MiR-26a/miR-26b represses tongue squamous cell carcinoma progression by targeting PAK1
Cancer Cell International volume 20, Article number: 82 (2020)
Tongue squamous cell carcinoma (TSCC) is the most common oral malignancy. Previous studies found that microRNA (miR)-26a and miR-26b were downregulated in TSCC tissues. The current study was designed to explore the effects of miR-26a/miR-26b on TSCC progression and the potential mechanism.
Expression of miR-26a, miR-26b and p21 Activated Kinase 1 (PAK1) in TSCC tissues and cell lines was detected by reverse transcription- quantitative polymerase chain reaction (RT-qPCR). Flow cytometry analysis was performed to examine cell cycle and apoptosis. Transwell assay was conducted to evaluate the migrated and invasive abilities of SCC4 and Cal27 cells. In addition, western blot assay was employed to analyze the protein level. Glucose assay kit and lactate assay kit were utilized to analyze glycolysis. Dual-luciferase reporter and RNA immunoprecipitation (RIP) assays were applied to explore the relationship between miR-26a/miR-26b and PAK1. Xenograft tumor model was constructed to explore the role of miR-26a/miR-26b in vivo.
Both miR-26a and miR-26b were underexpressed, while PAK1 was highly enriched in TSCC. Overexpression of miR-26a and miR-26b inhibited TSCC cell cycle, migration invasion and glycolysis, while promoted cell apoptosis. Both miR-26a and miR-26b directly targeted and negatively regulated PAK1 expression. Introduction of PAK1 partially reversed miR-26a/miR-26b upregulation-mediated cellular behaviors in TSCC cells. Gain of miR-26a/miR-26b blocked TSCC tumor growth in vivo.
MiR-26a/miR-26b repressed TSCC progression via targeting PAK1 in vitro and in vivo, which enriched our understanding about TSCC development and provided new insights into the its treatment.
MiR-26a and miR-26b are downregulated.
Upregulation of miR-26a/miR-26b represses cell cycle, migration, invasion and glycolysis, while promotes cell apoptosis of TSCC cells in vitro.
PAK1 is upregulated in TSCC.
Both miR-26a and miR-26b target PAK1.
MiR-26a/miR-26b inhibits TSCC progression by targeting PAK1.
Introduction of miR-26a/miR-26b blocks TSCC tumor growth in vivo.
TSCC is the most familiar form of oral cancer, with quick progress plus easy metastasis, which usually causing trouble of chew, speech and ingurgitation [1, 2]. There were approximately 48,100 new cases and 22,100 deaths related to TSCC in China in 2015 . Despite treatment options for TSCC got greatly improved, like surgical excision, chemotherapy and radiotherapy, the treatment outcome of patients with TSCC was still very poor . Therefore, it is necessary to explore mechanisms involved in the progression of TSCC so as to develop new therapeutic approaches for TSCC patients.
MicroRNAs (miRNAs) are highly conserved ncRNAs with approximately 22 nucleotides that can play vital regulatory roles in animals and plants by targeting message RNAs (mRNAs) for cleavage or translational inhibition . It was determined that certain miRNAs participated in cellular behaviors, such as cell-cycle regulation, inflammation, stress response, migration, invasion, differentiation and apoptosis . Dysregulation of miRNAs is commonly observed in diverse tumors, including TSCC, and closely related to cancer progression, functioning as either tumor oncogenes or suppressors [7, 8]. MiR-26a and miR-26b make up the miR-26 family . MiR-26a and miR-26b are commonly dysregulated in various cancers, as well as involve in multiple biological processes via targeting corresponding mRNAs [10, 11]. Previous studies indicated that the expression of miR-26a and miR-26b was downregulated in tongue squamous cell carcinoma [11, 12]. However, the definite molecular mechanism of miR-26a/miR-26b related to TSCC progression needs further investigation.
PAKs are a group of serine/threonine kinases that function as downstream nodes for kinds of oncogenic signaling pathways; among which PAK1 locates at 11p13 region . Additionally, PAKs have been involved in certain pathological conditions, including cancer . Upregulation of PAK1 was reported in diverse human cancers, such like thyroid cancer , ovarian cancer , bladder cancer  and TSCC . Through bioinformatic analysis, we observed that PAK1 could bind with miR-26a/miR-26b. Nevertheless, the potential mechanism of PAK1 in miR-26a/miR-26b-mediated TSCC calls for deeper investigation.
In our study, we investigated the influence of miR-26a/miR-26b on cell cycle, migration, invasion, glycolysis and apoptosis of TSCC in vitro and on tumor propagation in vivo, as well as explored underlying molecular mechanism.
Materials and methods
Patients and tumor tissues
44 paired TSCC tumor tissues and matched normal tissues were collected from patients with TSCC at the Luoyang Central Hospital Affiliated to Zhengzhou University, which were diagnosed and received tumor resection surgery between 2016 and 2018. All patients did not undergo radiotherapy, chemotherapy or other targeted therapy before surgery. All tissues were immediately put into liquid nitrogen after collection and kept at − 80 °C. This study got approval of the Ethics Committee of the Luoyang Central Hospital Affiliated to Zhengzhou University and each patient offered the written informed consent.
Cell culture and transient transfection
Cal27, SCC4 and SCC9 cells as well as 293T cells were obtained from ATCC (Manassas, VA, USA). UM1 cells were purchased from Japanese Collection of Research Bioresources (JCRB) cell bank (Osaka, Japan), and normal human oral keratinocyte (NHOK) was supplied by ScienCell Research Laboratories (San Diego, CA, USA). Above cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, PAN Biotech, Aidenbach, Germany) added with fetal bovine serum (FBS; 10%, HyClone, Logan, UT, USA) at 37 °C with 5% CO2.
Mimic of miR-26a (miR-26a) or miR-26b (miR-26b) and the mimic negative control (miR-NC), inhibitors of miR-26a (anti-miR-26a) or miR-26b (anti-miR-26b) and the inhibitor negative control (anti-miR-NC) and pcDNA-PAK1 (PAK1) were acquired from GenePharma Co., ltd. (Shanghai, China). And the pcDNA empty vector (pcDNA) was purchased from Thermo Fisher Scientific (Waltham, MA, USA). SCC4 and Cal27 cells were sowed into 6-well plates (about 2 × 106 cells/well) and transfected with aforementioned nucleotides or plasmids when confluence reached 70–80% using Lipofectamine 2000 (Life Technologies Corporation, Carlsbad, CA, USA) referring to manufacturer’s recommendations.
The total RNA was isolated from tissues or transfected cells with miRNeasy Mini Kit (QIAGEN, Hilden, Germany). As for the detection of miR-26a and miR-26b enrichment, TaqMan reverse transcription kit and TaqMan MicroRNA Assays (Thermo Fisher Scientific) were employed to conduct reverse-transcription and qPCR, and U6 served as an internal control. For PAK1 abundance detection, total RNA was extracted using TRIzol® reagent (Solarbio, Beijing, China). And complementary DNA was generated using M-MLV Reverse Transcriptase (Solarbio). 2× SYBR Green PCR Mastermix (Solarbio) was used to evaluate the mRNA level of PAK1, with Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as an internal reference. The relative expression levels were assessed using the 2−∆∆Ct method. Primers sequences used were listed as below: miR-26a-forward (F), 5′-CTCAACTGGTGTCGTGGAGTCGGCAATTCAGTTGAGAGCCTATC-3′, miR-26a-reverse (R), 5′-ACACTCCAGCTGGGTTCAAGTAATCCAGGATA-3′; miR-26b-F, 5′-CCGGGACCCAGTTCAAGTAA-3′, miR-26b-R, 5′-CCCCGAGCCAAGTAATGGAG-3′; U6-F, 5′-CTCGCTTCGGCAGCACA-3′, U6-R, 5′-AACGCTTCACGAATTTGCGT-3′; PAK1-F, 5′-GGTGGTGGCTGCACAGTAG-3′, PAK1-R, 5′- TCTGAGGCAGGAGGTGGTAA-3′; GAPDH-F, 5′-AATCCCATCACCATCTTCC-3′, GAPDH-R, 5′-CATCACGCCACAGTTTCC-3′.
Cell cycle assay
Transfected SCC4 and Cal27 cells were gathered, washed with pre-cold PBS and fixed with 70% ethanol. Following overnight incubation, cells were washed and stained with propidium iodide reagent in the dark. The distribution of cells in G0-G1, S and G2-M phases was determined by a flow cytometer (Countstar, Shanghai, China).
To measure migration, transfected SCC4 and Cal27 cells (1 × 105) were seeded in DMEM in the higher portion of each chamber (8 µm; Corning Inc., Corning, NY, USA), while DMEM with 10% FBS was put into the lower portion of each chamber. After 48 h, cells sticking to the base of the higher portion were stained with 0.1% crystal violet, then photographed and counted using X-71 inverted light microscope (Olympus, Tokyo, Japan). Invasion assay was implemented using the similar protocols but instead, the upper compartment was coated with Matrigel (Corning Inc.) and dried overnight under sterile condition.
Transfected SCC4 and Cal27 cells were gathered, washed twice with pre-cold PBS and resuspended in 200 µL binding buffer. Then Annexin V-FITC Apoptosis Detection Kit (Beyotime, Shanghai, China) was applied to evaluate apoptotic cells according to the manufacturer’s instructions. Apoptotic rates were determined utilizing a flow cytometer (Countstar) based on the analysis of the proportion of cells at Annexin V+/PI±.
Western blot analysis
Western blot analysis was applied to analyze the protein levels of matrix metalloproteinase 9 (MMP9, cell migration marker), Cyclin D1 (CCND1, cell cycle marker), Proliferating Cell Nuclear Antigen (PCNA, cell proliferation marker), B-cell lymphoma-2 (Bcl-2, cell apoptosis marker), Bcl-2-Associated X (Bax, cell apoptosis marker) and PAK1. Firstly, total protein was isolated from SCC4 and Cal27 cells using Radio-Immunoprecipitation Assay buffer (Beyotime). Then extracted samples (30 µg/lane) were loaded onto 12% sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) gels and then transferred onto polyvinylidene difluoride membrane (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The membranes were saturated with 5% non-fat milk for 2 h, and incubated with specific antibodies against MMP9 (1:1500 dilution, HPA001238), CCND1 (1:1000 dilution, HPA027802), PCNA (1:1500, SAB4502103), Bax (1:1000 dilution, SAB4502546), Bcl-2 (1:1000 dilution, SAB4500003), PAK1 (1:1000 dilution, SAB4502065) or anti-β-actin (1:3000 dilution, SAB5500001) at 4 °C overnight, respectively; followed by incubation with corresponding secondary antibody (1:10,000 dilution, 12-348) for 2 h. Protein blots were motivated using ECL western blot detection system (Millipore, Billerica, MA, USA), with β-actin as a control. Above antibodies were acquired from Sigma (Saint Louis, Missouri, USA). All uncropped immunoblot images with molecular weight markers were displayed in Additional files 1, 2, 3, 4.
Glucose consumption and lactate production analysis
Glycolysis could be assessed by glucose consumption and lactate production. At 48 h post transfection, the medium, SCC4 and Cal27 cells were gathered, and the content of glucose and lactate in medium was analyzed by the usage of the glucose assay kit (Biovision, Milpitas, CA, USA) and lactate assay kit (Biovision) in conformity to the supplier’s instructions.
The prediction of potential target mRNAs of miR-26a/miR-26b was conducted using the convincing online prediction website DIANA TOOL (http://carolina.imis.athena-innovation.gr/diana_tools/web/).
Dual-luciferase reporter assay
Then the 3′UTR segments of PAK1 harboring the binding sites for miR-26a and miR-26b (the same two) were amplified by PCR and subcloned into the pGL3 luciferase promoter vector (pGL3-empty, Promega, Madison, WI, USA), signed as PAK1-WT1 and PAK1-WT2, respectively. In addition, their mutants obtained by mutating the binding sites were also amplified and subcloned into the vector to construct corresponding PAK1-MUT1 and PAK1-MUT2, respectively. Then, 293T cells were co-transfected with PAK1-WT or PAK1-MUT, along with miR-26a, miR-26b or miR-NC utilizing Lipofectamine 2000 (Life Technologies Corporation). After 48 h, the luciferase activities were assessed via Dual-Luciferase Reporter System (Beyotime) following the protocols of manufacturer.
The commercial EZ-Magna RIP Kit (Millipore) was applied for the RIP assay. SCC4 and Cal27 cells were harvested when confluence reached 80% and then lysed using pre-coat RIP lysis buffer. The extract was then incubated with anti-Ago2 or anti-IgG (Sigma). After overnight incubation, proteinase K was used to digest the protein in the samples, and the immunoprecipitated RNA was isolated, purified and subjected to RT-qPCR assay.
Xenograft tumor assay
The experiment in nude mice was permitted by the Ethics Committee of the Luoyang Central Hospital Affiliated to Zhengzhou University. 20 male BALB/c nude mice (4–6-week-old) were purchased from Beijing Laboratory Animal Center (Beijing, China) and evenly divided into four groups (n = 5). SCC4 cells stably introduced with nothing (Empty group), miR-NC (miR-NC group), miR-26a (miR-26a group) and miR-26b (miR-26a group) were injected into the right flank of nude mice. The volume of formed tumors was monitored once a week using the formula, Volume = length × width2/2. 4 weeks later, all mice were killed to resect the tumors, then tumors were weighed.
All data were derived from at least 3 repetitions and shown as mean ± standard deviation and analyzed utilizing SPSS 21.0 software (SPSS, Chicago, IL, USA). The comparison was executed using Student’s t-test or one-way analysis of variance followed by Tukey test. P less than 0.05 was recognized as statistically significant.
Both miR-26a and miR-26b were downregulated in TSCC tissues and cell lines
The expression levels of miR-26a and miR-26b in 44 pairs of TSCC tissues (tumor tissue) and adjacent normal tissues (No-tumor tissue) were initially detected using RT-qPCR. We found that both miR-26a and miR-26b expression were significantly decreased in TSCC tissues, when compared with normal tissues (Fig. 1a, b. P < 0.0001; P < 0.0001), in concordance with the analysis result utilizing YM500v and starbase 3.0 (Additional file 5). Moreover, we also examined the expression of miR-26a and miR-26b in TSCC cell lines (Cal27, SCC4, SCC9 and UM1) and NHOK. As compared with NHOK cells, the four cell lines all showed apparently reduced expression of miR-26a and miR-26b (Fig. 1c, d. P = 0.0006, P = 0.0014, P = 0.0068, P = 0.0312; P = 0.0007, P = 0.0003, P = 0.0101, P = 0.00237).
Overexpressed miR-26a and miR-26b repressed TSCC cell cycle, migration and invasion
To clarify the function of miR-26a and miR-26b in TSCC progression, SCC4 and Cal27 cells with miR-26a and miR-26b overexpression were constructed by transfection with miR-26a mimic or miR-26b mimic, respectively. Following RT-qPCR assay was employed to confirm the transfection efficiency and witnessed an about fivefold increasement of the expression of miR-26a/miR-26b, revealing that both miR-26a and miR-26b expression were highly enriched in transfected SCC4 and Cal27 cells (Fig. 2a, b. P = 0.0001, P = 0.0002; P = 0.0003, P < 0.0001). Flow cytometry assay showed that overexpression of miR-26a and miR-26b repressed the cell cycle of treated SCC4 and Cal27 cells, causing almost half reduction (Fig. 2c, d. P = 0.0065, P = 0.0049, P = 0.0059, P = 0.0032; P = 0.0035, P = 0.0056, P = 0.0036, P = 0.003). Moreover, Transwell assay indicated that the migrated and invasive abilities of miR-26a/miR-26b-overexpressed TSCC cells were obviously decreased when compared with the cells transfected with miR-NC (Fig. 2e–h. P = 0.0005, P = 0.0015; P = 0.0018, P = 0.0005; P = 0.0014, P = 0.0006; P = 0.0025, P = 0.0012). Following western blot analysis also revealed that upregulation of miR-26a/miR-26b could repress cell metastasis and cell cycle (Fig. 2i–j. P = 0.0011, P = 0.0003, P = 0.0003, P = 0.0006, P = 0.0007, P = 0.0016; P = 0.0004, P = 0.0009, P = 0.0024, P = 0.0007, P = 0.0005, P = 0.0011).
Overexpression of miR-26a and miR-26b enhanced TSCC cell apoptosis, but repressed glycolysis
To investigate the effect of miR-26a and miR-26b on cell apoptosis of TSCC cells, flow cytometry analysis was conducted. As exhibited in Fig. 3a, b, gain of both miR-26a and miR-26b distinctly elevated the apoptotic rate of transfected SCC4 and Cal27 cells, leading to about threefold augment (P = 0.0006, P = 0.0002; P = 0.0002, P = 0.0007). In addition, western blot assay was applied to clarify the effect of miR-26a and miR-26b on the protein levels of two apoptosis related proteins, Bax and Bcl-2, in treated cells. The results indicated that upregulated miR-26a and miR-26b conspicuously elevated Bax expression, while reduced Bcl-2 expression in transfected SCC4 and Cal27 cells (Fig. 3c, d. P = 0.0004, P = 0.0002, P = 0.0008, P = 0.0003; P = 0.0003, P = 0.0009, P = 0.0008, P = 0.0007). In addition, both the glucose consumption and lactate production in SCC4 and Cal27 cells with enriched miR-26a and miR-26b expression were lower than that in cells transfected miR-NC, about a half (Fig. 3e–h. P = 0.0006, P = 0.0014; P = 0.0003, P = 0.0006; P = 0.0006, P = 0.0011, P = 0.0003, P = 0.0012).
Both miR-26a and miR-26b targeted PAK1
To explore the underlying mechanism of miR-26a and miR-26b in TSCC cells, bioinformatics analysis was employed to seek out the potential target mRNAs of miR-26a and miR-26b, and indicated that PAK1 contained two common potential binding sites for miR-26a and miR-26b (Fig. 4a, b). To validate the prediction, we transfected 293T cells with PAK1-WT or PAK1-MUT, together with miR-26a or miR-26b. The dual-luciferase reporter assay suggested that overexpression of both miR-26a and miR-26b caused a notable reduction of luciferase activity (approximately 60%) in 293T cells treated with PAK1-WT1 or PAK1-WT2, but not in those treated with PAK1-MUT1 or PAK1-MUT2 (Fig. 4c, d. P = 0.0007, P = 0.0005). To further confirm the predicted interaction between miR-26a/miR-26b and PAK1, RIP assay was also performed. As shown in Fig. 4e, f, upregulation of miR-26a or miR-26b triggered the copious enrichment of PAK1 in Ago2 immunoprecipitation complex, suggesting the target interaction between miR-26a/miR-26b and PAK1 (P = 0.0002, P = 0.0002; P = 0.0001, P = 0.0001).
PAK1 was highly expressed in TSCC tissues and cell lines, and was negatively regulated by miR-26a/miR-26b
RT-qPCR assay demonstrated that PAK1 expression was notably elevated in 44 TSCC tissues and 4 TSCC cell lines compared with corresponding controls (Fig. 5a, b. P < 0.0001; P < 0.0001, P < 0.0001, P = 0.0144, P = 0.0023). SCC4 and Cal27 cells with miR-26a/miR-26b overexpression or inhibition were constructed to analyze the effect of miR-26a/miR-26b on PAK1 expression. Western blot assay revealed that upregulation of miR-26a/miR-26b evidently inhibited the protein level of PAK1, while downregulation of miR-26a/miR-26b induced opposite effect (Fig. 5c, d. P = 0.0021, P = 0.001, P = 0.0004, P = 0.0007; P = 0.0003, P = 0.0013, P = 0.0004, P = 0.002).
Introduction of PAK1 partially reversed overexpressed miR-26a/miR-26b-mediated suppression of cell cycle, migration and invasion in TSCC cells
To explore the regulatory effects of PAK1 upon the functional roles of miR-26a/miR-26b in TSCC progression, rescue experiments were performed in SCC4 and Cal27 cells by transfecting with miR-NC, miR-26a/miR-26b mimic, miR-26a/miR-26b mimic + pcDNA Vector or miR-26a/miR-26b mimic + pcDNA-PAK1. Flow cytometry analysis proved that SCC4 and Cal27 cells transfected with miR-26a/miR-26b mimic showed an evident decline of the cell cycle compared with miR-NC-transfected cells, which was effectively overturned by upregulated PAK1 (Fig. 6a–d. P = 0.0046, P = 0.0085, P = 0.0035, P = 0.0041; P = 0.0067, P = 0.004, P = 0.0042, P = 0.0057; P = 0.0034, P = 0.0068, P = 0.0029, P = 0.0034; P = 0.0071, P = 0.0152, P = 0.0036, P = 0.0063). Transwell assay revealed that gain of both miR-26a and miR-26b remarkably repressed the migrated and invasive abilities of SCC4 and Cal27 cells, while accompanied upregulation of PAK1 conspicuously abolished the repressive effect of the migrated and invasive abilities of SCC4 and Cal27 cells induced by miR-26a and miR-26b (Fig. 6e–l. P = 0.0014, P = 0.0022; P = 0.0009, P = 0.0049; P = 0.0006, P = 0.0053; P = 0.0007, P = 0.0033; P = 0.0006, P = 0.0077; P = 0.0007, P = 0.0029; P = 0.0005, P = 0.0038; P = 0.0011, P = 0.0017). As shown in Fig. 6m–p, western blot analysis suggested that introduction of PAK1 almost reversed the miR-26a/miR-26b-induced the reduction in the protein levels of MMP9, CCND1 and PCNA in SCC4 and Cal27 cells (P = 0.0014, P = 0.0031, P = 0.0004, P = 0.0073, P = 0.0032, P = 0.0041; P = 0.0114, P = 0.0028, P = 0.0025, P = 0.0147, P = 0.0003, P = 0.0028; P = 0.001, P = 0.0048, P = 0.0007, P = 0.0034, P = 0.0018, P = 0.0041; P = 0.0041, P = 0.0099, P = 0.0009, P = 0.0022, P = 0.001, P = 0.0033). Therefore, these data demonstrated that introduction of PAK1 partially reverted the suppression of cell cycle, migration and invasion in TSCC cells induced by miR-26a and miR-26b. In other words, miR-26a/miR-26b repressed TSCC proliferation and metastasis by downregulating PAK1.
Upregulation of PAK1 weakened promotion of apoptosis and inhibition of glycolysis induced by miR-26a and miR-26b in TSCC cells
Next, we performed rescue experiments to clarify whether PAK1 could reverse the augment of apoptosis and reduction of glycolysis in TSCC cells triggered by miR-26a/miR-26b. Flow cytometry analysis manifested that upregulated miR-26a and miR-26b contributed to cell apoptosis of SCC4 and Cal27 cells, while reintroduction of PAK1 partially abrogated the impact of miR-26a/miR-26b (Fig. 7a–d. P = 0.0003, P = 0.0017; P = 0.0004, P = 0.0019; P = 0.0002, P = 0.0046; P = 0.0004, P = 0.0018). In addition, increased expression of miR-26a and miR-26b elevated Bax expression but blocked Bcl-2 expression, which was significantly reversed by co-transfection with pcDNA-PAK1 (Fig. 7e–h. P = 0.0005, P = 0.0013, P = 0.0007, P = 0.0015; P = 0.0007, P = 0.0028, P = 0.001, P = 0.003; P = 0.0006, P = 0.0042, P = 0.0004, P = 0.0032; P = 0.0002, P = 0.0037, P = 0.0002, P = 0.0024). As for glycolysis, gain of miR-26a/miR-26b effectively retarded glucose consumption and lactate production of SCC4 and Cal27 cells, but simultaneous introduction of PAK1 abated the inhibitory influence (Fig. 8a–h. P = 0.0003, P = 0.0034; P = 0.0028, P = 0.0034; P = 0.0003, P = 0.0019; P = 0.0021, P = 0.0031; P = 0.0005, P = 0.0047; P = 0.0006, P = 0.0023; P = 0.0009, P = 0.005, P = 0.0013, P = 0.0049). Hence, above outcomes suggested that upregulated PAK1 overturned elevation of apoptosis and reduction of glycolysis induced by miR-26a and miR-26b in TSCC cells, indicating that miR-26a/miR-26b exerted promoted effect on cell apoptosis and inhibitory effect on glycolysis by targeting PAK1.
Upregulation of miR-26a/miR-26b blocked TSCC tumor growth in vivo
Later, we evaluated the function roles of miR-26a/miR-26b, we established nude mice model via injecting SCC4 cells stably expressing miR-NC, miR-26a and miR-26b. We found that miR-26a/miR-26b overexpression triggered approximately 45% reduction of the volume and weight of formed tumor relative to mice in miR-NC group (Fig. 9a–d. P < 0.0001; P < 0.0001; P < 0.0001; P < 0.0001).
In the current study, we observed low-level expression of miR-26a/miR-26b in TSCC tumor tissues and four TSCC cell lines. Overexpressed miR-26a/miR-26b inhibited cell cycle, migration, invasion and glycolysis but promoted apoptosis of SCC4 and Cal27 cells in vitro and hindered tumor growth in vivo. PAK1 was conformed as the common target of miR-26a and miR-26b. Furthermore, rescue experiments suggested that miR-26a/miR-26b exerted their tumor-suppression functions via targeting PAK1.
Emerging evidence have confirmed the important function of microRNAs in cancer development and tumorigenesis, including TSCC, acting as potent oncogenes or tumor suppressors . Dysregulated microRNAs are also involved in the diagnosis and cure of TSCC . In our study, we validated that miR-26a/miR-26b was downregulated in TSCC tumor tissues and cells, which was similar to former reports [11, 12]. The downregulation of miR-26a has been reported in various human malignancies, such as osteosarcoma (OS) , bladder cancer , breast cancer . Liu and his colleagues revealed that miR-26a abundance was frequently decreased in OS tissues and cells, and miR-26a restrained the mobility of OS cells through targeting high-mobility group A1 (HMGA1) . Zhao et al. found that miR-26a may be related to human breast carcinogenesis, which restrains tumor cell proliferation by targeting HMGA1 . In addition, miR-26b was downregulated in locally advanced and inflammatory breast cancer  and non-small-cell lung cancer , functioning as tumor suppressor. To sum up, miR-26a/miR-26b might serve as tumor suppressed factors in TSCC.
TSCC cells with miR-26a/miR-26b overexpression were constructed through transient transfection to study the role of miR-26a/miR-26b in the celluar behaviors, including cell cycle, migration, invasion, apoptosis and glycolysis. Jia et al. pointed out that introduction of miR-26a caused the inhibition on cell proliferation, as well as promotion on cell apoptosis of TSCC cells (SCC-15 and CAL27 cells) . Yang et al. demonstrated that miR-26a/miR-26b hampered colorectal cancer cell aggressiveness via regulating FUT4 expression . A former study performed by Xu et al. indicated that overexpressed miR-26a effectively impeded multiple myeloma cell growth and delayed tumor growth in vivo through regulating CDK6 enrichment . Moreover, miR-26b level was proved to be reduced in TSCC and hindered proliferation and metastasis in TSCC cells through targeting COX-2 . Du and his partners disclosed that miR-26b exerted its tumor suppressive role through the modulation of glycolytic metabolism in OS cells, showing as regulating expression of glycolytic components, LDHA and GLUT-1 . By analyzing pathway of variant expressed protein, miR-26b is the upstream of the glycolysis/TCA cycle and cytoskeletal modulation via Rho GTPases, implying its significance in the breast cancer progression . Analogously, we manifested that introduction of miR-26a or miR-26b restrained cell cycle, migration, invasion and glycolysis, while facilitated apoptosis of SCC4 and Cal27 cells. Additionally, xenograft tumor assay uncovered the tumor suppressor role of miR-26a/miR-26b in vivo, causing smaller tumor size and weight.
Here, we took effort to explore other potential mechanism of miR-26a/miR-26b. Bioinformatic analysis, dual-luciferase reporter assay as well as RIP assay were conducted to seek the downstream gene of miR-26a/miR-26b, and identified PAK1 as a target. Also, PAK1 enrichment was upregulated in TSCC tumor tissues and cell lines in contrast to corresponding negative controls, as expected.
PAK1, a prototype of group I PAKs, was known to function in the key steps of human cancer progression; and its roles were well studied in multiple malignancies, including breast cancer, colon cancer, lung cancer, melanoma, prostate cancer, ovarian cancer and TSCC [30, 31]. For instance, PAK1 was demonstrated to be a target of miR-7 to participate in regulating the proliferation and metastasis of thyroid cancer cells . Furthermore, PAK1, a target gene of miR-494, functioned as an oncogenic factor in breast cancer via activating MAPK signaling pathway and remodeling cytoskeletal . In non-small cell lung cancer (NSCLC), PAK1 served as clinical biomarker and its level was elevated in NSCLC tissues and cells; also, overexpressed PAK1 reverted the inhibitory impact of miR-98 on growth and mobility of NSCLC cells . Parvathy et al. claimed that PAK1 played a significant part in remodeling cytoskeletal, thus influencing the motility and aggressiveness of oral squamous cell carcinoma cells . LncRNA MALAT1/miRNA-140-5p/PAK1 axis modulated the proliferative and mobility abilities of TSCC cells . In our study, rescue experiments were performed and gain of PAK1 partially overturned the upregulation of miR-26a and miR-26b-mediated suppression of cell cycle, migration, invasion and glycolysis, as well as elevation of apoptosis, indicating that miR-26a/miR-26b regulated cell cycle, metastasis, apoptosis and glycolysis in TSCC cells via downregulating PAK1.
There still exist some limitations in our project. For example, based on the ceRNA hypothesis, circRNAs could repress expression levels of their target miRNAs, so as to alter the expression and function of mRNAs , which urging us to search the upstream circRNAs for better understanding of TSCC progression. Moreover, NF-κB pathway was recognized as an important signal pathway involved in the occurrence and development of various human tumors, including TSCC . We would investigate the impact of miR-26a/miR-26b on the activation of this signal pathway.
Taken together, our study proved that miR-26a/miR-26b was apparently downregulated, while PAK1 was highly expressed in TSCC tissues and cells. Moreover, gain of miR-26a or miR-26b blocked cell cycle, migration, invasion and glycolysis but promoted apoptosis by inhibiting PAK1 in vitro. Overexpression of miR-26a/miR-26b also inhibited TSCC tumor propagation in vivo. Above outcomes disclosed that miR-26a/miR-26b acted as tumor suppressor and might function as therapeutic target of TSCC patients.
Availability of data and materials
The analyzed data sets generated during the present study are available from the corresponding author on reasonable request.
Tongue squamous cell carcinoma
p21 Activated Kinase 1
Reverse transcription-quantitative polymerase chain reaction
Normal human oral keratinocyte
Dulbecco’s Modified Eagle Medium
Fetal bovine serum
Matrix metalloproteinase 9
Proliferating Cell Nuclear Antigen
B cell lymphoma-2
Sodium dodecyl sulphate–polyacrylamide gel electrophoresis
High-mobility group A1
Non-small cell lung cancer
Zheng X, et al. MicroRNA-24 induces cisplatin resistance by targeting PTEN in human tongue squamous cell carcinoma. Oral Oncol. 2015;51(11):998–1003.
Gu Y, et al. miR-22/KAT6B axis is a chemotherapeutic determiner via regulation of PI3k-Akt-NF-kB pathway in tongue squamous cell carcinoma. J Exp Clin Cancer Res. 2018;37(1):164.
Chen W, et al. Cancer statistics in China, 2015. CA Cancer J Clin. 2016;66(2):115–32.
Ma L, et al. Long noncoding RNA GIHCG enhanced tongue squamous cell carcinoma progression through regulating miR-429. J Cell Biochem. 2018;119(11):9064–71.
Bartel DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004;116(2):281–97.
Di Leva G, et al. MicroRNAs in cancer. Annu Rev Pathol. 2014;9:287–314.
Li D, et al. miR-19a and miR-424 target TGFBR3 to promote epithelial-to-mesenchymal transition and migration of tongue squamous cell carcinoma cells. Cell Adhes Migr. 2018;12(3):236–46.
Wu X, et al. MicroRNA-802 plays a tumour suppressive role in tongue squamous cell carcinoma through directly targeting MAP2K4. Cell Prolifer. 2017;50(3):e12336.
Zhu Y, et al. MicroRNA-26a/b and their host genes cooperate to inhibit the G1/S transition by activating the pRb protein. Nucleic Acids Res. 2012;40(10):4615–25.
Chen J, et al. MiRNA-26a contributes to the acquisition of malignant behaviors of doctaxel-resistant lung adenocarcinoma cells through targeting EZH2. Cell Physiol Biochem. 2017;41(2):583–97.
Cao J, et al. miR-26b is downregulated in human tongue squamous cell carcinoma and regulates cell proliferation and metastasis through a COX-2-dependent mechanism. Oncol Rep. 2015;33(2):974–80.
Jia LF, et al. Expression, regulation and roles of miR-26a and MEG3 in tongue squamous cell carcinoma. Int J Cancer. 2014;135(10):2282–93.
Kumar R, et al. p21-activated kinases in cancer. Nat Rev Cancer. 2006;6(6):459–71.
Ye DZ, et al. PAK signaling in cancer. Cell Logist. 2012;2(2):105–16.
Yue K, et al. microRNA-7 regulates cell growth, migration and invasion via direct targeting of PAK1 in thyroid cancer. Mol Med Rep. 2016;14(3):2127–34.
Liang J, et al. Numb inhibits cell proliferation, invasion, and epithelial-mesenchymal transition through PAK1/beta-catenin signaling pathway in ovarian cancer. Onco Targets Ther. 2019;12:3223–33.
Kou B, et al. miR-145 inhibits invasion of bladder cancer cells by targeting PAK1. Urol Oncol. 2014;32(6):846–54.
Zhu M, et al. lncRNA MALAT1 potentiates the progression of tongue squamous cell carcinoma through regulating miR-140-5p-PAK1 pathway. Onco Targets Ther. 2019;12:1365–77.
Karatas OF, et al. MicroRNAs in human tongue squamous cell carcinoma: from pathogenesis to therapeutic implications. Oral Oncol. 2017;67:124–30.
Yu X, et al. MicroRNA expression and its implications for diagnosis and therapy of tongue squamous cell carcinoma. J Cell Mol Med. 2016;20(1):10–6.
Liu J, et al. miR-26a suppresses osteosarcoma migration and invasion by directly targeting HMGA1. Oncol Lett. 2018;15(6):8303–10.
Lin Y, et al. miR-26a inhibits proliferation and motility in bladder cancer by targeting HMGA1. FEBS Lett. 2013;587(15):2467–73.
Zhao XX, et al. MicroRNA-26a inhibits proliferation by targeting high mobility group AT-hook 1 in breast cancer. Int J Clin Exp Pathol. 2015;8(1):368–73.
Ding Q, et al. Decreased expression of microRNA-26b in locally advanced and inflammatory breast cancer. Hum Pathol. 2018;77:121–9.
Jiang LP, et al. Expression of miRNA-26b in the diagnosis and prognosis of patients with non-small-cell lung cancer. Future Oncol. 2016;12(9):1105–15.
Li Y, et al. Tumor-suppressive miR-26a and miR-26b inhibit cell aggressiveness by regulating FUT4 in colorectal cancer. Cell Death Dis. 2017;8(6):e2892.
Xu YY, et al. MicroRNA-26a inhibits multiple myeloma cell growth by suppressing cyclin-dependent kinase 6 expression. Kaohsiung J Med Sci. 2019;35(5):277–83.
Du JY, et al. miR-26b inhibits proliferation, migration, invasion and apoptosis induction via the downregulation of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase-3 driven glycolysis in osteosarcoma cells. Oncol Rep. 2015;33(4):1890–8.
Verghese ET, et al. MiR-26b is down-regulated in carcinoma-associated fibroblasts from ER-positive breast cancers leading to enhanced cell migration and invasion. J Pathol. 2013;231(3):388–99.
Parvathy M, et al. Potential role of p21 Activated Kinase 1 (PAK1) in the invasion and motility of oral cancer cells. BMC Cancer. 2016;16(Suppl 1):293.
Lin XJ, et al. hsa-miR-485-5p reverses epithelial to mesenchymal transition and promotes cisplatin-induced cell death by targeting PAK1 in oral tongue squamous cell carcinoma. Int J Mol Med. 2017;40(1):83–9.
Zhan MN, et al. MicroRNA-494 inhibits breast cancer progression by directly targeting PAK1. Cell Death Dis. 2017;8(1):e2529.
Yang G, et al. MiR-98 inhibits cell proliferation and invasion of non-small cell carcinoma lung cancer by targeting PAK1. Int J Clin Exp Med. 2015;8(11):20135–45.
Shang Q, et al. The novel roles of circRNAs in human cancer. Mol Cancer. 2019;18(1):6.
Chen W, et al. Odd-skipped related transcription factor 1 (OSR1) suppresses tongue squamous cell carcinoma migration and invasion through inhibiting NF-κB pathway. Eur J Pharmacol. 2018;839:33–9.
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Expression of miR-26a/miR-26b in head and neck squamous cell carcinomas. Analyzation of miR-26a/miR-26b expression in head and neck squamous cell carcinomas using YM500v (a, b) and starBase 3.0 (c, d).
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Wei, Z., Chang, K., Fan, C. et al. MiR-26a/miR-26b represses tongue squamous cell carcinoma progression by targeting PAK1. Cancer Cell Int 20, 82 (2020). https://doi.org/10.1186/s12935-020-1166-6