Background
Oral squamous cell carcinoma (OSCC) ranks the sixth most common malignancies around the world, with a relatively lower five-year survival rate of approximate 50% [
1]. Recent epidemiological data showed that high-risk human papillomaviruses (HPVs), particularly HPV-16, have emerged as an additional causative agent of OSCC besides excessive tobacco and alcohol consumption [
2]. HPV-positive OSCC defines a novel and independent entity with distinct genetic nature and clinicopathological features when compared to HPV-negative OSCC, while treatment approaches towards them are essentially the same which depend on the site and stage of the tumor [
3]. Even though patients with HPV-positive OSCC show better prognosis [
4], they are typically associated with positive lymph nodes, and current treatments still fail to cure more than a quarter of them with advanced stages [
5‐
7]. Therefore, there is an urgent need to study the molecular mechanisms responsible for invasive phenotype and progressive potentials of HPV-positive OSCC.
Migration and invasion of tumor cells into surrounding microvasculature of the lymphatic system, are crucial steps of the lymphatic dissemination of malignant tumors [
8]. During these processes, the so-called epithelial-mesenchymal transition (EMT) is taken place with increased mesenchymal markers such as Vimentin and N-cadherin, and decreased epithelial markers such as E-cadherin and β-catenin [
9]. At present, emerging studies have reported that tumor-associated macrophages (TAMs), which are derived from peripheral blood monocytes and the most abundant among tumor-infiltrating immune cells, exert critical functions in tumor metastasis via modulating EMT [
10]. Stimulated by various secreted factors in tumor microenvironment, M1 or M2 macrophages can be polarized from TAMs. M1 macrophages exhibit pro-inflammatory roles and promote immune response to prevent oncogenic impacts, while M2 macrophages are important for pro-tumorigenic processes, and stimulation of tumor angiogenesis, cancer progression, immunosuppression, and matrix remodeling [
11]. In triple-negative breast cancer (TNBC), cancer cells-derived IL-6 could stimulate M2 macrophages polarization, which promoted EMT and invasiveness of TNBC cells [
12]. In addition, Li and colleagues have reported that hepatocellular carcinoma-conditioned TAMs possessed M2-like phenotype, and could contribute to the EMT and invasion in hepatocellular carcinoma [
13]. Conversely, in a study of breast cancer, not only TAMs could induce EMT, but mesenchymal-like cancer cells could in turn activate more macrophages recruitment by secreting GM-CSF and promote cancer metastasis [
14]. Although evidence has shown that HPV-positive OSCC exhibited enhanced immune activity with respect to HPV-negative OSCC [
15], the crosstalk between the intrinsic mechanisms of cancer cells and the extrinsic microenvironmental factors such as TAMs that influence EMT and progression of HPV-positive OSCC remains unclear.
microRNAs (miRNAs) include a class of endogenous, noncoding small RNAs (19–24 nucleotides), which serve as post-transcriptional gene regulators to impact comprehensive biological processes [
16]. Multiple studies have uncovered that miRNAs have crucial roles in the development and progression of human cancers, exerting their effects by affecting the intrinsic mechanisms, or communicating with extrinsic properties [
17,
18]. However, while deregulated miRNAs have already been detected in HPV-positive OSCC [
19,
20], the underlying mechanisms of whether miRNAs could orchestrate HPV-positive OSCC progression remain limited. Here, we speculated that miRNAs could mediate the crosstalk between cancer cells and TAMs to regulate malignant behaviors of HPV-positive OSCC.
In the present study, we clarified that decreased miR-550a-3-5p expression was correlated with HPV-positive OSCC metastasis. Functional experiments identified that miR-550a-3-5p inhibited M2 macrophages polarization, which in turn suppressed migration, invasion and EMT of HPV-positive OSCC cells. Furthermore, mechanistic studies revealed that miR-550a-3-5p, reduced by E6 oncoprotein, inhibited M2 macrophages polarization by regulating YAP/CCL2 axis, the correlation of which was confirmed in both xenografts of nude mice and clinical specimens. These findings improved our knowledge of the molecular mechanisms by which miRNA regulated HPV-positive OSCC progression, and provided possible therapeutic target for HPV-positive OSCC.
Methods
Patients and clinical specimens
Seventy primary OSCC tissue specimens between 2015 and 2016 were collected from patients with informed consent at West China Hospital of Stomatology, Sichuan University. All of these patients have undergone the curative resection and were devoid of prior treatment or autoimmune diseases. Specimens were identified as squamous cell carcinoma and classified into different grades based on the current Union for International Cancer Control (UICC) criteria. Besides, 20 normal oral mucosa were obtained and all tissues samples were half frozen for RNA and DNA extraction, and half fixed in 10% formalin and embedded in paraffin. The current study was authorized by the Institutional Ethics Committee of the West China Medical Center, Sichuan University, China.
HPV detection
Total DNA was extracted using DNA Extraction Kit (Tiangen) according to manufacturer’s instructions. HPV status was determined using a highly sensitive PCR protocol (Invitrogen) and HPV-16/18 primers, which was performed on a C1000 Touch PCR machine (Bio-Rad). Specific primers for HPV16: forward, 5′-CACAGTTATGCACAGAGCTGC-3′, reverse, 5′-CATATATTCATGCAATGTAGGTGTA-3′; HPV-18: forward, 5′-CACTTCACTGCAAGACATAGA-3′, reverse, 5′-GTTGTGAAATCGTCGTTTTTCA-3′. Then, eletrophoresis with 1.5% agarose gels was used to separate PCR products, which were visualized by GCLSTAIN staining.
miRNA microarray
An Agilent miRNA microarray (8*60 K, Design ID: 070156) using clinical specimens from HPV-positive and HPV-negative OSCC patients was carried out to profile miRNA by oeBiotech Limited Company. Total RNA was extracted using TRIzol reagent (Invitrogen) following manufacturer’s protocols and 100 ng RNA per sample was used in microarray.
qRT-PCR
Total RNA was extracted as previously defined. For mature miRNAs, All-in-One™ miRNA First-Strand cDNA Synthesis Kit (Genecopoeia) was used to generate 10 μL cDNA. Then using miR-specific primers and universal adaptor PCR primers (Genecopoeia), qRT-PCR was performed with All-in-One™ miRNA qRT-PCR Detection Kit (Genecopoeia) on CFX Connect Real-Time System (Bio-Rad). For mRNA, the reverse transcription was carried out using HiScript II Q RT SuperMix (Vazyme), and qRT-PCR was performed with ChamQ™ SYBR Color qPCR Master Mix (Vazyme) on CFX Connect Real-Time System (Bio-Rad) [
21]. Specific primers for qRT-PCR of mRNA were listed in
Supplementary Data. The U6 small nuclear RNA or GAPDH was used as an endogenous control. Each experiment was repeated at least three times and the results were analyzed using 2
-△△CT method.
Western blot
The whole proteins were extracted using cell lysis buffer. Then, SDS-PAGE was used to separate proteins with different sizes. After that, protein was transferred to a PVDF membrane (Millipore) and target protein was immunoblotted with specific primary antibody. Primary antibodies were listed as follows: anti-E-cadherin (1:5000, mouse anti-human, Cell Signaling Technology Inc.), anti-Vimentin (1:2000, mouse anti-human, Abcam), anti-HPV16 E6 + HPV18 E6 (1:1000, mouse anti-human papillomavirus, Abcam), anti-HPV16 E7 (1:1000, mouse anti-human papillomavirus, Abcam), anti-YAP (1:2000, mouse anti-human, Proteintech), anti-TAZ (1:2000, mouse anti-human, Proteintech), anti-CCL2 (1:2000, mouse anti-human, Proteintech), anti-flag-YAP (1:1000, mouse, Abbkine), anti-GAPDH (1:2000, rabbit anti-human, Sigma-Aldrich). After incubating goat anti-rabbit or goat anti-mouse secondary antibody (MultiSciences), immunoblots were visualized using the chemiluminescence (ECL) reagent (Beyotime Biotechnology) and ChemiDoc XRS+ System (Bio-Rad).
miRNA fluorescence in situ hybridization (FISH)
FISH assays were performed using miRNA Fluorescence In Situ Hybridization Kit (GenePharma) according to the instructions. Oligonucleotide modified probe labeled with cy3 for hsa-miR-550a-3-5p was provided by GenePharma. First, 5 μm formalin-fixed paraffin-embedded sections were preheated for 30 min at 60 °C and fresh xylene was used to remove paraffin from the tissue. Then, sections were rehydrated by 5 min incubations in decreasing concentrations of ethanol, and incubated with Proteinase K solution for 15 min at 37 °C and denaturing solution for 8 min at 78 °C. After dehydration, probes were added in the hybridization solution and incubated for 4 h at 50 °C. Sections were washed and counterstained with DAPI (GenePharma). Images were acquired using a fluorescence microscope (Olympus BX51).
Immunohistochemistry (IHC)
Formalin-fixed paraffin-embedded sections were firstly deparaffinized using xylene and rehydrated in alcohol with decreasing concentrations. Then boiling for 3 min in 0.01 M citrate buffer (pH = 6.0) was used for antigen retrieval, and 3% hydrogen peroxide was added for blocking endogenous peroxidase activity. After that, we used 5% goat serum for antigen blocking and incubated sections with the primary antibody at 4 °C overnight in a moist chamber. Sections were washed with PBS, and incubated first with biotinylated anti-mouse/rabbit IgG and sequent with streptavidin-biotin peroxidase both for 15 min. DAB was added to detect the primary antibody, and hematoxylin was used to stain the nucleus. As negative controls, sections were analyzed in parallel except incubating with isotype-specific immunoglobulin (IgG) instead of the primary antibody. And the following primary antibodies were listed: anti-p16 for detecting p16, a surrogate biomarker of HPV E7 oncoprotein function (1:500, rabbit anti-human, Bioss), anti-Ki-67 (1:200, rabbit anti-human, HUABIO), anti-E-cadherin (1:500, mouse anti-human, Cell Signaling Technology Inc.), anti-Vimentin (1:200, mouse anti-human, Abcam), anti-CD31 (1:300, rabbit anti-human, Biorbyt), anti-CD34 (1:300, mouse anti-human, HUABIO), anti-YAP (1:600, mouse anti-human, Proteintech), anti-CCL2 (1:200, mouse anti-human, Proteintech), anti-CD163 (1:500, rabbit anti-human, Biorbyt). HE staining was referred to as hematoxylin and eosin staining. Staining of IHC was evaluated in 10 randomly selected fields at 400X magnification. Quantification was evaluated by three independent investigators who were blinded to patient characteristics. IHC staining scores were calculated as staining intensity × percentage of positive cells. Staining intensity was assigned as: 0 (negative), 1 (weak), 2 (moderate), 3 (strong). Percentage of positive cells was defined as: 0 (no positive cells), 1 (<10% positive cells), 2 (10–50% positive cells), 3 (>50% positive cells). For CD163 staining, positive cells in each field were counted and expressed as the mean value [
22].
Cell culture and reagents
HPV16-positive human OSCC cell lines UPCI:SCC090 and UM-SCC-47, HPV-negative human OSCC cell lines Cal-27, SCC25, and HSC3, normal human oral keratinocytes (NOK), dysplasia human oral keratinocytes (DOK), and human monocyte cell line THP-1 were obtained from State Key Laboratory of Oral Disease, Sichuan University. UPCI:SCC090 and UM-SCC-47 were cultured in MEM (Gibco) containing 1X non-essential amino acids (Sigma-Aldrich), 1 mM sodium pyruvate (Sigma) and 10% fetal bovine serum (FBS, Gibco), Cal-27 and HSC3 were cultured in DMEM (Gibco) containing 10% FBS, SCC25 was cultured in DMEM/F12 (Gibco) containing 10% FBS, NOK and DOK were cultured in EpiLife (Gibco), and THP-1 was cultured in RPMI 1640 medium (Gibco) with 10% FBS. All of them were maintained at 37 °C in a humidified atmosphere with 5% CO2. For macrophage generation, THP-1 cells were induced by 200 nM PMA (Sigma-Aldrich) for 24 h. Then OSCC cells whether transfected or not, were cultured with serum-free medium for 24 h and the supernatant was collected and centrifuged at 1000 x g for 20 min, known as the conditioned media (CM). We obtained tumor-associated macrophages (TAMs) by culturing PMA-induced THP-1 cells in CM of OSCC cells for 24 h. Morphology and polarization of TAMs were observed and detected. Co-cultivation of TAMs and OSCC cells was performed with the non-contact transwell system (pore size 0.4 μm, corning). TAMs seeded in the upper chamber communicated with corresponding OSCC cells in the lower chamber for 48 h, and OSCC cells were harvested for further analysis.
Verteporfin (VP, Selleck) was dissolved in DMSO and used in the culture medium at a final concentration of 10 μM for 24 h. Recombinant human CCL2 (Sino Biological) was added to CM at 500 ng/mL before inducing PMA-THP-1 cells.
Transfections
miR-550a-3-5p mimic or inhibitor were obtained from GenePharma Co. Ltd., China. Small-interfering RNAs (siRNAs) targeting E6, E7, and YAP were designed and synthesized also by GenePharma Co. Ltd., China. The plasmid pCDH-EF1-YAP-5SA (FLAG-tagged) and the empty Vector were kindly provided by Dr. Fanyuan Yu in West China School of Stomatology, Sichuan University and used for overexpression of activated YAP. The plasmid CS-GS3114-Lv201 for HPV16 E6 overexpression (OE) was designed by GenePharma Co. Ltd., China, and EX-NEG-Lv201 was used as the negative control. These transfections were performed using EndoFectin™ (GeneCopoeia) according to the manufacturer’s instructions. Forty-eight hours after transfection, further experiments could be carried out. Stably-transfected OSCC cells with miR-550a-3-5p overexpression were derived from the parental cells by a fluorescence microscope (Olympus BX51) detection and puromycin (Sigma-Aldrich) selection.
Cell proliferation assay and flow cytometry-based apoptosis analysis
CCK-8 assay was used to study cell proliferation. Cells were seeded in 96-well plates at the density of 1 × 103 (cells/well), and the absorbance at 450 nm was measured on 24, 48, 72, 96, 120 h with 10 μL of CCK-8 solution. Proliferative comparison of mimic-transfected cells or inhibitor-transfected cells was calculated by normalization with respect to NC: % cells = (mimic or inhibitor – corresponding NC)/ corresponding NC × 100. Difference of OD Value on 120 h and OD Value on 24 h was used for calculation. Each assay was carried out in triplicate.
Flow cytometry using the Annexin V-FITC Apoptosis Detection Kit (Invitrogen) was used to measure cell apoptosis. Cells were seeded in 6-well plates and digested after 48 h. Then, 1X Binding Buffer was used to resuspend cells. We stained cells with 5 μL of Annexin V-FITC Conjugate and 5 μL of Propidium Iodide Solution and incubated them for 30 min. Stained cells were analyzed using a FACScalibur (Becton-Dickinson). For comparison, % apoptotic cells = (mimic or inhibitor – corresponding NC)/ corresponding NC × 100. Experiments were conducted in triplicate.
Wound healing assay and cell invasion assay
Cells were cultured in 6-well plates and starved in serum-free medium for 24 h after arriving at 100% confluence. A pipette tip was used to scratch the cells and form the gap space. After washing out the dead cells, photomicrographs were taken immediately and at a timepoint of 24 h. Closed scratch areas were calculated by ImageJ software. Each experiment was conducted in triplicate.
24-well transwell plates (pore size 8 μm, Millipore) were used for conducting Cell invasion assays. The upper chamber was coated with Matrigel (BD Bioscience) before 5 × 104 cells being seeded in it. After 24 h of cell adherence, medium was changed into serum-free in upper chamber and complete medium was added to lower chamber. Then, cells which have invaded through the Matrigel after 24 h incubation were stained with 0.1% crystal violet and counted under a microscope. Five pre-selected fields (× 200) were observed and assays were conducted in triplicate.
Imaging of macrophage morphology
Fluorescent staining was used for observation of macrophage morphology. Macrophages were washed with PBS for three times, and fixed with 4% paraformaldehyde for 20 min. Then, PBS containing 0.5% Triton X-100 was used to permeabilize the cells for 5 min. After incubating cells with FITC-phalloidin (Solarbio) for 30 min, nuclei were stained using DAPI (Sigma-Aldrich). All photographs were taken using a fluorescence microscope (Olympus BX51).
Dual luciferase reporter gene assays
The wild-type or mutant YAP 3’UTR pEZX-FR02 plasmids designed by GeneCopoeia Co. Ltd., was cotransfected with miR-550a-3-5p mimic or NC in UPCI:SCC090 and UM-SCC-47 cells using EndoFectin™ (GeneCopoeia). Forty-eight hours after transfection, cell lysates were collected and used for detection of firefly and Renilla luciferase activities following the protocol of a Luc-Pair™ Duo-Luciferase Assay Kit 2.0 (GeneCopoeia). Renilla luciferase activity was used for normalization in the study.
Animal experiments
All animal experiments were approved by the Institutional Animal Care and Use Committee of West China Medical Center, Sichuan University. For subcutaneous xenograft model of nude mice, twenty 4-week-old BALB/c male nude mice (Dashuo) were divided into four groups after 1 week acclimation. Stably miR-550a-3-5p-overexpressed UPCI:SCC090 and Cal-27 cells and their relevant empty vector-transfected control cells were injected into the right flank region of nude mice subcutaneously. 0.2 mL containing 5 × 106 cells per aliquot was used in each mouse. Tumor volumes were evaluated every 3 days and calculated using formula as below: length × (width)2 × ∏/6. Mice were killed using isoflurane after 8 times taking notes of tumor volume, and tumors were collected for weights measuring and further examination.
For 4NQO-indued OSCC model of transgenic mice, a total of sixteen 7-week-old female Rosa26-E6-E7 constitutive knock-in C57BL/6 mice (Cyagen, ID: TOS150814BA1) were used and divided into two groups randomly after 1 week of acclimation: 4NQO + VP group (
n = 8) and 4NQO group (
n = 8). A solution of 4NQO (Sigma-Aldrich) was added to the distilled drinking water at a concentration of 100 μg/mL for 8 weeks, and then switched to distilled water for another 8 weeks to generate OSCC as we previously described [
23]. After that, VP (Selleck) was injected every 3 days intraperitoneally at 100 mg/kg in 4NQO + VP group, while Vehicle-treated mice were injected with DMSO. Mice were anesthetized using isoflurane after 6 doses of VP, and tongue was collected, carefully observated and longitudinally bisected. We fixed one part of each tongue tissue with 10% formalin and embedded it with paraffin, and froze the other part immediately and stored it at − 80 °C.
Statistical analysis
The correlations between miR-550a-3-5p expression and other clinicopathlogical factors were estimated using Chi-square analysis. The overall survival was assessed using the Kaplan-Meier method, and statistical significance between groups was estimated by log-rank test. Means comparisons were conducted with Student t-test or one-way ANOVA. The associations between miR-550a-3-5p and YAP, YAP and CCL2, and CCL2 and CD163 expressions in HPV-positive OSCC specimens were assessed using 2-tailed Pearson’s statistics. All cellular experiments were conducted independently for at least three times and in triplicate each time. GraphPad Prism 7.0 (GraphPad Software) was used for processing all data and values were presented as means ± SD. P<0.05 was considered to be statistically significant.
Discussion
Previous researches have evidently certificated that even though HPV-positive OSCC presents a relatively better prognosis in most cases, it usually exhibits an aggressive behavior with lymph nodes already being metastasized [
37]. Wakisaka et al. have showed that in clinical specimens of OPSCC, HPV positivity was significantly correlated with EMT induction. These EMT-positive cases showed more relevance with advanced nodal status [
38]. Mechanistically, a study has revealed that HPV 16 E7 oncoprotein expression in keratinocytes could epigenetically repress the E-cadherin expression by augmenting cellular DNA methyltransferase I activity [
39]. E5, together with E6 and E7 could impair cell adhesion, and promote migratory and invasive properties via inhibiting E-cadherin expression [
40]. Moreover, there was a study implying that HPV16 E6 and E7 could induce EMT-relevant molecular alterations independently through non-transcriptional ways, thus leading to malignant progression of epithelial cells [
41]. Consistently, our study found that in HPV-positive OSCC cells, the effects of miR-550a-3-5p on suppressing M2 macrophages polarization, and thus migration, invasion and EMT phenotype relied on the regulation of its upstream factor E6 oncoprotein. This described at least in part the mechanisms by which E6 promoted EMT of HPV-positive OSCC.
Continuous expression of the viral E6/E7 oncogenes is required for HPV-positive cancer development [
42]. Mechanistically, E6 promotes the proteolytic degradation of p53 tumor suppressor protein while E7 primarily interferes with the activity of tumor suppressor protein pRb, despite the fact that other molecules also appear to be deregulated due to E6/7 stimulation [
26,
43]. A previous study has reported that E6/7-dependent maintenance of the malignant phenotype of HPV-positive cancer cells is linked to specific changes of intracellular miRNA pool [
44,
45]. However, the specific modulatory mechanisms vary among different miRNAs. For example, Peta and colleagues found that HPV16 E6 and E7 could repress miR-146a-5p expression at the promoter level through elevating transcription factor c-MYC [
46]. In addition, HPV16 E6 could inhibit miR-22 expression, and thus suppress proliferation, migration and induce apoptosis of cervical cancer cells by down-regulating p53, a direct transcriptional regulator of miR-22 [
47]. Meanwhile, HPV16 E6/p53 also reduces miR-34a expression transcriptionally, therefore leading to increased glycolysis in cervical cancer [
48]. In our study, miR-550a-3-5p expression and its subsequent inhibitory effects on M2 macrophages polarization were negatively regulated by E6 oncoprotein, while the specific mechanisms remain unknown and need further investigation.
Lots of previous studies only concentrated on the intrinsic mechanisms of miRNAs in cancer cells, however, the miRNAs-mediated crosstalks between cancer cells and tumor microenvironment which could also affect cancer metastasis have recently been investigated [
49]. For example, miR-141-3p was able to inhibit normal fibroblasts’ transition to cancer-associated fibroblasts via STAT4/wnt/β-catenin pathway, thus leading to suppressed migration and invasion in gastric cancer cells [
50]. Highly expressed miR-301a-3p, induced by hypoxia in pancreatic cancer cells, could mediate M2 macrophages polarization to promote cancer metastasis via direct exosome delivery [
51]. Also in this study, we found a signaling pathway that influenced tumor microenvironment and was mediated by miR-550a-3-5p, which modulated TAMs polarization and in turn affected migration, invasion, and EMT of HPV-positive OSCC cells.
miR-550 has been reported to be differentially expressed in several types of cancers and exert important regulatory effects on cancer development. In non-small cell lung cancer, Yang and colleagues have showed that miR-550a-3p was highly expressed and promoted proliferation, migration and invasion of cancer cells by targeting TIMP2 [
52]. In colorectal cancer cells, miR-550a-5p was inversely regulated by tumor suppressor Brg-1, and promoted migration and invasion via RNF43/Wnt/β-catenin pathway [
53]. However, due to the tissue specificity, miR-550 also exerts tumor-suppressor roles. For example, down-regulated miR-550a-3p led to the initiation, growth and metastasis of breast cancer by promoting ERK1/2 levels [
54]. The same as above, miR-550a-3-5p was negatively associated with the growth and metastatic potential of both HPV-positive and negative OSCC cells in our study. Down-regulation of miR-550a-3-5p indicated higher tumor size and nodal metastasis of HPV-positive OSCC patients, suggesting its anti-tumor role especially in HPV-positive OSCC. Furthermore, unlike in other types of cancer, though its inhibitory roles in HPV-negative OSCC and in growth of HPV-positive OSCC might derive from direct mechanisms which need further investigation, miR-550a-3-5p affected migration and invasion of HPV-positive OSCC cells indirectly as the discrepancy between in vivo and in vitro studies. Thus, here we aimed to search for the downstream pathways of miR-550a-3-5p and verify whether these molecules resulted in the indirect tumor-suppressive influences of miR-550a-3-5p. Through bioinformatics analysis, gene expression patterns and dual luciferase reporter gene assays, we found that miR-550a-3-5p directly targeted YAP which emerged to exhibit great roles in cancer immunity, and further regulated M2 macrophages polarization and migration, invasion and EMT of HPV-positive OSCC cells via YAP/CCL2 signaling. Similarly, a recent study also reported that miR-550a-3-5p could directly target YAP to exert tumor-suppressor roles in various cancers containing colon cancer, breast cancer, lung cancer, and head and neck cancer [
55]. However, this didn’t include OSCC cell lines and only concentrated on the direct effects of miR-550a-3-5p.
YAP, as a central effector of the Hippo pathway and a transcriptional co-activator with TAZ, takes great part in controlling organ size, development, and tumorigenesis [
56,
57]. Canonically, core kinase cascade of the Hippo pathway Mst1/2-Lats1/2 is responsible for phosphorylation of YAP/TAZ, which then leads to its cytoplasmic retention, ubiquitination and degradation [
58]. However, there are also non-canonical pathways that promote nucleus-translocation of YAP/TAZ, and thus stimulate its transcriptional activities, through which YAP/TAZ plays important tumor-promoting roles in a number of cancers [
59]. Several studies have also showed that aberrant YAP accumulation in the nucleus of cancer cells was found in both cervical cancer and HPV-positive OSCC, and HPV-positive patients with higher YAP levels usually had a more advanced stage [
60‐
62]. Moreover, Webb Strickland and colleagues have reported that E6 oncoprotein could associate with cellular PDZ domain proteins to promote the nuclear localization of YAP [
63]. In our study, we put forward a pathway in which miR-550a-3-5p, down-regulated by E6 oncoprotein, inhibited YAP but not TAZ in HPV-positive OSCC. Then, we found that YAP inhibition could suppress cancer progression using YAP inhibitor Verteporfin in 4NQO-induced OSCC model of E6-E7 knock-in mice. These results were consistent with the relatively high expression of YAP and its tumor-promoting role in HPV-positive cancers.
The transcriptional activities of YAP/TAZ are mainly conducted by binding to the TEAD family and thus promoting the expression of genes critical for cancer cell proliferation, survival and stemness [
64]. We have detected its classical target genes including CTGF, CYR61, CCNE2, CDC6 and CDK2 in our study, and only CCNE2 and CDC6 were up-regulated in YAP-activated HPV-positive OSCC cells, while miR-550a-3-5p overexpression could weaken these effects. These may partly explain the mechanism by which miR-550a-3-5p regulated proliferation and apoptosis of cancer cells. However, no significant changes were observed in expressions of other canonical target genes, which may ascribe to the different context in HPV-positive OSCC, according to a recent article studying the molecular signature regulated by YAP/TAZ in OSCC cells [
34]. Recently, accumulating evidence suggests that the effect of YAP is not confined to cancer cells, but instead involves the regulation of cancer immune microenvironment. Secretion of certain cytokines or chemokines by cancer cells could be modulated owing to increased YAP activity, thus recruiting myeloid-derived suppressive cell (MDSCs) or M2 macrophages and inhibiting anti-tumor immunity [
28‐
30]. In line with this, we found that YAP, down-regulated by miR-550a-3-5p, could promote CCL2 expression transcriptionally by interaction with TEAD family, thus contributing to M2 macrophages polarization.
CCL2 is a highly expressed chemokine in cancer cells and secreted to contribute to cancer progression [
65,
66]. In addition, CCL2 also enhances TAMs infiltration and exerts tumor-promoting effects indirectly [
67]. For example, CCL2, which was induced by FoxQ1/VersicanV1 in hepatocellular carcinoma cells, could promote TAMs infiltration and then contribute to cancer progression [
68]. Moreover, CCL2, produced by breast cancer cells, could continually recruit inflammatory monocytes and promote their differentiation into TAMs, which facilitated the subsequent growth of metastatic cells [
69]. Our results revealed that E6/miR-550a-3-5p/YAP could promote M2 macrophages polarization through increasing CCL2, thus leading to the enhanced EMT in HPV-positive OSCC cells. As shown in Fig.
7e, findings of our studies were summarized in a schematic.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.