Introduction
Recently, the incidence of thyroid cancer has increased significantly, and its incidence is increasing faster than that of many other malignancies [1, 2]. In China, there are over ninety thousand new thyroid cancer cases every year [3]. Differentiated thyroid carcinoma (DTC) accounts for approximately 90% of all thyroid cancers, and papillary thyroid carcinoma (PTC) is the most prevalent subtype [4]. There is a higher likelihood of lymph node metastasis for early PTC than for other types [5], and because the symptoms of PTC are nonspecific, lymph node metastasis often occurs before diagnosis and is the main reason underlying the progression and recurrence of PTC; moreover, this event consider worsens patients’ quality of life and prognosis [6]. Therefore, early identification of PTC lymph node metastasis can help reduce the recurrence rate and improve patient prognosis.
Long noncoding RNAs (lncRNAs), noncoding RNAs (ncRNAs) ranging in length from 200 to 100,000 nucleotides and are usually located in the nucleus and cytoplasm [7]. LncRNAs may play a key role in cancer development by regulating chromatin remodelling [8], transcription [9], RNA degradation [10], translation regulation [11], and other pathways. Currently, multiple studies have found that lncRNAs have a significant effect on tumour progression and lymph node metastasis [12, 13], including PTC [14, 15]. LINC00894 overexpression was found to exhibit a close association with the proliferative and invasive abilities of kidney and lung cancers [16, 17]. In breast cancer, LINC00894 enhances breast cancer proliferative and invasive capabilities via competitive binding with miR-429 [18]. These studies suggest that dysregulation of LINC00894 contributes to tumour progression, and its function varies with tumour type. Nevertheless, the precise mechanism underlying the involvement of LINC00894 in PTC progression and lymph node metastasis remains unclear.
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M6A modification, the most common RNA modification, is catalysed by a multicomponent methyltransferase complex, and the methyltransferase METTL3 is involved in the formation of m6A as its catalytic core [19, 20]. METTL3 was shown to be involved in tumour progression, such as promoting the progression of colon cancer through tumour immunosuppression [21], mediating acetylation to promote the progression of breast cancer [22], and regulating the m6A modification level of mRNA to facilitate the progression of bladder cancer [23]. The promotion of cancer in the majority of tumours is associated with the upregulation of METTL3 expression; however, the mechanism underlying its role is different. Its latent function in PTC and the mechanism by which METTL3 inhibits the aggressive phenotype of PTC are still unclear.
In this study, a comprehensive analysis of public databases and tissue microarrays was conducted to identify lncRNAs with differential expression between normal thyroid tissue, PTC, and PTC with lymph node metastases. The results indicated a significant progressive decrease in LINC00894 expression these three tissue types. According to the study, LINC00894 in thyroid cancer has a close correlation with lymph node metastasis and a poor prognosis. We then identified the biological function of LINC00894, and the results of functional experiments revealed that LINC00894 overexpression caused significant inhibition of cell proliferation and lymphatic metastasis in vitro. Furthermore, we identified LINC00894 as a probable direct target modulated by the METTL3-YTHDC2 axis and confirmed that LINC00894 exerts its biological effect by modulating the Hippo signalling pathway. These findings highlight new molecular mechanisms for thyroid cancer development and new treatment approaches.
Materials and methods
Analysis of public databases
Datasets for this study are available in the Gene Expression Omnibus (GEO) database or in the Cancer Genome Atlas (TCGA) database. 30 normal thyroid tissues, 33 PTC tissues without lymphatic metastasis, and 23 PTC tissues with lymphatic metastasis were included in this study from the public dataset. Level-three expression data obtained using RNA sequencing, together with the corresponding clinical data for PTC patients, were obtained from the TCGA dataset, accessible at (https://portal.gdc.com). The GTEx datasets, specifically the V8 version, were acquired via the official GTEx data portal website (https://www.gtexportal.org/home/datasets).
Cell lines and cell culture
The Nthy-ori3-1 cell line, representing thyroid follicular epithelial cells, and three PTC cell lines (KTC-1, BCPAP, TPC-1) were procured from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). Additionally, human umbilical vein endothelial cells (HUVECs) were procured from American Type Culture Collection (Manassas, VA, USA). The cell culture was maintained in RPMI-1640 medium (Gibco, Grand Island, NY, USA) that contained 1% penicillin/streptomycin and 10% foetal bovine serum (FBS). Subsequently, the cell lines were subjected to incubation at 37 °C and 5% CO2 [24].
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Cell transfection
The following constructs were procured from RiboBio Co. (Guangzhou, China): pcDNA empty vector, pcDNA-LINC00894, pcDNA-METTL3, pcDNA-YTHDC2, siRNA normal control (SI-NC), and siRNAs targeting LINC00894 (SI-LINC00894). The process of transfection was carried out utilizing either Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) or X-tremeGENE transfection reagent (Thermo Fisher Scientific, USA) following the manufacturer’s protocols [25].
RNA extraction, reverse transcription, and real-time PCR
TRIzol reagent (Invitrogen, Carlsbad, CA, USA) was utilized to isolate total RNA from the cells following the manufacturer’s protocols. Subsequently, 1 µg RNA was subjected to reverse transcription with a Qiagen kit (Qiagen, Valencia, CA, USA) to obtain cDNA. The resulting cDNA was subjected to qRT‒PCR utilizing the SYBR Premix Ex Taq Kit (Takara, Otsu, Japan) on the StepOnePlus™ Real-Time PCR System (Applied Biosystems; Shanghai, China). The 2−ΔΔCt method was utilized to quantify relative expression, with GAPDH serving as the endogenous control [26]. The primer sequences were as follows:
LINC00894: forward: 5′-CCAAATCTGACACACCATAGC-3′;
reverse: 5′-GAACACAGCATGCAGGTAAT-3′.
GAPDH: forward: 5′-GCTGTAGCCAAATCGTTGT-3′,
reverse: 5′-CCAGGTGGTCTCCTCTGA-3′.
METTL3: forward: 5′-AAGCTGCACTTCAGACGAAT-3′,
reverse: 5′-GGAATCACCTCCGACACTC-3′.
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YTHDC2: forward: 5′-CAAAACATGCTGTTAGGAGCCT-3′,
reverse: 5′- CCACTTGTCTTGCTCATTTCCC-3′.
Subcellular RNA fractionation
Nuclear and cytoplasmic RNA was extracted using the NE-PER Nuclear and Cytoplasmic Extraction Kit (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s protocol. Briefly, approximately 10 × 104 cells were suspended in 300 µl of fractionation buffer and then centrifuged at 4°C to isolate the cytoplasmic fraction. The nuclear pellet was then fragmented with cell disruption buffer, and the same volume of 2X lysis/conjugation solution as the RNA lysate was added to the nuclear lysis product, which was finally treated with 100% ethanol. qRT‒PCR was performed to detect the relative RNA levels in the nucleus and cytoplasm. U6 was used as a positive nuclear control, and GAPDH was used as a cytoplasmic control [25, 26].
Fluorescence in situ hybridization
PTC cells were inoculated in 24-well plates, and when the cells grew to a suitable density, the medium was discarded and the cells were washed with PBS. Subsequently, the cells were fixed with 4% PFA paraformaldehyde, washed and added with prehybridization solution at 65 °C for 1 h. Then the hybridization solution containing the probe was added and reacted in the dark at 65 °C in a hybridizer for 48 h. The cells were washed with 4× and 2× SSC, and then subjected to DAPI staining. The slices were observed by fluorescence microscopy after sealed [27]. RNA FISH probes were designed and synthesized by Ribobio (Guangzhou, China).
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Tube formation assay
Precooled Matrigel was added to a 96-well plate and subjected to incubation at 37 °C for 30 min. HUVECs (2 × 104 cells/well) were suspended in 200 µL of conditioned medium and subsequently transferred to the corresponding well and incubated with supernatants from specified KTC-1 and BCPAP cells in 5% CO2 at 37 °C for 8–12 h [28]. The images of tube structures were detected under an inverted bright-field microscope at 100× magnification, and photographs were taken. ImageJ software was used to determine the number of meshes.
Cell counting Kit-8 (CCK-8) assay
Cell viability was assessed through CCK-8 assays [29]. KTC-1 and BCPAP cells were resuspended and subsequently seeded into 96-well plates with a total of five wells allocated to each group. Every well was filled with 2 × 103 cells and 100 µL of medium, which was then subjected to incubation at 37 °C with 5% CO2 for 0, 1, 2, 3, 4, and 5 consecutive days. The 10 µL CCK-8 solution (KeyGEN, Nanjing, China) was pipetted into each well, followed by a 2-hour incubation period. The cellular proliferation rate was measured at 450 nm absorbance through an enzymatic marker.
5-Ethynyl-2′-deoxyuridine incorporation assay
Cell proliferation was assessed using the 5-ethynyl-2′-deoxyuridine (EdU) assay kit (RiboBio) according to the manufacturer’s guidelines [26, 29‐31]. Tumour cells were inoculated into 96-well plates(2 × 104 cells/well ) 24 h after transfection. After 18–24 h of cell culture, the cells were treated with 50 µM EdU for 2 h at 37 °C, fixed with 4% paraformaldehyde, incubated with 2 mg/mL glycine for 5 min, incubated with PBS containing 0.5% Triton X-100 for 10 min, dipped in 1× Apollo staining solution and finally incubated with 100 ml of 1× Hoechst 33,342 for 30 min. The percentage of EdU-positive cells was detected by fluorescence microscopy.
Colony formation assay
A colony formation assay was utilized to evaluate the colony formation ability of cells. PTC cells were inoculated into 6-well plates (100 cells/well) and then cultured at 37 °C and 5% CO2 for 14 days, and the medium was replaced every 3–5 days on a regular basis. After 14 days, the medium was removed, and the cells were fixed with paraformaldehyde. Afterwards, the cells were subjected to staining with 0.1% crystal violet, followed by a 20-min incubation at room temperature (RT). Colonies were counted and photographed [29].
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MeRIP-qPCR
The Magna meRIP M6A Kit (Millipore, Germany) was utilized to conduct the meRIP assay for the purpose of determining m6A enrichment following the manufacturer’s protocols. The PTC cells were subjected to lysis using complete RIP lysis buffer, following which the total RNA was extracted. The RNA samples were subjected to immunoprecipitation with magnetic beads containing either anti-m6A antibody or anti-mouse IgG. The RNAs that were coprecipitated went through a purification process and were subsequently dissolved in RNAse-free water. qRT‒PCR was used to analyse m6A enrichment of binding RNA targets.
Western blotting analysis
The PTC cells were subjected to protein extraction through RIPA buffer (Beyotime Biotechnology, Shanghai, China) containing protease and phosphatase inhibitors (Merck, Germany). After separating the proteins using SDS‒PAGE, they were transferred onto a polyvinylidene difluoride (PVDF) membrane. The membrane was then blocked for 60 min with QuickBlock™ Western Blocking Buffer (P0252, Beyotime Biotechnology, Shanghai, China) and subjected to incubation overnight at 4 °C. After five washes with TBST for 5 min, the secondary antibody combined with horseradish peroxidase (HRP) was applied for incubation at RT for one hour, and the protein was detected with BeyoECL Moon reagent (Beyotime Biotechnology, Shanghai, China).
Statistical analysis
Statistical analysis was conducted by SPSS 19.0 software (IBM, Chicago, USA) and GraphPad Prism 8 (San Diego, USA). The study employed one-way analysis of variance (ANOVA) for determining the significance of differences between multiple groups, while Student’s t test was utilized to evaluate the significance of differences between two groups. The data are reported as the mean ± standard deviation (SD). p < 0.05 was considered to indicate a significant difference.
Results
Low LINC00894 expression is significantly correlated with a poor prognosis and lymphatic metastasis in thyroid cancer patients
To identify lncRNAs strongly associated with PTC, publicly available datasets from the TCGA and GEO were downloaded for bioinformatics analysis (Fig. 1A). Subsequently, lncRNAs differentially expressed in normal thyroid tissue and PTC tissue without lymphatic metastasis, PTC tissue without lymphatic metastasis, and PTC tissue with lymphatic metastasis in the GSE60542 dataset were screened out, and LINC00894 was finally selected as the target lncRNA (Fig. 1B). Further experiments and database analysis demonstrated that the expression of LINC00894 was lower in PTC without lymphatic metastases than in normal thyroid tissue, and LINC00894 was lower in PTC with lymph node metastases than in PTC without lymph node metastases (Fig. 1C-G). According to qRT-PCR data, LINC00894 expression was downregulated in PTC cells compared to that in normal cells (Fig. 1H). Survival analysis suggested that patients with low LINC00894 expression had significantly lower overall survival rates (Fig. 1I). The findings indicate that low LINC00894 expression is related to PTC progression and lymphatic metastasis.
Fig. 1
Decreased Expression of LINC00894 in PTC Tissues and Cells. (A) Relative LINC00894 expression in normal thyroid tissue, PTC tissue without lymphatic metastasis, and PTC tissue with lymphatic metastasis using GEO (GSE60542). (B) Venn diagram showing the overlapping differentially expressed lncRNAs, depending on A1 and A2. (C) Assessment of LINC00894 expression in normal thyroid tissue, PTC tissue without lymphatic metastasis, and PTC tissue with lymphatic metastasis (PTC-LNM) using TCGA data. (D) Assessment of LINC00894 expression in normal thyroid tissue using the Genotype-Tissue Expression (GTEx) database. (E) Assessment of LINC00894 expression in normal and tumour tissues using the Gene Expression Profiling Interactive Analysis (GEPIA) database. (F) Assessment of LINC00894 expression in THCA based on TCGA data. (G) Assessment of LINC00894 expression in THCA using GEPIA data. (H) QRT-PCR analysis of LINC00894 expression levels in PTC cell lines. (I) Analysis of the clinical impacts of abnormal LINC00894 expression on PTC patient overall survival using Kaplan‒Meier Plotter. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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LINC00894 overexpression inhibits lymphangiogenesis and PTC cell proliferation in vitro
To analyse the impact of LINC00894 on the functional phenotype of PTC cells, we first predicted the low coding potential of LINC00894 using CPC2 (http://cpc2.gao-lab.org/index.php) (Fig. 2A). Bioinformatics was also applied to predict the cellular distribution of LINC00894 in various cells, and it was found to be mainly located in the cytoplasm (Fig. 2B). Subsequently, subcellular fractionation and FISH assays were performed in PTC cells. Our results showed that it was more highly expressed in the cytoplasm than in the nucleus (Fig. 2C-D), consistent with the predicted results. Subsequently, the LINC00894 overexpression plasmid was transfected into KTC-1 and BCPAP cells, and the overexpression efficiency of LINC00894 was verified (Fig. 2E). We found that the medium from LINC00894-overexpressing PTC cells inhibited mesh formation by cells (Fig. 2F-H). Colony formation, EdU and CCK-8 assays confirmed that LINC00894 overexpression significantly inhibited PTC cell proliferation (Fig. 2I-O).
Fig. 2
LINC00894 inhibits the lymphangiogenesis of vascular endothelial cells and the proliferation of PTC cells. (A) Predicting the coding capability of LINC00894 using the CPC2 database. (B) Bioinformatics analyses predicted the subcellular distribution of LINC00894 in various cells. (C) Subcellular localization of LINC00894 in KTC-1 and BCPAP cells. The nuclear marker was U6, and the cytosol marker was GAPDH. (D) FISH analysis of the location of LINC00894 in the cytoplasm and nuclear fractions of PTC cells. (E) Verification of the overexpression efficiency of LINC00894 through qRT‒PCR. F and H. Effect of altered LINC00894 expression in PTC cells on HUVEC tube formation. I and K. For LINC00894-overexpressing cells, a colony formation assay was used to evaluate PTC cell proliferation. L and M. For LINC00894-overexpressing cells, the CCK-8 assay was used to evaluate PTC cell viability. N and O. For LINC00894-overexpressing cells, the EdU assay was used to evaluate cell proliferations. **P < 0.01, ***P < 0.001, ****P < 0.0001
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METTL3 expression is closely correlated with LINC00894 expression in PTC
Given the significant impact of m6A modification on gene expression regulation in malignancies, we conducted SRAMP analysis (http://www.cuilab.cn/sramp/), and the results revealed that a large number of m6A modification sites exist in LINC00894 (Fig. 3A). Since m6A modifications are added or removed by a series of methylases or demethylases, such as METTL3, METTL14, METTL16, ALKBH5, FTO, and others [32, 33], to identify the specific genes that lead to changes in m6A modification, we analysed the correlation between related genes and LINC00894 through the StarBase database (https://starbase.sysu.edu.cn/) (Fig. 3B). Subsequently, the expression of relevant enzymes in PTC tissues and normal thyroid tissues was analysed using the GEPIA database (http://gepia.cancer-pku.cn/); the results revealed that METTL3 was significantly downregulated in PTC tissues vs. normal thyroid tissues, and there was no significant difference for other enzymes (Fig. 3C). We further demonstrated that METTL3 was downregulated in PTC through the TCGA database (Fig. 3D). Survival analysis suggested that patients with low levels of METTL3 had significantly lower overall survival rates (Fig. 3E). Subsequently, METTL3 overexpression was found to promote LINC00894 expression in PTC cells (Fig. 3F). The abovementioned results indicate that METTL3 is significantly downregulated in PTC and may influence the expression of LINC00894 through m6A modification.
Fig. 3
METTL3 is closely associated with the expression of LINC00894 in PTC. (A) Prediction of m6A sites of LINC00894 using the SRAMP database. (B) Analysis of the correlation between methylases or demethylases and LINC00894 using the starBase database. (C) Assessment of methylase or demethylase expression in THCA using GEPIA data. (D) Assessment of METTL3 expression in THCA based on TCGA data. (E) Assessment of the clinical impacts of abnormal METTL3 expression on PTC patient overall survival using Kaplan‒Meier Plotter. (F) Detection of LINC00894 expression following METTL3 overexpression using qRT‒PCR. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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METTL3 enhances LINC00894 mRNA stability through the M6A-YTHDC2-dependent pathway
To validate the potential impact of METTL3-mediated m6A modification on LINC00894, we conducted meRIP-PCR analysis, which indicated that the m6A level of LINC00894 increased significantly after METTL3 was upregulated (Fig. 4A). As expected, METTL3 overexpression enhanced the stability of LINC00894 mRNA (Fig. 4B-C). Although m6A modification is performed by RNA methyltransferases, m6A-modified RNAs can selectively bind to different m6A readers, resulting in different modifications [34]. We used annonlnc (http://annolnc.gao-lab.org/index.php) to find that LINC00894 has high-affinity binding sites for YTHDC2 (Fig. 4D). Then, we further demonstrated a positive association between YTHDC2 and LINC00894 levels in THCA and confirmed that YTHDC2 was significantly downregulated in PTC tissues (Fig. 4E-F). More importantly, YTHDC2 overexpression was found to elevate LINC00894 expression in PTC cells (Fig. 4G). Similarly, LINC00894 mRNA stability was enhanced when YTHDC2 was overexpressed (Fig. 4H-I). In summary, these findings suggest that METTL3 enhances LINC00894 mRNA stability through the m6A-YTHDC2-dependent pathway.
Fig. 4
METTL3 enhances LINC00894 mRNA stability through the M6A-YTHDC2-dependent pathway. A. Enrichment of METTL3-mediated LINC00894 m6A modification using meRIP-qPCR. B-C. Detection of LINC00894 expression in actinomycin D-treated PTC cells overexpressing METTL3 using qRT‒PCR. D. Displaying the binding site of YTHDC2 and LINC00894 using the AnnoLnc2 database. E. Analysis of the correlation between YTHDC2 and LINC00894 using the starBase database. F. Detection of LINC00894 expression using qRT‒PCR following YTHDC2 overexpression. H-I. Detection of LINC00894 expression levels in actinomycin D-treated PTC cells overexpressing YTHDC2 using qRT‒PCR. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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Reversal of the tumour-suppressive effects of METTL3 by silencing LINC00894
To verify whether METTL3 contributes to the suppressive effects of PTC through LINC00894, we designed siRNA targeting LINC00894. Rescue experiments showed that by using METTL3-overexpressing PTC cells, HUVECs formed fewer meshes, while the inhibitory effects could be reversed by LINC00894 siRNA (Fig. 5A-C). According to the colony formation and CCK-8 assays, METTL3 overexpression also suppressed the proliferative abilities of PTC cells, and these effects could be reversed by LINC00894 siRNA transfection (Fig. 5D-H).
Fig. 5
Reversal of the Tumour-Suppressive Effects of METTL3 by Silencing LINC00894. Functional rescue experiments, including the tube formation assay of HUVECs (A-C), colony-forming assays (D-F), and CCK-8 assays (G-H), were performed. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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LINC00894 inhibits PTC malignant phenotypes through the Hippo signalling pathway
LncRNAs have been reported to be involved in tumours via various signalling pathways [35]. To explore the signalling pathway downstream of LINC00894, we first examined the differentially expressed genes (DEGs) in normal thyroid tissues and PTC tissues using the TCGA database (Fig. 6A-B). Subsequently, the RNA-seq data were analysed via the Kyoto Encyclopedia of Genes and Genomes (KEGG); the Hippo signalling pathway exhibited significant enrichment in the low LINC00894 expression group in comparison to the high LINC00894 expression group (Fig. 6C). Further analysis revealed that LINC00894 and METTL3 were significantly positive correlated with key components of the Hippo pathway (TAZ, YAP, LATS1, and MST1) (Fig. 6D-E). Then, Western blotting was used to examine LINC00894’s effect on related proteins in this pathway, revealing that after LINC00894 overexpression, YAP and TAZ protein expression decreased significantly, while the expression of ECA protein increased (Fig. 6F). Based on these findings, we deduced that LINC00894 may inhibit PTC malignant phenotypes via Hippo signalling.
Fig. 6
LINC00894 inhibits PTC malignant phenotypes through the Hippo signalling pathway. A-B. TCGA analysis was performed to identify differentially expressed genes in normal thyroid tissue and PTC tissue. C. KEGG pathway enrichment analysis. D. Analysis of the correlation between LINC00894 and TAZ, YAP, LATS1, and MST1 using the starBase database. E. Analysis of the correlation between METTL3 and TAZ, YAP, LATS1, and MST1 using the starBase database. F. Protein expression levels of Hippo signalling pathway-related proteins after pcDNA-LINC00894 transfection in KTC-1 cells according to Western blotting. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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Discussion
Thyroid cancer has a high prevalence, and most cases are PTC, which is the most common endocrine malignancy [4]. Approximately 40% of adult PTC patients also have lymph node metastasis, which is correlated with higher recurrence rates and lower survival rates [36, 37]. Ultrasound, CT, and FDG-PET/CT have low sensitivity for the detection of lymph nodes positive for lateral and intercentral compartment tumours [38, 39]. There are only three main treatment options for differentiated thyroid cancer: surgical resection, TSH inhibition and radioactive iodine therapies; however, the lymph node metastasis rate within 20 years of unilateral thyroid lobotomy with DTC is 19%, and secondary surgery is the only option for patients at this time [40]. However, the heterogeneity among the histological and epigenetic characteristics of PTC is not well understood. Therefore, the identification or discovery of novel molecular markers in patients with PTC may improve the detection of metastatic lymph nodes and better guide treatment.
Multiple studies have revealed that lncRNAs are dysregulated in cancers with lymph node metastasis, and lncRNAs can exist in serum, plasma, or other body fluids in a stable form without being affected by endogenous RNA enzymes [41, 42], which makes lncRNAs a potential tumour marker for a variety of tumours [43]. LINC00894 contributes to the progression of various tumours, and the proliferative and invasive capabilities of kidney and lung cancer are closely related to its overexpression [16, 17]. In breast cancer, LINC00894 enhances breast cancer cell proliferation and invasion by competitively binding with miR-429 [18]. Nevertheless, studies on thyroid cancer have found that upregulation of LINC00894 can inhibit tumour cell activity [25]. LINC00894 has not yet been evaluated for its clinical significance and function in lymph node metastatic PTC. Herein, by using bioinformatics, LINC00894 expression was found to be significantly lower in PTC with lymph node metastasis than in PTC without lymph node metastasis, and the prognosis was worse when LINC00894 expression was lower. Functional tests indicated that LINC00894 overexpression significantly suppressed cell proliferation and lymphatic metastasis in vitro, whereas silencing LINC00894 induced the opposite effects. Based on these findings, we first elucidated the critical role of LINC00894 in the lymphatic metastasis of PTC.
Until now, no investigations have been conducted on the regulatory mechanism mediated by abnormal LINC00894 expression. Given the significant function of m6A modification in the regulation of gene expression in tumours, we further explored whether the downregulation of LINC00894 in PTC is related to m6A. By epigenetic transcriptomic analysis, we found that LINC00894 has a large number of methylation sites, and the m6A level is significantly positively correlated with METTL3 expression. It was confirmed that METTL3-induced m6A modification increased the stability of LINC00894 mRNA. The literature reports that METTL3 exhibits dual functionality as an oncogene and tumour suppressor [44]. METTL3 was reported to be downregulated in PTC and to suppress epithelial-mesenchymal transformation and Hedgehog signalling [29]. This is consistent with our findings. METTL3 is the main methyltransferase, and m6A readers, such as YTHDFs and IGF2BPs, recognize and act on m6A-modified mRNA transcripts [45, 46]. Further studies showed that overexpression of METTL3 and YTHDC2 significantly stabilized and promoted LINC00894 mRNA expression. The aforementioned findings suggested that METTL3 increases LINC00894 mRNA stability through the M6A-YTHDC2-dependent pathway. In recent years, targeting METTL3 to alleviate cancer progression has attracted much attention. Research has indicated that elvitegravir has the ability to suppress oesophageal cancer metastasis by increasing the proteasome degradation of the M6A methyltransferase METTL3 [47]. Our findings on the METTL3-LINC00894 axis, as well as its effect on PTC progression, will aid in the exploration of more effective treatment strategies for lymphatic metastasis of PTC.
Several signalling pathways have been demonstrated to participate in tumour inhibition or promotion by lncRNAs [48]. By KEGG enrichment analysis, the Hippo signalling pathway was indicated to be significantly enriched in PTC tissues with low LINC00894 expression. This signalling pathway regulates tissue growth, was first discovered in Drosophila melanogaster [49] and is highly conserved in humans. Studies in recent decades have revealed that the Hippo signalling pathway is dysfunctional in various malignancies, including liver [33], stomach [50], and lung cancers [51]. Dysregulation of the Hippo signalling pathway was also found in thyroid cancer [52]. In this study, it is innovatively proposed that LINC00894 regulates the Hippo signalling to affect PTC progression. This may be used as a potential therapeutic target for PTC treatment. However, the specific mechanism of this crosstalk remains to be determined, especially at the molecular level.
In conclusion, these results suggest that the METTL3-YTHDC2 axis regulates the stability of LINC00894 mRNA in an m6A-dependent manner and subsequently inhibits tumour malignancy through the Hippo signalling pathway.
Acknowledgements
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Declarations
All study participants provided informed consent, and the study design was approved by an ethics review board. This manuscript has not been published and is not under consideration for publication elsewhere. All the authors have approved the manuscript and agree with this submission. All the authors declare no competing interests.
Ethics approval and consent to participate
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Consent for publication
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Competing interests
The authors declare no competing interests.
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