Quaking I-5 protein inhibits invasion and migration of kidney renal clear cell carcinoma via inhibiting epithelial-mesenchymal transition suppression through the regulation of microRNA 200c.

BACKGROUND: It has been demonstrated that quaking I-5 protein (QKI-5) plays crucial roles in the metastasis of various kinds of cancers. However, the function and mechanism of QKI-5 in kidney renal clear cell carcinoma (KIRC) metastasis remains unclear. Therefore, this study aimed to explore the mechanism of QKI-5 in the metastasis of KIRC.
METHODS: The expression of QKI-5 was detected using real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) and western blot in KIRC tissues and different cell lines. Immunohistochemical staining was used to detect the quantity of QKI-5 in primary and metastases of KIRC. Cell migration and invasion were measured using wound healing and transwell assays respectively. The quantity of epithelial mesenchymal transition marker proteins was detected using western blot and immunofluorescence staining. The interaction of QKI-5 via microRNA 200c (miR-200c) was confirmed using dual luciferase reporter assay.
RESULTS: Although QKI-5 was significantly more likely to be downregulated in KIRC tissues than that in normal Kidney tissues, it was dramatically elevated in metastatic KIRC tumors. Upregulation of QKI-5 promoted cell migration and invasion and elevated the expression of epithelial-mesenchymal transition (EMT) marker proteins, including vimentin, snail and slug, while it was downregulated for E-cadherin. Furthermore, a dual luciferase reporter assay demonstrated that QKI-5 was a direct target of miR-200c, and that miR-200c could reverse the effect of QKI-5 on cell migration, invasion, and expression of EMT marker proteins.
CONCLUSIONS: Our results revealed that downregulation of QKI-5 by miR-200c attenuated KIRC migration and invasion via the EMT process, indicating that QKI-5 may be a potential therapeutic target and a key indicator of KIRC progression. 2021 Translational Andrology and Urology. All rights reserved.

Introduction

Renal cell carcinoma (RCC), which is derived from renal tubular epithelial cells, ranks second among all types of urinary system malignancies (1). kidney renal clear cell carcinoma (KIRC) is the most common histological type of renal cell carcinoma, accounting for about 70–80% of all RCCs with a very high mortality rate of about 40%. Although significant progress in the diagnosis and treatment of KIRC has been made, the 5-year survival rate of KIRC is less than 10% owing to high recurrence and metastasis rates (2,3). Therefore, research on the mechanism of KIRC metastasis is needed urgently.

RNA-binding protein quaking (QKI) belongs to the conserved signal transduction and activation of RNA (STAR) protein family. It is one of the QKI protein isoforms, which are found mostly in the nucleus and have been proven to play a complex role in tumorigenesis and metastasis in different cancers. It has been demonstrated that QKI-5 suppresses epithelial-mesenchymal transition (EMT) and tumor growth in prostate cancer (4) and inhibits the aggressiveness of lung cancer cells through the inhibiting β-catenin signaling pathway (5). In oral squamous cell carcinoma, QKI-5 inhibits cell proliferation, migration, and invasion in vitro and in vivo (6). However, QKI-5 has been found to promote cell proliferation, invasion, and EMT in esophageal squamous cell carcinoma (7) and in lung cancer, nanoparticle-mediated RNA interference of endothelial QKI expression potently inhibits metastasis (8). In our past research, we investigated the role of QKI in kidney tumorigenesis. We demonstrated that QKI inhibits kidney cancer cell growth in part through the QKI-directed upregulation of RASA1 by directly binding to its QRE region(QKI response element; ACUAAY[N1-20]UAAY) (9), we found that mostly the relative expression level of QKI-5 was significantly lower in the tumour tissues than it was in their noncancerous counterparts, but once the tumor tissue invades into extrarenal adipose tissue, the expression level of QKI-5 will be significantly higher, which suggest QKI-5 may influence tumor invasion, since the function and mechanism of QKI-5 in KIRC metastasis remains unclear, it is necessary to do further investigations of QKI-5 for better understanding the mechanisms of kidney tumor invasion and metastasis.

EMT is a reversible cellular process between epithelial and mesenchymal states (10). To date, increasing evidence has demonstrated that EMT contributes to tumor progression in various cancers, especially in tumor invasion and metastasis (11). EMT is governed by networks of transcriptional and post-transcriptional mechanisms, such as extracellular matrix, adhesion molecules, cytoskeletal proteins transcription factors, and noncoding RNAs (12). In fact, several studies have been demonstrated that QKI-5 affects the EMT process during tumorigenesis. It has been reported that QKI broadly promotes mesenchymal splicing patterns (13), and that QKI-5 expression changes are regulated by microRNAs (miRNAs), such as miR-196b-5p, miR-200/375, miR-574-5p, and miR-221 (14-17). Of these, miR-200c belongs to the miR-200 family and has been demonstrated to be involved in tumor progression by regulating the EMT process in several cancers, such as prostate and colorectal cancer (18-20). In addition, we showed that QKI-5 is dramatically elevated in metastatic KIRC tumors compared to primary KIRC tumors, demonstrating that QKI-5 might be regulated by miR-200c, thus contributing to the metastasis of KIRC. Therefore, we aim to clarify the effects and the mechanism of QKI-5 on KIRC cell invasion, migration, and EMT that contributes to tumor development regulated by miR-200c.

We present the following article in accordance with the MDAR reporting checklist (available at https://dx.doi.org/10.21037/tau-21-833).

Methods

Clinical information

Twenty cases of Matched KIRC tissues and corresponding tumour-adjacent, morphologically normal tissues were collected from 20 KIRC patients seen at the First Affiliated Hospital of Xinjiang Medical University from 2010 to 2016. All the KIRC tissue and corresponding tumour-adjacent, morphologically normal tissues samples were then immediately flash-frozen in liquid nitrogen at −80 °C. Another 20 matched primary KIRC tissues and metastatic KIRC tissues used for immunohistochemical (IHC) staining were obtained from the First Affiliated Hospital of Xinjiang Medical University from 2010 to 2018.

All procedures performed in this study involving human participants were in accordance with the Declaration of Helsinki (as revised in 2013). The project has been approved by the ethics committee of the First Affiliated Hospital of Xinjiang Medical University (No.: 20180213-09), and all of the participants have provided their informed consent.

QKI-5 lentivirus construction, cell culture, and treatment

Lentivirus with overexpressing QKI-5 sequences and sh-QKI-5 sequences was created into pLenO-DCE and pLenR-GPH vectors, respectively. Then, vectors were used to obtain overexpressing QKI-5 and suppressing QKI-5 lentivirus according to the lentivirus packaging instructions. Human clear cell renal cell carcinoma cell lines 786-O and Caki-2, human kidney adenocarcinoma cell line ACHN, human kidney cancer cell lines A-498 and SN12C, human renal papillary cell line SKRC-38, and human renal tubular epithelial cell line HK-2 were purchased from Shanghai Institute of cell biology After cell lines recovery, cells were cultured in 90% Dulbecco’s modified Eagle’s medium (DMEM, 12430054, Gibco, Waltham, MA, USA) supplemented with 10% of fetal bovine serum (FBS, Gibco, Waltham, MA, USA), 100 U/mL penicillin and 100 μg/mL streptomycin at 37 °C in a 5% CO2-contained incubator under 95% saturation humidity. For overexpressing QKI-5 and suppressing QKI-5 lentivirus and transfection, 786-O, ACHN, or Caki-2 cells were seeded in a six-well plate until confluence was reached at 70% to 90%. Then, overexpressing QKI-5 or suppressing QKI-5 lentivirus and the miR-200c NC (non-specific control) and mimics were transiently transfected into 786-O or Caki-2 cells and cultured for 24 h. Next, cells were used for further analysis. The miR-200c and NC mimics were synthesized using RiboBio Co. Ltd. (Guangzhou, China), and sequences were listed at Table S1.

Migration and invasion assays

Cell migration abilities and Cell invasion abilities of 786-O, ACHN, and Caki-2 cells were evaluated using wound healing assays and transwell assays according to previous reports. For wound healing assays, Seed cells in 6 well plates overnight and culture until confluent. Using a (blue) pipette tip make a straight scratch, simulating a wound. Finally discard the media from the wells and add fresh medium to wells. For transwell assays. Briefly, a total of 5×104 suspended 786-O, ACHN, or Caki-2 cells with serum-free media were placed into the upper part of an insert, and subsequently medium with 10% of FBS was added to the lower part. Once the cells had migrated through the membrane after incubation for 24 h, they were fixed with 100% methanol and stained with 0.1% crystal violet. The invasive stained cells and the fixed cells were observed and counted using a light microscope (Olympus, Tokyo, Japan). Three experiments were performed independently.

Quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR)

Total RNA was extracted from cells or tumor tissues using Trizol reagent (Takara, Dalian, China). Two ug of RNA were used to synthesize cDNA using the BestarTM qPCR RT Kit (2221, DBI Bioscience, Newark, DE, USA) and BestarTM miRNA qPCR RT kit (2221, DBI, Bioscience, Newark, DE, USA). Relative QKI-5 or miR-200c levels were measured using qRT-PCR with a 20 μL reaction system, including 10 μL SYBR Mix (Thermo fisher, Waltham, MA, USA), 0.5 μL of each primer (10 μM), 2 μL, cDNA template, and 7 μL RNase ddH2O. ABI PRISM 7500 real-time PCR system (Applied Biosystems, Carlsbad, CA, USA) was used to perform the PCR using the following processes: 95 °C, 5 min; followed by 40 cycles of 94 °C, 30 s, 60°C, 40 s and 72 °C, 15 s. As the internal reference for miR-200c and QKI-5, U6 and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) were used. The fold change of QKI-5 and miR-200c expression was calculated using the 2−ΔΔCt method for at least three biological repeats for each sample. All the primer sequences used are listed in Table S1.

Western blot

Western blot analysis was performed according to the previous report. Briefly, total proteins from 786-O, ACHN, and Caki-2 cells or tumor tissues were extracted using RIPA Lysis buffer (E-BC-R327, Elabscience, Houston, TX, USA) and then the protein concentration was measured using a bicinchoninic acid (BCA) protein assay kit. For western blot, 20 g of protein with protein loading buffer were boiled at 100 °C for 10 min for each sample, followed by separation in 10–12% sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). Then, 5% lipid-free milk buffer were used to block the membranes with blots for 2 h at room temperature after transferring onto polyvinylidene fluoride (PVDF) membranes (Millipore, Billerica, MA, USA), incubated with primary antibody against QKI-5 (ab126742, 1:2,000, Abcam, Cambridge, United Kingdom), E-cadherin (ab40772, 1:1,000, Abcam), vimentin (ab92547, 1:1,000, Abcam, Cambridge, United Kingdom), β-catenin (ab32572, 1:2,000, Abcam, Cambridge, United Kingdom), SNAIL (ab216347, 1:1,000, Abcam, Cambridge, United Kingdom), SLUG (ab51772, 1:1,000, Abcam), and GAPDH (1:2,000, Rabbit polyclonal, Abcam, Cambridge, United Kingdom) overnight at 4 °C. Finally, protein signals were detected using enhanced chemiluminescence (ECL) reagent (Thermo Scientific, Waltham, MA, USA) based on the manufacturer’s instructions. After incubation with secondary antibody anti-mouse immunoglobulin (IgG, ab205719, 1:20,000, Abcam, Cambridge, UK) for 2–3 hours.

Immunohistochemistry

Tumor tissues from different groups were immediately dissected and fixed in 10% buffered formalin and processed in a paraffin tissue processing machine. Sections of 7 μm thickness were stained with haematoxylin and eosin (H&E, G1005, Servicebio, Wuhan, China). Briefly, the specimen was fixed using 10% formaldehyde, and 4 μm serial sections were generated after embedding in paraffin. Slices were inactivated in 3% catalase for 15 min after having been placed in an oven for 1 h at 60 °C. Then, the sections were placed at 37 °C and blocked using 5% bovine serum albumin (BSA) for 30 min. Subsequently, the tumor sections were incubated with KI67 Rabbit Polyclonal antibody (27309-1-AP, 1:500, Proteintech, Rosemont, IL, USA) at 4 °C overnight followed by incubation with biotinylated goat anti-rabbit IgG (ab6721, 1:1,000, Abcam, Cambridge, UK) at 37 °C for 30 min after having been washed with 0.2 mol/L PBS solution (PH 7.4). DAB (K5007, DAKO, Glostrup, Denmark) was used for color rendering, and then the sections were stored at room temperature for 8 min in a dark room. Finally, sections were observed using a XSP-36 microscope (Boshida Optical Co., Ltd, Shenzhen, China).

Bioinformatics analysis

Target miRNAs of QKI-5 were predicted using Targetscan 7.2 (http://www.targetscan.org/vert_72/), Starbase 2.0 (http://starbase.sysu.edu.cn/) and miRWalk (http://mirwalk.umm.uni-heidelberg.de/). online software. Then, QKI-5 and the miRNA expression data were obtained from The Cancer Genome Atlas Program database (TCGA, https://www.cancer.gov/about-nci/organization/ccg/research/structural-genomics/tcga). The correlations between QKI-5 and miRNAs were calculated with Spearman tests using R software (The R Foundation of Statistical Computing, Vienna, Austria). The overall survival for ccRCC patients in T3 or T4 status was determined using the log-rank test.

Dual luciferase reporter assay

TargetScan 7.2 (http://www.targetscan.org) was used to predict the putative targets of miR-200c with 3’UTR of QKI-5. The interaction between miR-200c and 3’UTR of QKI-5 was evaluated using the Dual-Luciferase Reporter Assay System (Promega, Madison, WI, USA) as instructed by the manufacturer. For the 3’UTR of QKI-5, wild and mutant sites were constructed and subcloned into pmirGLO vector. Then, MiR-200c mimic/NC and 3’-UTR of QKI-5 were co-transfected into 293T cells using the Lipofectamine™ 2000 transfection reagents (Cat. #52887, Invitrogen, Carlsbad, CA, USA). Cells were washed twice with phosphate buffered saline and lysed using the passive lysis buffer at 48 hours after transfection. Luciferase activity was evaluated using the Dual-Luciferase Reporter Assay System (Promega, Madison, WI, USA) according to the manufacturer’s instruction. Primers used for vector construction are listed in Table S1.

Statistical analysis

All data are shown as means ± standard deviations (SD) and were analyzed using SPSS 21.0 (SPSS, Inc., Chicago, IL, USA) software. One-way analysis of variance (ANOVA) was followed by Dunnett’s multiple comparison tests and student’s t-tests to assess the statistical significance of the differences between treatment groups. P<0.05 was considered as indicating statistical significance.

Results

Characteristic of QKI-5 in KIRC

It has been proven that QKI-5 is downregulated in KIRC samples corresponding to noncancerous normal tissues. Consistent with these results, qRT-PCR and western blot analysis showed that the expression of QKI-5 was significantly downregulated in KIRC tissues compared to normal kidney tissues (). However, we found that the expression of QKI-5 was dramatically elevated in metastatic KIRC compared to primary KIRC using immunohistochemical staining (), suggesting that QKI might play crucial roles in the metastasis of KIRC. Further analysis showed that lower QKI-5 expression level demonstrated better overall survival during both the T3 and T4 periods of KIRC ().

Figure 1

Characteristic of QKI-5 in clear cell renal cell carcinoma (ccRCC). (A) Real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to detect the expression of QKI-5 in normal and ccRCC tissues (n=20). (B,C) Expression of QKI-5 was detected using western blot in normal and kidney renal clear cell carcinoma (KIRC) tissues (n=6) and relative grey density was calculated using image J. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) acted as a control. (D) Immunohistochemical staining analysis for QKI-5 in primary and metastatic ccRCC tissues (n=20; ×200). (E,F) Overall survival analysis of QKI-5 expression in ccRCC patients during the T3 and T4 periods. Data are shown as mean ± SD. **, P<0.01, ccRCC group vs. normal group.

Elevated expression of QKI-5 in ACHN cells compared to HK-2 cells

To understand the function of QKI-5 in KIRC, the expression of QKI-5 in different kidney cells was investigated using qRT-PCR and western blot. As show, compared with HK-2 cells (human renal tubular epithelial cells), the expression of QKI-5 was significantly elevated in ACHN cell (cell line which was initiated from malignant pleural effusion of metastatic renal adenocarcinoma) while it was downregulated in SN-12C, SKRC-39, A-498, Caki-2, and 786-0 cells. To assess the expression levels of cell cultures, a suppressing QKI-5 ACHN cell line, an overexpressing the QKI-5 Caki-2 cell line, and overexpressing and suppressing QKI-5 786-0 cells were generated and used for further study. As shows, QKI-5 was successfully downregulated in ACHN and 786-0 cells and upregulated in 786-0 and Caki-2 cell lines, suggesting that these cell lines could be used for further analysis.

Figure 2

The expression of QKI-5 was elevated in ACHN cells compared to HK-2 cells. (A) Relative expression of QKI-5 in different cell lines detected using real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR), including HK-2, ACHN, SN-12C, SKRC-39, A-498, Caki-2, and 786-0 cell lines; (B) expression of QKI-5 in different cell lines detected using western blot; (C) Relative grey density of QKI-5 were calculated using image J; (D-F) relative expression changes of QKI-5 detected using qRT-PCR in 786-0, ACHN, and Caki-2 cells with QKI-5 overexpression or suppression; (G) Relative expression changes of QKI-5 detected using western blot in 786-0, ACHN, and Caki-2 cells with QKI-5 overexpression or suppression. (H) Relative grey density of QKI-5 were calculated using image J; Data are shown as mean ± SD, glyceraldehyde 3-phosphate dehydrogenase (GAPDH) acted as control. *, P<0.05; **, P<0.01 vs. HK-2 in (A) or vs. sh-QKI-5-NC group in (C,D,G); ##, P<0.01 vs. Over-QKI-5-NC group in (C,E,G).

Upregulation of QKI-5 promotes cell migration and invasion

To understand the effect of QKI-5 on the progression of KIRC, migration and invasion were detected in 786-0, ACHN, and Caki-2 cell lines through overexpressing or suppressing the expression of QKI-5. As show, invasion was significantly blocked in the sh-QKI-5-1 group compared with the sh-QKI-5-NC group, while it was enhanced in the Over-QKI-5 group compared with the Over-QKI-5-NC group in 786-0 cells. The migration ability detection results showed that the migration rate of the 786-0 cells was significantly decreased when suppressing QKI-5 expression, while it was dramatically increased when overexpressing QKI-5 expression in 786-0 cells (). In addition, downregulation of QKI-5 expression in ACHN cells significantly decreased the invasion and migration ability of ACHN cells, while upregulation of QKI-5 expression in Caki-2 cells significantly elevated the invasion and migration ability of Caki-2 cells (). These results demonstrate that upregulation of QKI-5 promotes cell migration and invasion.

Figure 3

Upregulation of QKI-5 promotes cell migration and invasion. (A) Transwell assay was used to detect the effect of QKI-5 on the invasion of 786-0 cells; Cells with serum-free media were placed into the upper part of an insert, and subsequently medium with 10% of FBS was added to the lower part. Once the cells had migrated through the membrane after incubation for 24 h, they were fixed with 100% methanol and stained with 0.1% crystal violet. The cells were counted in 5 randomly selected microscopic fields (×200) from each chamber. (B) Number of 786-0 cells in different groups calculated using image J. (C) Wound healing assay was used to detect the effect of QKI-5 on migration rate changes in 786-0 cells. Uniform artificial wounds were made at 2 d after transfection and the cells were cultured for another 24 h. Cell migration ability was represented by the wound gap distance in microscopic field (×40) at the time points of 0 and 24 h. The migration rates are shown in (D). (E) Effect of QKI-5 on the invasion of ACHN and Caki-2 cells with QKI-5 inhibition and overexpression (F) number of ACHN and Caki-2 cells in different groups calculated using image J. (G) Effect of QKI-5 on migration rates changes in with QKI-5 inhibition and overexpression, and the migration rates of ACHN and Caki-2 cells in different groups are shown in (H). Data are shown as mean ± SD. *, P<0.05; **, P<0.01, sh-QKI-5-NC group vs. Sh-QKI-5-1 group; ##, P<0.01, Over-QKI-5 group vs. Over-QKI-5-NC group.

QKI-5 affects the expression of EMT marker genes

It has been demonstrated that QKI-5 participates in the EMT process in several cancers, such as head and neck squamous cell carcinoma (HNSCC). To understand the effect of QKI-5 on the EMT process in KIRC, the expression of several EMT-related genes was investigated, including E-cadherin, vimentin, β-catenin, snail and slug. The results showed that the expression of QKI-5 was overexpressed in 786-0 and Caki-2 cells and successfully suppressed in 786-0 and ACHN cells (). Further analysis showed that the expression of vimentin snail and slug was significantly increased both in overexpressing 786-0 cells and Caki-2 cells, while it was significantly decreased in suppressing 786-0 and ACHN cells. However, the expression changes of E-cadherin showed the opposite results in different cell lines (). In addition, no expression changes of β-Catenin were observed in different groups ().

Figure 4

QKI-5 affected the expression of epithelial-mesenchymal transition (EMT) marker genes. (A) Western blot was used to detect the expression of EMT marker genes affected by QKI-5, and relative grey density was calculated using image J. (B) This included E-cadherin, vimentin, β-catenin, snail and slug. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) acted as control. Data are shown as mean ± SD. **, P<0.01, sh-QKI-5-NC group vs. Sh-QKI-5-1 group; ##, P<0.01, Over-QKI-5 group vs. Over-QKI-5-NC group.

QKI-5 was regulated by miR-200c

MicroRNA regulation of tumor-related genes is one of the most important regulatory patterns in the process of tumor growth. To understand the miRNAs which directly target QKI-5, QKI-5-targeted miRNAs were investigated using Targetscan, Starbase, and miRWalk. In total, from the three databases, 304 common miRNAs were predicted to bind with QKI-5 directly (). Further analysis showed that there were six miRNAs that showed negative correlations with QKI-5 using KIRC data from TCGA. and miR-200c, which showed the most negative correlations, including miR-200c (r=−0.592), miR-96-5p (r=−0.368), miR-429 (r=−0.366), miR-200b-3p (r=−0.347), miR-141-3p (r=−0.320), and miR-4784 (r=−0.307) (). Therefore, miR-200c was selected for further analysis. It showed that the expression of miR-200c was significantly upregulated in KIRC tissues compared with normal tissues (). Furthermore, it showed that a binding site (UAAGACA) existed of miR-200c in the 3’UTR of QKI-5 (). A dual-luciferase reporter assay showed that compared with the NC (non-specific control) group, the expression of luciferase was significantly inhibited in the QKI-5 wild-type group when supplemented with miR-200c mimic, while there was no significant difference in the expression of luciferase, when the miR-200c binding sites of QKI-5 were mutated (). These results demonstrate that QKI-5 is one of the directly binding targets for miR-200c.

Figure 5

QKI-5 was regulated using microRNA 200c (miR-200c). (A) Target miRNAs of QKI-5 predicted by Targetscan 7.2, Starbase and miRWalk. (B) Top 20 miRNAs showed negative correlations with the expression of QKI-5 from the Cancer Genome Atlas (TCGA). (C) Correlation between the expression of QKI-5 and miR-200c. (D) Relative expression of miR-200c in normal and clear cell renal cell carcinoma (ccRCC) tissues detected by real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR). (E) The binding sites of miR-200c in 3’UTR of QKI-5. (F) Dual-luciferase reporter assay to detect the regulation of miR-200c to QKI-5 by binding with 3’UTR of QKI-5. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) acted as control. Data are shown as mean ± SD. *, P<0.05, mir-200c group vs. NC group.

Upregulation of miR-200c suppressed cell invasion and migration in 786-0 and Caki-2 cell lines

Functional analysis of miR-200c to cell invasion and migration in 786-0 and Caki-2 cell lines showed that upregulation of miR-200c inhibited the invasion and migration ability in 786-0 and Caki-2 cell lines (). In addition, upregulation of miR-200c attenuated the elevation of invasion and migration ability in 786-0 and Caki-2 cell lines caused by QKI-5 overexpression (). These results demonstrate that upregulation of miR-200c suppressed cell invasion and migration in 786-0 and Caki-2 cell lines by targeting QKI-5.

Figure 6

Upregulation of microRNA 200c (miR-200c) suppressed cell invasion and migration in 786-0 and Caki-2 cell lines. (A) Transwell assay was used to detect the effect of microRNA 200c (miR-200c) on the invasion of 786-0 and Caki-2 cell lines (stained with crystal violet, ×200); (B) Number of 786-0 and Caki-2 cells in different groups calculated using image J; (C) wound healing - assay was used to detect the effect of miR-200c on migration rate changes in 786-0 and Caki-2 cell lines, Uniform artificial wounds were made at 2 d after transfection and the cells were cultured for another 24 h. Cell migration ability was represented by the wound gap distance in microscopic field (×40) at the time points of 0 and 24 h. and the migration rates are shown in (D). Data shown as mean ± SD. **, P<0.01, miR-200c-NC mimic group vs. miR-200c-NC group; #, P<0.05; ##, P<0.01, QKI-5+miR-200c mimic group vs. QKI-5+miR-200c NC group.

Upregulation of miR-200c changes the expression of EMT marker genes

Western blot analysis showed that the expression of vimentin, snail and slug was significantly decreased, while the expression of E-cadherin was significantly upregulated when miR-200c was added to 786-0 and Caki-2 cells. However, the expression of β-catenin was not affected by miR-200c mimic (). In addition, the expression changes of vimentin, E-cadherin, snail and slug were partially reversed when miR-200c mimics were added to overexpressing QKI-5 786-0 and Caki-2 cells (). The expression changes of vimentin, E-cadherin and β-catenin in different groups were also confirmed using immunofluorescence analysis in the 786-0 and Caki-2 cells ().

Figure 7

Upregulation of microRNA 200c (miR-200c) changed the expression of epithelial-mesenchymal transition (EMT) marker genes. (A) Relative expression of EMT marker genes detected by western blot in 786-0 and Caki-2 cell lines treatment with miR-200c mimic; (B,C) relative grey density of EMT marker genes in 786-0 and Caki-2 cell lines; (D) immunofluorescence staining analysis for E-cadherin, vimentin, and β-catenin in 786-0 and Caki-2 cell lines treatment with miR-200c mimic (×200), glyceraldehyde 3-phosphate dehydrogenase (GAPDH) acted as control. Data are shown as mean ± SD. **, P<0.01, miR-200c-NCmimic group vs. miR-200c-NC group; #, P<0.05; ##, P<0.01, QKI-5+miR-200c mimic group vs. QKI-5+miR-200c NC group.

Discussion

Clear cell renal cell carcinoma is one of the most common types of malignant tumors, and it is difficult to diagnose early and to treat, with high rates of mortality, metastasis and recurrence in patients (21). Although significant progress has been made in the diagnosis and treatment of KIRC, 20–30% patients present with metastases to the lungs, brain, and other organs (22,23). A large number of genes have been discovered, including noncoding RNAs or signal pathways that are closely related to the occurrence and development of KIRC (24). The protein QKI-5 belongs to the signal transduction and activation of RNA (STAR) protein family, and it is also a key post-transcriptional regulator. It exhibits dual functions in various kinds of cancers by acting as an oncogene or anti-oncogene. For example, QKI-5 suppresses proliferation of oral squamous cell carcinoma cells via the MAPK and β-catenin signaling pathways (25). However, upregulation of QKI-5 promotes cell proliferation, migration, and invasion of esophageal squamous cell carcinoma cells (7). It has been demonstrated that in approximately 25% of KIRC patients the loss of RNA-binding protein QKI at 6q26 (26) is involved, suggesting that QKI plays crucial roles in KIRC. We have demonstrated that QKI-5 is frequently downregulated in KIRC patients, and its downregulation is significantly associated with clinical features including tumor (T) status, metastasis (M) status, differentiation grade, and poorer patient prognosis (9). However, at the same time, once the tumor infiltrates into the extra capsular adipose tissue of kidney, the expression of level of QKI-5 mRNA is significantly higher than that of the adjacent normal tissue. In the present study, further analysis of QKI-5 showed that the expression of QKI-5 is significantly upregulated in metastatic KIRC compared to that in primary foci, and it also shows higher expression in ACHN cells than that in HK-2. We also know that ACHN cells originate from metastatic renal adenocarcinoma, suggesting that QKI-5 might be a key regulator in the metastasis of KIRC. The overall survival analysis of T3 and T4 status of KIRC patients showed that lower QKI-5 expression improved overall survival. These results demonstrate that QKI-5 plays important roles in the metastasis of KIRC. However, the exact role of QKI-5 in KIRC metastasis is unknown. In the present study, we showed that overexpressing QKI-5 promotes invasion and migration in 786-0 and Caki-2 cells while suppressing QKI-5-inhibits invasion and migration in 786-0 and ACHN cells, indicating that QKI-5 promotes metastasis of KIRC. Mostly in our opinion, the expression of a gene was downregulated in tumor tissue, and the downregulation of the gene improved migration and invasion, but in our current research, the increased expression QKI-5 promoted cell migration and invasion, we think it’s an interesting phenomenon. Maybe it was the gene complicated function in the different stage of the disease, as we know, being an RNA binding protein, QKI-5 can directly bind to and regulates hundreds of alternative splicing targets and exerts pleiotropic effects, such as cell growth, migration and invasion, which deserve our further more research.

MicroRNAs are highly conserved single-stranded non-coding small RNA, which are composed of 19 to 25 nucleotides. The regulatory function of miRNA on the expression of related target genes is mainly achieved through posttranscriptional gene silencing by binding 3’UTR of the target genes. In recent years, miRNAs have been found to be closely associated with the outcome of the patients with KIRC by affecting cancer cell proliferation, differentiation, apoptosis, invasion, and metastasis, such as miR-508, miR-337-3p, and miR-663 (27,28). MicroRNA-663 inhibits the proliferation and invasion of clear cell renal cell carcinoma cells by directly targeting PAK4. Several miRNAs have also become potential biomarkers of KIRC such as miR-205 and miR-210 (29-31). MicroRNA 200c belongs to the miR-200 family, which has been demonstrated to participate in the development of KIRC via affecting different cell processes and metastasis (32). The miR-200 family has been considered to be a prognostic marker in KIRC (33). In addition, some target genes of miR-200c have also been investigated, including CDK2, CYP1B1, SLC6A1, and heme oxygenase-1 (34-37). Pillman et al. demonstrated that miR-200c and miR-375 regulate epithelial plasticity-associated alternative splicing by repressing QKI-5 (16). Consistent with this result, we showed that miR-200c has a negative correlation with QKI-5 and is a direct target of miR-200c. Further analysis showed that overexpression miR-200c attenuates the effect of invasion and migration caused by QKI-5 both in 786-0 and Caki-2 cells. These results demonstrate that QKI-5 suppression via the regulation of miR-200c inhibits invasion and migration of KIRC.

Deregulated EMT constitutes one of the major aspects of cancer progression. Studies have confirmed that EMT play an important role in tumor invasion and metastasis. During EMT, QKI-5 directly binds to and regulates hundreds of alternative splicing targets, which play crucial roles in tumor growth (13), suggesting QKI-5 can affect metastasis of epithelium-derived cancers. Several studies have demonstrated that QKI-5 can promote the EMT process. For example, MiR-143-3p inhibits cell proliferation, invasion, and EMT by targeting QKI-5 in esophageal squamous cell carcinoma (ESCC) (7). Inhibition of QKI-5 suppresses migration, invasion, and TGF-β1-induced EMT of lung cancer cells (5). Consistent with previous studies, in our study, we found that overexpressing QKI-5 can promote the EMT process by elevating the expression of vimentin, snail, slug and downregulating E-cadherin in ccRCC cells. In addition, a number of studies have demonstrated that miR-200c acts as a tumor suppressor involved in the inhibition of tumor metastases by repressing the EMT process. For example, tamoxifen reverses EMT by demethylating miR-200c in triple-negative breast cancer cells (38), and nicotine promotes metastasis and EMT in human colorectal cancer cells by downregulating miR-200c (20). Also, miR-200c has been found to be involved in the process of mesenchymal-to-epithelial transition (MET) during renal development. For example, the entire miR-200 seed family is strongly deregulated in ccRCC compared to proximal tubular epithelial cells of the kidney (39). Also, miR-200c modulates the EMT in human renal cell carcinoma metastasis by affecting the Akt-miR-200c-E-cadherin axis (40). In the present study, we found that miR-200c attenuates the effect of QKI-5 on the expression of vimentin, snail, slug and E-cadherin, demonstrating that suppression of QKI-5 inhibited the EMT process via regulation by miR-200c. Taken together, we demonstrated that QKI-5 inhibited by miR-200c attenuated invasion and migration via inhibiting the EMT process in KIRC. However, more systematic clinical experiments need to be designed and performed to provide a reliable basis for clinical diagnosis and targeted therapy of KIRC.

Conclusions

In summary, the present study revealed that suppressing QKI-5 inhibits invasion and migration of KIRC via inhibiting EMT transition regulated by miR-200c, suggesting that QKI-5 may be a potential marker and therapeutic target of renal clear cell carcinoma metastasis.

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