LINC00238 inhibits hepatic carcinoma progression by activating TMEM106C‑mediated apoptosis pathway
- Authors:
- Published online on: September 2, 2021 https://doi.org/10.3892/mmr.2021.12397
- Article Number: 757
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Copyright: © Jiang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Hepatocellular carcinoma (HCC) is the fourth major cause of cancer mortality worldwide and the global morbidity of the disease is increasing (1). Surgical resection is the most effective treatment method of all therapy methods; however, most patients are initially diagnosed as advanced and untreatable by surgery (2). High rates of postoperative recurrence and metastasis are also reasons for the high mortality rate of HCC (3). Although great progress in the therapy methods has been made in the last few decades, the survival rate of patients with HCC remains poor (4). Hence, the search for new effective therapeutic targets is of great significance for HCC treatment.
In recent years, an increasing numbers of studies have focused on the effect of lncRNAs on the occurrence and development of HCC (5–7). Research has shown that aberrant expression of long non-coding RNAs (lncRNAs) decelerates or accelerates the progression of HCC. For instance, a study by Liu et al (8) demonstrates that lncRNA Ftx can inhibit proliferation and metastasis of HCC and that higher lncRNA Ftx expression is associated with longer survival. Furthermore, long intergenic non-protein coding (LINC)RNA-p21 overexpression reduces the levels of epithelial-mesenchymal transition (EMT)-related proteins and decrease tumor metastasis in HCC (7). The findings of Wang et al (9) indicate that high lncRNA ATB expression promotes proliferation of HCC and is positively correlated with poorer survival of patients with HCC. Gong et al (6) found that LINC00238 is expressed at low levels in HCC samples. However, the regulatory mechanism of LINC00238 in HCC remains to be elucidated.
The transmembrane protein (TMEM) family is a class of proteins containing one or more putative transmembrane segments that span partially or completely through biological membranes (10). As a member of the TMEM family, TMEM106 is involved in several diseases, including cancer. In a study on non-small cell lung carcinoma, Liu and Zhu (11) found that TMEM106A is an anti-oncogene that inhibits the proliferation and invasion of lung cancer cells. Lang et al (12) note that abnormal expression of TMEM106B is associated with progression of frontotemporal lobar degeneration. In addition, Assassi et al (13) found that TMEM106C is aberrantly expressed in ankylosing spondylitis. Luo et al (14) have indicate that TMEM106C is involved in HCC development. However, remains to be elucidated whether lncRNAs are involved in the regulation of TMEM106C in HCC progression.
The present study explored the regulatory role of LINC00238 in HCC progression. The findings suggested that LINC00238 expression was decreased in HCC tissues and cell lines and the low LINC00238 expression was associated with the poor prognosis of patients with HCC. LINC00238 inhibited HCC progression by regulating the TMEM106C-mediated apoptosis signaling pathway. Furthermore, ATF3, the gene enriched in the apoptosis pathway, could regulate LINC00238 expression, consequently preventing HCC development.
Materials and methods
Bioinformatics analysis
The online platform Gene Expression Profiling Interactive Analysis (GEPIA) (15) was used to analyze the differentially expressed lncRNAs in HCC. A total of 369 HCC cases and 160 normal were downloaded from The Cancer Genome Atlas (TCGA) database (https://portal.gdc.cancer.gov/). The expression of LINC00238, TMEM106C and ATF3 in HCC tumor tissues and normal tissues were analyzed based on the downloaded data. The overall survival information in this study was downloaded from TCGA database. Survival analysis was performed with the R package ‘survival’ (16,17) by using the Kaplan-Meier curve method and TANRIC platform. The binding sites between LINC00238 and TMEM106C were predicted by LncTar (www.cuilab.cn/lnctar). Gene Set Enrichment Analysis (GSEA) (18) was performed using three gene set datasets [GO-BP (http://www.geneontology.org), KEGG (http://www.genome.jp/kegg/) and Hallmark gene sets (19)] to analyze the impact of TMEM106C on signaling pathways. The JASPAR (http:///jaspar.genereg.net/) and PROMO (alggen.lsi.upc.es/cgi-bin/promo_v3/promo/promoinit.cgi?dirDB=TF_8.3) databases were used to analyze the upstream transcription factor of LINC00238.
Patients and samples
A total of 43 human HCC tissues and corresponding normal tissues were collected from 22 male (age range, 32–64 years) and 21 female (age range, 34–70 years) patients with HCC between January 2018 and September 2019. None of the patients received any treatment before surgical resection, including surgery, radiotherapy and chemotherapy. The study was approved by the ethics committee of Qingdao No. 6 People's Hospital [approval no. (2018) 26] and written informed consent was obtained from all patients.
Cell lines and culture
The human normal hepatic cell line MIHA and HCC cell lines Huh7, HLF, SNU-449, MHCC-97h and HCCLM3 were purchased from Mlbio and cultured in DMEM (Gibco; Thermo Fisher Scientific, Inc.) containing antibiotics (Gibco; Thermo Fisher Scientific, Inc.) and 10% FBS (Gibco; Thermo Fisher Scientific, Inc.), in a humidified atmosphere containing 5% CO2 at 37°C.
Cell transfection
LINC00238-overexpressing plasmid pcDNA3.1 (pc-LINC00238), negative control plasmid (pc-NC), short interfering (si)RNAs targeting LINC00238 (30 nM, si-LINC00238#1, 5′-GAGGATACTTAGGAGAGCTAT-3′; si-LINC00238#2, 5′-GGAGAGCTATGTATCCTATTT-3′; and si-LINC00238#3, 5′-GGCTGGAAGTGTTCAGTTAGT-3′) and negative control siRNA (30 nM, si-NC, 5′-GAGGTATGGTATTCGGTCTGA-3′), TMEM106C-overexpressing plasmid pcDNA3.1 (pc-TMEM106C) negative control plasmid (pc-NC), siRNAs targeting ATF3 (30 nM, si-ATF3#1, 5′-GAGCAGTTCGGTGCATATGGT-3′; si-ATF3#2, 5′-GGGTTACTGGCAGGTTGAACT-3′; and si-ATF3#3, 5′-GGGAAACAGTTGAGAGGTTAT-3′) and negative control siRNA (30 nM, si-NC, 5′-GCTTGGAAGGTCGGTCATGTA-3′), ATF3-overexpressing plasmid pcDNA3.1 (pc-ATF3) negative control plasmid (pc-NC) were purchased from Shanghai GenePharma Co., Ltd. The transfection was performed by Lipofectamine® 3000 (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions. The cells were collected after transfection for 48 h.
Reverse transcription-quantitative (RT-q) PCR
Total RNA was extracted from tissues and cells (1×106) using TRIzol reagent (Thermo Fisher Scientific, Inc.). The PrimeScript RT reagent kit (Takara Bio, Inc.) was used to synthesize cDNA. qPCR was carried out using SYBR Premix Ex Taq II kit (Takara Bio, Inc.) according to the manufacturer's protocol. The reaction conditions were as follows: 95°C for 5 min, followed by 40 cycles of 95°C for 15 sec and 60°C for 30 sec. GAPDH was used as the internal control for mRNA expression. Relative gene expression levels were calculated using the 2−ΔΔCq method (20). All experiments were performed in triplicate. The primers used in the study were: LINC00238: 5′-TTTGCAGAGTGGGTGCTAGG-3′ (forward) and 5′-TGCTTCATCTGGCAATGACCT-3′ (reverse); Transmembrane Protein 106C (TMEM106C): 5′-GCCTGTCCAGCCAGATTCAG-3′ (forward) and 5′-TTCCTACAGCCCCCTACTCT-3′ (reverse); activating transcription factor 3 (ATF3): 5′-AGGTTTGCCATCCAGAACAA-3′ (forward) and 5′-AGGCACTCCGTCTTCTCCTT-3′ (reverse); GAPDH: 5′-CTGGGCTACACTGAGCACC-3′ (forward) 5′-AGTGGTCGTTGAGGGCAATG-3′ (reverse).
Cell proliferation assay
HCC cells were trypsinized and seeded into 96-well culture plates (4,000 cells/well). The cells were harvested at 24, 48, 72 and 96 h to detect proliferation using the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) Cell Proliferation Colorimetric Assay kit (AmyJet Scientific, Inc.) and the absorption was detected at a wavelength of 490 nm.
Cell apoptosis assay
The apoptosis of HCC cells was evaluated using Annexin V/PI apoptosis-detection kit (Invitrogen; Thermo Fisher Scientific, Inc.). HCC cells were washed with Annexin V-binding buffer (Sigma-Aldrich; Merck KGaA), followed by incubation in binding buffer containing Annexin V-FITC (25 µg/ml) and PI (25 µg/ml) in the dark for 10 min at room temperature. Apoptotic cells (early + late apoptotic cells) were analyzed using a BD Accuri C6 Plus flow cytometer and FACSDiva software (version 6.13; BD Biosciences).
Wound healing assay
HCC cells were seeded into 6-well plates and incubated to achieve ≥90% confluence. The monolayer cells were scratched with a 10-µl sterile micropipette tip and cellular debris was removed by washing with PBS. Then, cells were incubated in serum-free medium with proliferation inhibitor mitomycin C (10 µM; MedChemExpress) at 37°C. Cell migration was observed at 0 and 48 h under a light microscope (magnification, ×100, Olympus Corporation) and analyzed with ImageJ version 1.49 software (NIH). All experiments were performed in triplicate.
Transwell assay
The invasion of HCC cells was detected by Transwell assay. The upper chambers (8 µm pore size) were coated with Matrigel at 37°C for 30 min. Cells (1×104 cells/well) were seeded into the upper chamber with serum-free DMEM. DMEM containing 10% FBS was added to the lower chambers. The chambers were incubated for 48 h at 37°C. Subsequently, the noninvasive cells were removed with a cotton swab and the invading cells were fixed with methanol. The cells were then stained with crystal violet at room temperature for 15 min. The number of invasive cells was observed under a light microscope (magnification, ×200; Olympus Corporation).
Western blotting
HCC cells (1×106) were lysed with RIPA buffer (Beyotime, Shanghai, China) to obtain total protein, centrifuged for 10 min at 14,000 × g and the supernatant was collected. The protein concentration was determined using a BCA kit (Beijing Solarbio Science & Technology Co., Ltd.). Subsequently, the proteins (20 µg) were separated by 10% SDS-PAGE and transferred onto PVDF membranes. The membranes were incubated with 5% non-fat dry milk for 1 h at room temperature and then incubated with primary antibodies against TMEM106C (1:500; cat. no. PA5-67816; Thermo Fisher Scientific, Inc.), ATF3 (1:1,000; cat. no. 18665S; Cell Signaling Technology, Inc.), caspase-7 (CASP7) (1:1,000; cat. no. 12827S; Cell Signaling Technology, Inc.), tissue inhibitor of metalloproteinase 2 (TIMP2) (1:1,000; cat. no. 5738S; Cell Signaling Technology, Inc.), programmed cell death 4 (PDCD4) (1:1,000; cat. no. 9535S; Cell Signaling Technology, Inc.) and GAPDH (1:1,000; cat. no. 5174S; Cell Signaling Technology, Inc.) overnight at 4°C, followed by incubation with the Goat anti-Rabbit IgG Secondary Antibody (1:5,000; cat. no. 31466; Thermo Fisher Scientific, Inc.) at room temperature. GAPDH served as the internal reference. The bands were visualized using enhanced chemiluminescence (ECL) detection reagents (Amersham Biosciences; Cytiva). Blots were semi-quantitatively analyzed using ImageJ software (version 2.0; National Institutes of Health).
RNA immunoprecipitation (RIP) assay
To explore the binding relationship between LINC00238 and TMEM106C, the RIP assay was performed using Magna RIP kit (EMD Millipore) according the manufacturer's protocols. HCC cells were lysed with RIPA lysis buffer (EMD Millipore) and then incubated with anti-TMEM106C-coated Dynabeads Protein G (cat. no. PA5-61466; Thermo Fisher Scientific, Inc.) beads at 4°C. IgG (cat. no. ab182931; Abcam) was used as the control. The beads were washed with PBS and incubated with TRIzol (Thermo Fisher Scientific, Inc.) for 30 min at 55°C. The levels of LINC00238 and TMEM106C were measured using RT-qPCR.
Statistical analysis
Data are shown as means ± SD and were analyzed using SPSS 23.0 (IBM Corp.) and GraphPad Prism 7.0 (GraphPad Software, Inc.). Comparisons between two groups were analyzed using unpaired Student's t-test and the comparisons among multiple groups were analyzed by one-way ANOVA followed by Tukey's post hoc test. Pearson's correlation analysis was used to assess the correlation among LINC00238, TMEM106C and ATF3 expression. All experiments were performed in triplicate.
Results
LINC00238 is downregulated in HCC
The online platform GEPIA was used to analyze the differentially expressed lncRNAs in HCC and the results suggested that LINC00238 was downregulated in HCC. The online analysis based on TCGA suggested that LINC00238 levels in HCC tissues were markedly lower compared with those in normal tissues (Fig. 1A) and that LINC00238 levels was positively correlated with the overall survival of patients with HCC (Fig. 1B). LINC00238 expression was measured in HCC tissues and corresponding normal tissues using RT-qPCR. The data showed that LINC00238 was significantly downregulated in HCC tumor tissues (Fig. 1C). High levels of LINC00238 expression were associated with local TNM stage (I/II; Fig. 1D) and non-metastasis (Fig. 1E). LINC00238 expression in human normal hepatic cell line MIHA and HCC cell lines (Huh7, HLF, SNU-449, MHCC-97h and HCCLM3) was measured using RT-qPCR. The results indicated that LINC00238 expression in HCC cell lines was markedly decreased compared with that in the normal hepatic cell line (Fig. 1F). HCCLM3 and MHCC-97h cell lines were selected for further study because of the low LINC00238 expression in these cells.
LINC00238 overexpression inhibits cell proliferation, migration and invasion of HCC cells
The LINC00238 overexpressing plasmid pc-LINC00238 was transfected into HCCLM3 and MHCC-97h cells to detect the influence of LINC00238 on the biological function of HCC cells. As shown in Fig. 2A, LINC00238 expression was significantly increased in the pc-LINC00238 group compared with that in pc-NC group. The proliferation of HCC cells was measured using the MTS assay. The data suggested that LINC00238 overexpression suppressed the proliferation ability of HCCLM3 and MHCC-97h cells (Fig. 2B). Flow cytometry results revealed that the apoptotic rates of HCCLM3 and MHCC-97h cells were significantly increased after LINC00238 overexpression (Fig. 2C). The migration and invasion capacity of HCC cells was detected by wound healing and Transwell assays, respectively. The results in Fig. 2D showed that LINC00238 overexpression markedly decreased the migration capacity of HCC cells. Additionally, the number of invasive cells in the pc-LINC00238 group was significantly reduced compared with that in the pc-NC group (Fig. 2E).
LINC00238 negatively regulates the expression of TMEM106C in HCC
A recent study showed that TMEM106C is highly expressed in HCC and serves an important role in HCC progression (14). LncTar was performed to determine whether there is a targeted relationship between LINC00238 and TMEM106C (21) and the results (Fig. 3A) suggested that TMEM106C was the target gene of LINC00238. The target relationship between LINC00238 and TMEM106C was verified using RIP assay. The data suggested that LINC00238 expression was significantly increased in TMEM106C immunoprecipitates in HCCLM3 and MHCC-97h cells compared with that the Anti-IgG group, suggesting that TMEN106C could couple with LINC00238 directly (Fig. 3B). The protein levels of TMEM106 in HCC cells after LINC00238 overexpression was evaluated using western blotting. The data showed that LINC00238 overexpression significantly reduced TMEM106 expression (Fig. 3C). The online data based on TCGA suggested that TMEM106C is more highly expressed in HCC tumor tissues than in normal tissues (Fig. 3D) and a high level of TMEM106C expression is associated with poor overall survival (Fig. 3E). There was a negative correlation between LINC00238 and TMEM106C expression in HCC (Fig. 3F). TMEM106C expression was detected with RT-qPCR and the correlation between LINC00238 and TMEM106C expression analyzed. The results indicated that TMEM106C expression was significantly upregulated in tumor tissues (Fig. 3G) and negatively correlated with LINC00238 expression (Fig. 3H).
To investigate whether LINC00238 served its role through TMEM106C, pc-LINC00238 and pc-TMEM106C were co-transfected into HCCLM3 and MHCC-97h cells to detect the influence of LINC00238 and TMEM106C on HCC progression. As shown in Fig. 3I, the TMEM106C expression was significantly increased by TMEM106C overexpression. The proliferation ability of HCC cells was markedly enhanced by TMEM106C overexpression (Fig. 3J). Additionally, the capacity of invasion (Fig. 3K) was significantly higher in the p-TMEM106C group than that in the pc-NC group. In addition, the inhibitory effect of LINC00238 overexpression on the proliferation and invasion of HCC cells was eliminated with TMEM106C overexpression.
TMEM106C regulates the apoptosis pathway and LINC00238 is transcriptionally regulated by ATF3 in HCC
The present study performed GESA analysis of the gene sequences of TMEM106C in HCC cells (18). The results showed that TMEM106C suppressed the apoptosis signaling pathway (Fig. 4A). The protein expression of genes enriched in the apoptosis signaling pathway was then detected. Western blot analysis showed that the protein expression of capsase-7 (CASP7), TIMP2, PDCD4 and ATF3 was significantly increased by LINC00238 overexpression and decreased by TMEM106C overexpression (Fig. 4B). The inhibitory effect of TMEM106C on protein expression of ASP7, TIMP2, PDCD4 and ATF3 in HCC cells was eliminated by LINC00238 overexpression (Fig. 4B).
To investigate the potential mechanism of LINC00238 in HCC, the JASPAR and PROMO databases were analyzed and ATF3 was identified as the upstream transcription factor of LINC00238 (Fig. 4C and D). The regulatory effect of ATF3 on LINC00238 expression was detected after ATF3 siRNAs (si-ATF3#1, si-ATF3#2 and si-ATF3#3) were transfected into HCC cells. As shown in Fig. 4E, ATF3 levels were significantly decreased in the si-ATF3 groups. The expression of LINC00238 was markedly suppressed in the si-ATF3 groups compared with that in the si-NC group (Fig. 4F). ATF3 expression in HCC tissues and corresponding normal tissues was measured using RT-qPCR. The results indicated that ATF3 expression in tumor tissues was lower compared with that in normal tissues (Fig. 4G). Online data based on TCGA suggested that ATF3 was expressed at low levels in HCC tumor tissues (Fig. 4H) and low levels of ATF3 expression were associated with poor overall survival (Fig. 4I). Furthermore, there was a positive correlation between ATF3 and LINC00238 and a negative correlation between ATF3 and TMEM106C in HCC (Fig. 4J).
ATF3 overexpression reverses the promoting effect of LINC00238 silencing on HCC progression
The si-LINC00238 and ATF3-overexpressing plasmid were co-transfected into HCC cells to explore the regulatory effect of ATF3 on LINC00238 in HCC progression. As shown in Fig. 5A, LINC00238 expression was significantly decreased by LINC00238 silencing. The ATF3 expression was markedly increased by ATF3 overexpression (Fig. 5B). The MTS data showed that LINC00238 silencing enhanced cell proliferation, whereas ATF3 overexpression reduced the proliferation of HCC cells (Fig. 5C). Compared with the si-LINC00238 group, the proliferation ability of the si-LINC00238+pc-ATF3 group was significantly decreased (Fig. 5C). Apoptosis of HCC cells was measured using flow cytometry. The data suggested that apoptosis of HCC cells was markedly decreased by LINC00238 silencing and increased by ATF3 overexpression (Fig. 5D). The inhibition of LINC00238 silencing on HCC cell apoptosis was eliminated by ATF3 overexpression (Fig. 5D). Additionally, the migration and invasion capacity of HCC cells following co-transfection with si-LINC00238 and pc-ATF3 were measured. The data suggested that the capacity of migration and invasion of HCC cells was significantly enhanced by LINC00238 silencing and reduced by ATF3 overexpression (Fig. 5E and F). Besides, ATF3 overexpression reversed the accelerating effect of LINC00238 silencing on the migration and invasion of HCC cells (Fig. 5E and F).
Discussion
HCC is one of the commonest cancers with high mortality rates worldwide. High rates of metastasis and postoperative recurrence lead to high mortality rate in patients with HCC (3). The present study found that LINC00238 was downregulated in HCC. Overexpression of LINC00238 suppressed proliferation, migration and invasion of HCC cells by activating the TMEM106C-mediated apoptosis signaling pathway. Furthermore, it was found that ATF3, a gene enriched in the apoptosis signaling pathway, was the upstream promoter of LINC00238.
Previous studies have suggested that lncRNAs serve a vital role in the initiation and progression of HCC. Mo et al (22) revealed that LINC01287 expression is increased in HCC cells and knockdown of LINC01287 decreases the proliferation and invasion ability of HCC cells. The lncRNA CTC-297N7.9 acts as a tumor suppressor in HCC and low expression of lncRNA CTC-297N7.9 is associated with poor prognosis in patients with HCC (23). In the present study, the expression of LINC00238 was significantly decreased in both HCC tissues and cell lines. High levels of LINC00238 were associated with a good prognosis. Overexpression of LINC00238 inhibited the proliferation, migration and reduced invasion capacity of HCC cells. These data indicated that LINC00238 acted as a tumor suppressor in HCC and LINC00238 overexpression inhibited HCC progression.
TMEM106C is a member of the TMEM106 family and is expressed at low levels in patients with ankylosing spondylitis (13). Duan et al (24) found that TMEM106C expression is positively related to CENPM and negatively related to DLC-1 in HCC tumor tissues. Luo et al (14) showed that FOXO1 and FOXO3 may be the key target genes of TMEM106C in HCC. In the present study, LINC00238 expression was higher in HCC tissues compared with that in normal tissues. The predicted result of LncTar suggested that TMEM106C was the target of LINC00238. LINC00238 overexpression reduced the protein expression of TMRM106C. TCGA analysis showed that high TMEM106C expression was associated with poor prognosis of HCC and negatively correlated with LINC00238 expression. In addition, TMEM106C overexpression reversed the inhibitory effect of LINC00238 overexpression on the proliferation, migration and invasion of HCC cells. These data suggested that LINC00238 inhibited HCC progression by suppressing TMEM106C expression.
The expression of the ATF3, a member of the ATF family of transcription factors, can be induced by a variety of stress signals (25). Previous studies have demonstrated that ATF3 acts as a tumor inhibitor in cancer. ATF3 dysfunction allows normal cells to be easily transformed by oncogenes (26). For instance, Li et al (27) found that overexpression of ATF3 inhibits the proliferation and migration in esophageal squamous cell carcinoma. The findings of Hackl et al (28) indicated that downregulation of ATF3 promotes the migration capacity of colon cancer cells in vitro and facilitates tumor growth in vivo. Lv et al (29) observed that ATF3 is significantly downregulated in human intrahepatic cholangiocarcinoma with tumor metastasis. The results of the present study were consistent with those of previous studies. The expression of ATF3 was significantly lower in HCC tumor tissues than that in normal tissues. Low ATF3 expression was associated with poor prognosis in patients with HCC. ATF3 overexpression inhibited proliferation, migration and invasion of HCC cells. In addition, it was found that ATF3 was an upstream transcription factor of LINC00238. ATF3 expression was positively correlated to LINC00238 and LINC00238 expression could be reduced by ATF3 silencing. Overexpression of ATF3 reversed the promoting effect of LINC00238 silencing on proliferation, migration and invasion of HCC cells. These results indicated that ATF3 could suppress HCC progression and strengthen the inhibitory effect of LINC00238 on HCC.
Avoidance of apoptosis a major cause of cancer development and progression (30). CASP7 is a member of the caspases family that participates in cervical cancer progression (31). Palmerini et al (32) indicated that CASP7 is downregulated in colon cancer. Proteins encoded by TIMPs are natural inhibitors of matrix metalloproteinases. Peeney et al (33) demonstrated that TIMP2 inhibits the proliferation and EMT progression of triple-negative breast cancer. PDCD4 is a tumor suppressor gene for various cancers and can inhibit cell proliferation, migration and invasion, as well as promote tumor cell apoptosis (34). Hwang et al (35) indicated that overexpression of PDCD4 induces anti-proliferation and apoptosis-induced effects on human lung cancer. In the present study, western blotting data showed that LINC00238 overexpression increased the protein expression of CASP7, TIMP2 and PDCD4. However, the promoting effect of LINC00238 on CASP7, TIMP2 and PDCD4 was eliminated by TMEM106C overexpression. These results suggested that LINC00238 inhibited the proliferation, migration and invasion of HCC cells by upregulating these genes that were enriched in the apoptosis pathway.
In conclusion, LINC00238 was downregulated in HCC tissues and cell lines and served a vital role in restraining HCC progression. Overexpression of LINC00238 decreased TMEM106C expression and increased the expression of CASP7, TIMP2, PDCD4 and ATF3, which are apoptotic pathway genes and thus inhibited the proliferation, migration and invasion of HCC cells. Notably, ATF3 positively regulated the expression of LINC00238, thereby participating in the inhibitory regulation of HCC by LINC00238.
Acknowledgements
Not applicable.
Funding
No funding was received.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Authors' contributions
CJ and FL designed the experiments, MY, JD and SF collected data. JL and SS analyzed the data and wrote the manuscript. FL and CJ confirm the authenticity of all the raw data. All authors reviewed and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by the ethics committee of Qingdao No. 6 People's Hospital [Approval no. (2018) 26] and written informed consent was obtained from all patients.
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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