2 0 -O-Methyl (2 0 OMe) modifications. Their sequences are complementary to the mature miR-130b sequences and presented as 'AUGCCCUUUCAUCAUUGCACUG'.

MTT reduction assays
Cancer cells were seeded on a 96-well plate at a density of 7000 cells per well and incubated in the medium overnight.
The underlined words represented the sequences recognized by restriction enzymes.
The primer was used to synthesize PTEN cDNA in the reverse transcription assay. b The primer was used to synthesize b-actin cDNA in the reverse transcription assay. c The primer was used to synthesize miR-130b cDNA in the reverse transcription assay. d The primer was used to synthesize the cDNA of U6 small RNA in the reverse transcription assay. e The pair of primers was used to amplify PTEN cDNA in the real-time PCR assay. f The pair of primers was used to amplify b-actin cDNA in the real-time PCR assay. g The pair of primers was used to amplify miR-130b cDNA in the real-time PCR assay. h The pair of primers was used to amplify the cDNA of U6 small RNA in the real-time PCR assay.
On the next day, the mediums were removed and replaced by the mediums containing TNF-a at indicated concentrations. About 20 lL of MTT solution (5 mgÁmL À1 ) was added to the medium at desired time point after the treatment of cell with TNF-a, and then, cells were incubated at 37°C for additional 4 h. Another 100 lL of DMSO was supplied to each well to dissolve the purple formazan crystals after the removal of MTT solution, and the plate was shaken at room temperature over a time course of 20 min. The optical density was detected at 570 nm using an EnSpire TM Multilabel Reader (PerkinElmer, Wallac Oy, Turku, Finland). The viabilities of cells cultured in the medium free of TNF-a were used as controls and considered as 100% of viabilities. Each group was composed of three independent assays.

The measurements of cell apoptosis
The cervical cancer cells were labelled using Annexin-V apoptosis kit according to the manufacturer's instruction (BD BioSciences, San Jose, CA, USA). The percentages of the apoptotic cells were determined using BD FACSCalibur Flow Cytometry System (BD BioSciences).

Western blot assays
The lysis of cervical cancer cell was achieved in RIPA buffer (Solarbio Science, Beijing, China) following the instruction provided by the manufacturer. The protein concentrations in the extracts were determined using BCA Protein Assay Kit (Takara). The extracts containing 30 lg of total proteins were mixed with commercial 59 protein loading buffer (Bosterbio, Pleasanton, CA, USA) and then subjected to 10% SDS/PAGE. After the proteins electroblotted to PVDF membrane (Bosterbio), the membrane was blocked with 5% nonfat milk in Tris-buffered saline with Tween-20 (TBST) buffer. The membrane was then incubated with mouse anti-PTEN or anti-GAPDH antibody (1 : 200 dilution; Bosterbio) at 4°C overnight. The membrane which was bound by anti-PTEN or anti-GAPDH antibody was washed three times with TBST buffer and then incubated with horseradish peroxidaseconjugated rabbit anti-mouse IgM (1 : 2000 dilution; Bosterbio) for 2 h. After that, the membrane was washed three times with TBST buffer once again. The protein contents were shown using an enhanced chemiluminescence detection kit (Bosterbio) and analysed using AL-PHAVIEW SA software (ProteinSimple, Santa Clara, CA, USA). The band intensities of GADPH proteins were utilized as internal controls for the normalization of PTEN protein levels.

Statistic analysis
All data were analysed using GRAPHPAD PRISM 5.0 software (GraphPad Software Inc, San Diego, CA, USA). The numerical data were calculated and described as means AE SEM. To determine the relative expression level of target gene, the mean value of the data obtained in control group was defined as 1 or 100%. Student's two-tailed unpaired t-tests were used for statistical evaluations of the data. The regression analysis was used to determine the relationship between two parameter sets. P values < 0.05 were considered to be significant.

Cervical cancer cells developed resistance to cytotoxicity mediated by TNF-a
To know the effects of TNF-a on the viabilities of cervical cancer cells, Hela and Siha cells were incubated with TNF-a at various concentrations and their viabilities were determined by MTT assays. As shown in Fig. 1A, there was no significant alteration among the viabilities of either Hela or Siha cells over 48-h incubation time periods. Additionally, it is well known that TNF-a shows its cytotoxicity by inducing apoptosis in a variety of cell types. To examine the impacts of TNF-a on the apoptosis rates of Hela and Siha cells, the target cells were cultured in the medium containing TNF-a at desired concentrations for 48-h time periods. As expected, there was no obvious change among the apoptosis rates of target cells after exposure to TNF-a (Fig. 1B). The TNF-a-induced expression of miR-130b protected cervical cancer cell from toxic activity of TNF-a The TNF-a-induced expressions of miR-130b have been described in both adipocyte and bladder carcinoma cell lines [21,22]. Through the analyses on the data from semiquantitative real-time RT-PCR assays, we found that the increment in the expression level of miR-130b was in correlation with the elevation in the concentration of TNF-a utilized to treat cell when the concentration of TNF-a increased from 0 up to 10 ngÁmL À1 . The contents of miR-130b increased by 1.09-and by 0.67-fold in Hela and Siha cells after incubated with 10 ngÁmL À1 TNF-a over 48-h time periods as compared with the corresponding contents in cells after incubated with vehicle ( Fig. 2A). To investigate the impact of miR-130b level on the cytotoxicity of TNF-a to target cell, miR-130b inhibitors were transfected into Hela or Siha cells to block the functions of endogenous miR-130bs. After a 48-h incubation time period, the transfection of miR-130b inhibitors resulted in a 24.42% decrease in the viability of Hela and a 11.57% decrease in Siha cell cultured in the medium in the absence of TNF-a but did led to a 29.57% reduction in the viability of Hela and a 16.33% reduction in Siha cell cultured in the medium containing 10 ngÁmL À1 TNF-a as compared with the transfection of the scrambled control oligonucleotides, respectively (Fig. 2B). To determine the impacts of inhibitors on the apoptosis rates of cervical cancer cells, miR-130b inhibitors and their scrambled control oligonucleotides were employed at final concentrations of 100 pmolÁmL À1 in the transfection assays. The transfection of inhibitors increased the apoptosis rate of Hela cell by 0.74-fold and the rate of Siha cell by 0.46-fold when the cell was cultured in the medium without TNF-a but produced a 1.25-fold increment in apoptosis rate of Hela and a 0.69 fold increment of Siha cell when the cell was cultured in the medium involving 50 ngÁmL À1 TNF-a as compared with the transfection of the scrambled control oligonucleotides, respectively (Fig. 2C).

The suppressed expression of PTEN gene caused by TNF-a stimulation rendered cervical cancer cells resistant to TNF-a toxic actions
TNF-a has been previously recorded to suppress the expression of PTEN gene in human colon cell lines [23]. In our research, we got the consistent result in cervical cancer cell. The reductions in the cellular levels of PTEN mRNA as well as the levels of PTEN proteins in the Hela and Siha cells were accompanied with the increases in the concentrations from 0 to 50 ngÁmL À1 of TNF-a (Fig. 3A,B). To explore the impact of PTEN gene expression on the action of TNF-a to the cervical cancer cell, pcDNA3.1::PTEN was transfected into Hela or Siha cell. When the post-transfected cell was incubated in the medium lacking of TNF-a over a 48-h time period, pcDNA3.1::PTEN caused a 19.15% decrease in the viability of Hela cell and a 14.61% decrease in Siha cell, but when the target cell was incubated in the medium containing 10 ngÁmL À1 TNF-a for the same time period, pcDNA3.1::PTEN led to a 22.37% decrease in the viability of Hela cell and a 21.90% decrease in Siha cell when compared with its control vector (Fig. 3C). To explore the impacts of PTEN gene expressions on the apoptosis rates of cervical cancer cells, pcDNA3.1::PTEN vectors and their control vectors were used at final concentrations of 5 lgÁmL À1 in the transfection assays. After the transfected target cells subjected to the same treatments as described above, the apoptosis rates of Hela and Siha cells transfected with pcDNA3.1::PTEN increased by 0.67-and 0.02-fold in the absence of TNF-a stimulation but elevated by 1.44-and 0.25-fold in the presence of TNF-a stimulation (Fig. 3D).

Fig. 2. The TNF-a-induced expression of miR-130b desensitized cervical cancer cell to toxic activity of TNF-a. Cells were incubated with TNF-a at indicated concentrations, and the relative expression levels of miR-130b in target cells were measured in semiquantitative real-time RT-PCR assays at 48 h post-treatments. (A) The incubation of Hela and Siha cells with TNF-a elevated the expression levels of miR-130b. Circles represented the relative levels of miR-130b in TNF-a-treated Hela cells and triangles represented the levels in treated Siha cells as compared with their counterparts in vehicle-treated cells. (B) The transfection of miR-130b inhibitors decreased viabilities of TNF-a-treated
Hela and Siha cells which were determined in MTT assays. (C) The transfection of miR-130b inhibitors increased cell apoptosis rates of TNF-a-treated Hela and Siha cells. The note 'inhibitor' or 'inhibitor control' under the horizontal axis indicated the tumour cell transfected with miR-130b inhibitor or its scrambled control oligonucleotide while 'TNF-a + inhibitor' or 'TNF-a + inhibitor control' indicated the cell with miR-130b inhibitor or its scrambled control oligonucleotide prior to TNF-a treatment. The graphic data describing the apoptosis rates of tumour cells located above the statistical analyses of the graphic data, and the types of oligonucleotides used in the transfection assays were described at the bottom of the graphic data. The blank columns represented the relative levels of cell viabilities or apoptosis rates of Hela cells, and the shadow ones represented the levels or rates of Siha cells. Data were described as means AE SE (n = 3). The bars indicated the deviations from means. The horizontal axis in graphic datum presented the fluorescence intensity of FITC which was conjugated with Annexin-V, and the vertical axis in datum indicated the intensity of propidium iodide (PI) which was used as a DNA stain. *P < 0.05; NS, nonsignificant.

MiR-130b mediated the suppression of PTEN expression caused by TNF-a treatment
The result of the regression analysis showed that the relative expression level of miR-130b in TNF-a-treated cell was inversely correlated with the level of PTEN mRNA (Fig. 4A). We carried out the gain-and loss-of-function assay to test whether there was a causal relationship between the increment in the cellular level of miR-130b and the reduction in the level of PTEN mRNA. The experimental data exhibited that the PTEN mRNA level decreased by 17.48% in Hela and by 13.00% in Siha cell which was transfected with miR-130b mimics in comparison with the corresponding level in the cell transfected with the scrambled control oligonucleotides. After the cell subjected to the treatment of TNF-a at the concentration of 10 ngÁmL À1 over a 48-h time period, the PTEN mRNA level increased by 1.24-fold in Hela and by 0.26fold in Siha cell transfected with miR-130b inhibitors when compared with the counterpart in the cell transfected with the scrambled controls (Fig. 4B). Furthermore, we found there were a 19.14% decrease in the level of PTEN protein in Hela cell and a 15.38% decrease in Siha cell transfected with miR-130b mimics as compared with the corresponding protein levels in the cells transfected with the scrambled control oligonucleotides. The PTEN protein levels in Hela and Siha cells transfected with miR-130b inhibitors increased by 0.32-and 0.21-fold as compared with the corresponding levels in cells with the scrambled control oligonucleotides (Fig. 4C).
MiR-130b suppressed the expression of PTEN gene by directly base pairing with the 3 0 UTR of PTEN mRNA In silico analysis revealed that there were two putative targeted sites of miR-130b existing in the 3 0 UTR of PTEN mRNA (Fig. 5A). To test whether the putative targeted sites were involved in the regulation of PTEN expression by miR-130b, the DNA sequence encoding the UTR encompassing wild-type or mutated targeted site was cloned into the pEGFP vector downstream of the coding domain of GFP gene (Fig. 5B). The constructed vectors were transfected into Hela or Siha cells, and then, the transfected cells were incubated in the medium containing 10 ngÁmL À1 TNF-a over time courses of 48 h. The intensity of the fluorescence emitted by the target cell transfected with pEGFP::wt1-UTRs and pEGFP::wt2-UTRs decreased by 38.98% and by 25.05% in Hela cell and decreased by 22.44% and by 20.64% in Siha cell as compared with the intensity of fluorescence produced by the cell with pEGFP control vectors (Fig. 5C). After the target cell exposed to TNF-a, the transfection of miR-130b inhibitors increased the intensity of fluorescence from the cell with pEGFP::wt1-UTRs and pEGFP::wt2-UTRs by 0.23and 0.21-fold in Hela cell and by 0.13-and 0.08-fold in Siha cell when compared with the transfection of miR-130b inhibitor control oligonucleotides (Fig. 5D). Conversely, the transfection of miR-130b mimics produced the attenuation in the intensity of fluorescence from the cell with pEGFP::wt1-UTRs and pEGFP::wt2-UTRs by 36.37% and 32.96% in Hela cell and by 26.69% and 23.68% in Siha cell when compared with the intensity of fluorescence from the cell with pEGFP control vectors, but no significant change was found between the intensity of fluorescence from the cell with pEGFP::mut1-UTRs or the cell with pEGFP::mut2-UTRs and the intensity from the cell with pEGFP control vectors in either Hela or Siha cell transfected with miR-130b mimics (Fig. 5E).

Discussion
Some specific cell lines are susceptible to toxic actions of TNF-a, but the vast majority of cell lines develop resistances to TNF-a cytotoxicity by different mechanisms. In this study, we observed that two cervical cancer cell lines had no significant loss in the cell viabilities after treated with various concentrations of TNF-a ranging from 0.1 to 50 ngÁmL À1 when compared with vehicle-treated cells (Fig. 1A). The data suggested these cervical cancer cells resistant to the toxicities mediated by TNF-a at these concentrations.
While there was no obvious influence of TNF-a on the viability of tumour cell, the expression level of miR-130b in target cell mounted in response to the increase in the TNF-a concentration ( Fig. 2A). The recent literatures illustrated that NF-jB mediated the TNF-aupregulated expressions of miR-130b in both adipocyte and bladder carcinoma cell lines by directly binding to its response elements within the miR-130b promoters L. Yang et al. miR-130b in TNF-a-stimulated cervical cancer cell [21,22]. And it has been generally known that TNF-a stimulation induced the activation of NF-jB in Hela cell. Based on these facts, we considered that the TNF-a-promoted expression of miR-130b in cervical cancer cell might be through the activation of NF-jB signalling pathway. MiR-130bs have been verified to play oncogenic roles in the developments of different types of cancers. We guessed that the TNF-a-stimulated expression of miR-130b might be involved in the resistance of cervical cancer cell to TNF-a killing. To demonstrate this assumption, we transfected miR-130b inhibitors or their scrambled controls into TNF-a-or vehicle-treated tumour cells. The experimental data showed that blocking endogenous miR-130b produced a decrease in the viability of vehicle-treated cervical cancer cell, but more reduction in the viability was observed in TNF-a-treated counterpart (Fig. 2B). These results presented that miR-130b performed an oncogenic function in cervical cancer cell and TNF-ainduced expression of miR-130b contributed to the resistance of target cell to TNF-a killing. It is well known that TNF-a exerts its toxicity by inducing apoptosis in a variety of cell types. This process can proceed through both the extrinsic apoptosis and the mitochondria-mediated pathway [5]. To see the impact of TNF-a on the apoptosis of cervical cancer cell, we The note 'miR-130b + wt1/2UTR' or 'negative control + wt1/2UTR' under the horizontal axis indicated the tumour cell cotransfected with miR-130b mimics or their scrambled control oligonucleotides and pEGFP::wt1/2UTRs. The note 'miR-130b + mut1/2UTR' or 'negative control + mut1/2UTR' under the horizontal axis indicated the tumour cell cotransfected with miR-130b mimics or their scrambled controls and pEGFP::mut1/2UTRs. Data were described as meansAES. E. (n = 3). The bars indicated the deviations from means. *P < 0.05; NS, nonsignificant.
miR-130b in TNF-a-stimulated cervical cancer cell L. Yang et al. incubated the tumour cell with various concentration of TNF-a but no notable alteration in the apoptosis rate was seen between TNF-a-and vehicle-treated cell (Fig. 1B). However, the transfection of miR-130b inhibitors into the tumour cell prior to TNF-a treatment resulted in the increment in apoptosis rate as compared with the transfection of the scrambled controls of inhibitors (Fig. 2C). These facts indicated that the TNF-a-enhanced expression of miR-130b protected the tumour cell from the apoptosis induced by TNF-a.
The PTEN protein is characterized as a dual-specificity phosphatase and known as a famous tumour suppressor. It modulates cell growth and survival by negatively regulating the phosphoinositide 3-kinase (PI3K)/Akt signalling pathway [24,25]. In the recent decades, the researchers found that the miRNA-regulated PTEN/PI3K/Akt signalling pathway was associated with the drug resistance of tumour cell. MiRNA-21 induced gemcitabine resistance by suppressing the expression of PTEN gene in breast cancer [26]. MiR-221 attenuated the sensitivity of cervical cancer cell to gefitinib through downregulating the PTEN gene expression [27]. MiR-106 triggered cell radioresistance via inhibiting the expression of PTEN gene in colorectal cancer [28]. In our study, we discovered that TNFa stimulation brought about the attenuation in the level of PTEN mRNA as well as protein in cervical cancer cell. Although TNF-a treatment did not cause obvious changes in the viability and apoptosis rate of tumour cell, the overexpression of exogenous PTEN gene in tumour cell produced a reduction in the viability and an elevation in the apoptosis rate of target cell after exposed to TNF-a treatment (Fig. 3A-D). These experimental data suggested that cervical cancer cells should develop their resistances to TNF-a cytotoxicity by suppressing the expression of PTEN gene.
Regression analysis showed that there was an inverse relationship between miR-130b and PTEN mRNA level in cancer cell (Fig. 4A). The transfection of miR-130b inhibitors antagonized the TNF-ainduced downregulation of PTEN mRNA and protein levels, whereas the transfection of miR-130b mimics caused decreases in the cellular levels of both PTEN mRNA and protein (Fig. 4B,C). These evidences presented that there was a causal relationship between the accumulation in miR-130b and the reduction in PTEN mRNA or protein level in cervical cancer cell and supported that miR-130b mediated the TNF-a-stimulated inhibition of PTEN gene expression.
The intensity of fluorescence from the cell with either pEGFP::wt1-3 0 UTRs or pEGFP::wt2-3 0 UTRs was lower than the intensity from the cell with pEGFP control vectors (Fig. 5C). This indicated that the 3 0 UTR region was associated with the downregulation of reporter gene in target cell, and the more loss in the intensity of fluorescence from TNF-a-treated cell than that from vehicle-treated cell showed that the 3 0 UTR region might be involved in the TNF-a-induced suppression of reporter gene expression. As it was proved that TNF-a stimulation increased the level of miR-130b in cervical cancer cell, we assumed that miR-130b must participate in the regulation of reporter gene. And this assumption was supported by the fact that blocking miR-130b function resulted in an increase in the intensity of fluorescence from TNF-atreated cell with either pEGFP::wt1-3 0 UTRs or pEGFP::wt2-3 0 UTRs (Fig. 5D). MiRNA regulate gene expression through complementary binding to 3 0 UTR region of targeted mRNA [29]. Two targeted sites of miR-130b were predicated to locate within the 3 0 UTR of PTEN mRNA, and the transfection of exogenous miR-130b caused an apparent reduction in the expression of reporter gene in the cell containing the pEGFP::wt1-3 0 UTRs or pEGFP::wt2-3 0 UTRs but not in the cell containing pEGFP::mut1-3 0 UTRs or pEGFP::mut2-3 0 UTRs (Fig. 5A,E). These evidences suggested that miR-130b should inhibit the expression of its target gene based on the base pairing between the seed sequence of miR-130b and its complementary region within the 3 0 UTR of targeted mRNA.