- Open Access
Inactivation of ZSCAN18 by promoter hypermethylation drives the proliferation via attenuating TP53INP2-mediated autophagy in gastric cancer cells
Clinical Epigenetics volume 15, Article number: 10 (2023)
Zinc finger and scan domain containing 18 (ZSCAN18) belongs to the zinc finger transcription factor superfamily, which consists of hundreds of members that play critical roles in all steps of tumorigenesis.
This study aims to investigate the roles of ZSCAN18 in gastric cancer (GC). The expression level in GC and the clinicopathologic features of ZSCAN18 were detected by immunohistochemistry staining. Methylation of ZSCAN18 promoter in GC tissues and cell lines was analyzed via MassARRAY; the same method was used to detect GC cell lines demethylated by 5-aza-2′-deoxycytidine treatment. The biological function of ZSCAN18 in GC cells was verified by in vitro and in vivo experiments. The downstream molecular mechanism of ZSCAN18 was explored using RNA next-generation sequencing, immunofluorescence and chromatin immunoprecipitation.
Our work revealed ZSCAN18 expression was markedly reduced in GC tissues compared with adjacent normal tissues as a result of hypermethylation in GC. Likewise, ZSCAN18 expression was significantly reduced in a panel of GC cell lines as a result of the densely methylated ZSCAN18 promoter. Functionally, ZSCAN18 overexpression inhibited the biological progression of GC cells, which was characterized by weaken proliferation, enhanced autophagy and suppressed tumor growth. ZSCAN18 acted as a transcription factor and played an important role in binding to the promoter of tumor protein 53-induced nuclear protein 2 (TP53INP2), and we also confirmed the anti-tumor effect of TP53INP2 in GC. Furthermore, the knockdown of TP53INP2 alleviated the inhibiting effects of ZSCAN18 in GC cells by in vitro and in vivo experiments.
Collectively, this study unveiled that ZSCAN18 played an anticancer role in GC by promoting autophagy and transcriptional regulation of TP53INP2 and provided a promising target for the diagnosis and treatment of GC.
Gastric cancer (GC), as a complex heterogeneous disease, is the fifth most common cancer and the third most common cause of cancer deaths globally [1,2,3]. Although diagnostic and therapeutic strategies for advanced GC have improved significantly in recent years, the treatment remains unsatisfactory, and the prognosis remains poor. Therefore, the molecular mechanisms of GC pathogenesis should be elucidated to explore potential therapeutic targets for clinical use.
Zinc finger (ZNF) transcription factors (TF) represent the largest TF superfamily, and its members play critical roles in all aspects of cellular processes. Zinc finger and scan domain containing 18 (ZSCAN18) is a ZSCAN TF (a subfamily of ZNF TFs). ZSCAN18 is also known as ZNF447 and is located in chromosome 19q13.43. Recently, hypermethylation in the promoter of ZSCAN18 has been identified in various types of cancers, such as esophageal cancer , renal cell carcinoma , cholangiocarcinoma [6, 7], colorectal cancer [8, 9], GC [9,10,11], hepatocellular carcinoma , and pancreatic cancer [9,10,11]. Low protein expression of ZSCAN18 is reported in these malignancies, especially in gastrointestinal cancers. These findings strongly suggest that ZSCAN18 exerts anti-tumor effects. However, the mechanisms and functions of hypermethylated ZSCAN18 in GC remain poorly understood.
In this study, we analyzed the epigenetic regulation and functions of ZSCAN18 and revealed that promoter hypermethylation contributed to low ZSCAN18 expression in GC. We showed that ZSCAN18 hypermethylation in GC was correlated with prognostic outcomes. We also confirmed that ZSCAN18 high expression inhibited the proliferation of GC cells, both in vitro and in vivo. Our further investigation revealed that ZSCAN18 could bind to tumor protein 53-induced nuclear protein 2 (TP53INP2) promoter and promote autophagy, which might be related to the inhibitory effect of ZSCAN18 on cell proliferation. Most importantly, the knockdown of TP53INP2 alleviated the inhibiting effects of ZSCAN18 overexpression in GC cells. These results indicated that ZSCAN18 induced autophagy and suppressed GC proliferation through transcriptional regulation of TP53INP2. Moreover, ZSCAN18 expression may be involved in GC with a potential therapeutic target value.
Materials and methods
The mRNA expression data and methylation data were obtained from the Gene Expression Omnibus (GEO) database with the login numbers GSE33335 and GSE30601.
Tissue sample collection and follow-up
The tissues used for immunohistochemistry (IHC) were composed of 83 pairs of tumor and adjacent non-tumor tissues that were collected from patients with GC who underwent curative gastrectomy at Tianjin Medical University Cancer Hospital (Tianjin, China) between January 2004 and August 2007. All patients underwent standard follow-up after curative surgery. The median follow-up time was 22 months (range 3–70 months). The tissue used for the MassARRAY methylation test consisted of 97 cancerous tissues and 6 paracancer tissues from patients undergoing radical gastrectomy between January 2003 and July 2007 at Tianjin Medical University Cancer Hospital (Tianjin, China), of which 97 cancerous tissues were closely observed. The median follow-up time was 17 months (range 2–85 months). The clinical data included the patient’s age, sex, endoscopy result, chest X-ray, B-mode ultrasound and surgical methods. Between August and November 2019, we collected 30 pairs of GC and adjacent non-tumor tissues for RNA extraction. The study was conducted with patient consent. The experimental study protocol and the use of clinical data were approved by the Ethics Committee of the Cancer Institute of Tianjin Medical University and the Cancer Hospital of Tianjin Medical University (Tianjin).
Cell culture and transfection
The cell lines of MKN45, NCI-N87, BGC-823, MGC-803, SGC-7901, SNU-1, KATO-III and GES-1 were cultured in RPMI 1640 medium (Gibco, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS, HyClone) and 1% antibiotics (penicillin/streptomycin) (Gibco). AGS cells were cultured in F12k (Gibco) with 10% FBS and 1% antibiotics. The HEK293T cell line was cultured in Dulbecco’s modified Eagle medium (DMEM) (Gibco) with 10% FBS and 1% antibiotics. Cells were maintained at 37 °C with a 5% CO2 atmosphere. The expression levels of ZSCAN18 and TP53INP2 were enhanced by plasmids (plVX-IRES-Puro-ZSCAN18) and (plVX-IRES-Puro-TP53INP2), respectively, and an empty vector was transfected into the cells (pLVX-IRES-Puro-vector) as control. The shRNA against TP53INP2 interference sequence was synthesized (shTP53INP2, 5′-TGGACGGCTGGCTCATC-3). Western blot and quantitative real-time polymerase chain reaction (qRT-PCR) were used to verify the transfection efficiency.
Further 83 paired GC and matched adjacent non-tumor tissues were retrieved from Tianjin Medical University Cancer Hospital (Tianjin, China), Xijing Hospital of Air Force Medical University (Xi’an, China) and Renji Hospital of Shanghai Jiao Tong University School of Medicine (Shanghai, China) between August 2004 and December 2007, and sent to Shanghai Outdo Biotech Company (Shanghai, China) for tissue microarray analysis to evaluate the expression of ZSCAN18. The antibody concentrations of ZSCAN18 and TP53INP2 were 1:150 and 1:300, respectively. The staining intensity of ZSCAN18 and TP53INP2 was estimated by three independent pathologists without knowledge of the clinical data. The staining intensity was divided into 0 (negative), 1 (weak), 2 (medium), and 3 (strong) ranks. Zero and 1 were considered negative; 2 and 3, positive.
The western blot experiment was conducted in accordance with standard procedures. The primary antibodies used for this research were as follows: anti-ZSCAN18 (TA505326, OriGene), anti-VINCULIN (ab219649, Abcam), anti-p62/SQSTM1 (#16177S, CST), anti-LC3A/B (#12741S, CST) and anti-TP53INP2 (ab273012, Abcam).
Cell viability assay
Cell viability was detected using a Cell Counting Kit 8 (CCK-8) reagent. After the cell count, cells were placed in a 96-well culture plate; the AGS cell line had 1 × 103 cells per well, and the NCI-N87 cell line had 3 × 103 cells per well. Testing started 2 h after the addition of 10 µl of the CCK-8 reagent. AGS was tested once a day, and NCI-N87 was tested once every other day. Another way to assess cell viability was to measure adenosine triphosphate (ATP) levels using the Cell Titer-Glo assay (Promega, Cat#G7570). Chloroquine (CQ; HY-17589A) and rapamycin (RAP; HY-10219) were purchased from MedChemExpress (MCE, USA) and were treated at a concentration of 10 μM (CQ) and 100 nM (RAP) for 24 h, respectively. The ZSCAN18-overexpressed AGS, ZSCAN18-overexpressed NCI-N87 and control cells were cultured in 96-well plates with or without CQ/RAP.
Colony formation assay
The colony-forming method was used to detect the proliferation of GC cells. We conducted experiments on AGS and NCI-N87 cell lines using 1000 AGS cells per well and 8000 NCI-N87 cells per well. After the cell count, the cells were inoculated into 6-well plates and incubated at 37 °C for 12 to 14 days. Cell fluid was changed periodically until a visible clone formed.
Ten 4-week-old female BALB/C nude mice (Vital River) were purchased to construct a subcutaneous tumor xenograft. A total of 3 × 106 cells were injected into the lateral dorsal subcutaneous flank of nude mice. Xenograft tumor formation was measured every 4 days. Three weeks after injection, the nude mice were euthanized by cervical dislocation killing after intraperitoneal injection of 2% pentobarbital sodium (0.5 mL), and the tumor volume (V) was measured by the formula: V = 1/2 × length × (width)2. Tumor tissues were excised for immunohistochemistry.
AGS and NCI-N87 cells were laid 12 h in advance, and the cell density was approximately 30% on the next day. Cells were incubated with a concentration of 2 μM of 5-aza-2′-deoxycytidine (DAC, Sigma, St. Louis, MO). The liquid was changed every 24 h. The treatment lasted 96 h.
RNA sequencing and analysis
NCI-N87 cells were stably transfected with PLVX-IRES-Puro-ZSCAN18 or empty vector (PLVX-IRES-Puro). RNA from total samples was isolated and purified using TRIzol (Invitrogen, CA, USA). Then, NanoDrop ND-1000 (NanoDrop, Wilmington, DE, USA) was used to control the quantity and purity of total RNA. The captured mRNA was fragmented at 94 °C for 5 to 7 min using a magnesium ion fragmentation kit (NEBNext® RNA Fragmentation Module, article no. E6150S, USA). cDNA was synthesized from the segmented RNA using Invitrogen SuperScript™ II Reverse Transcriptase (article no. 1896649, CA, USA). Illumina NovaSeq™ 6000 (LC Bio Technology Co., Ltd., Hangzhou, China) was used for double-terminal sequencing according to the standard operation, and the sequencing mode was PE150. Cutadapt (https://cutadapt.readthedocs.io/en/stable, version for Cutadapt 1.9) was used to remove the joint plane raw data processing software. A significant difference was analyzed between samples, and the multiple of the difference (fold change [FC] > 2 or [FC] < 0.5 with a p value < 0.05) defined differentially expressed genes (DEGs), which were analyzed for Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment using R packs.
MassARRAY analysis of the methylation level of ZSCAN18
Instructions to extract cells or tissues using the DNA extraction kit (BioTeKe Corporation) were observed. The DNA samples to be tested were processed using a commercial NaHSO3 kit (ZYMO). The gene fragments to be detected were enriched and amplified by PCR reaction, and the product length was 200 to 700 bp. The PCR product was treated with shrimp alkaline phosphatase to remove free deoxyribonucleoside-5′-triphosphates (dNTPs) in the system. A transcriptase digestion reaction was followed by resin purification. The purified products of the resin were transported to a 384-well SpectroCHIP® bioarray (Agena, Inc.) using an Agena NanodispenserRS1000 dot sampling instrument (Agena, Inc.). EpiTYPER™ software provided advanced and convenient quantitative analysis of DNA methylation.
Binding motif prediction
The chromatin immunoprecipitation next-generation sequencing (ChIP-seq) information of ZSCAN18 was acquired from the Cistrome Data Browser database (http://cistrome.org/db/#) and then visualized using the UCSC browser. The predicted binding sequences at −100 bp to +2000 bp from the reference sequence (RefSeq) transcription start site were extracted from the U.S. National Library of Medicine (https://www.ncbi.nlm.nih.gov) and were then inputted into the ChIP-seq database of ZSCAN18. The DNA sequences were extracted from an obviously higher peak, and primers were designed in sections for the chromatin immunoprecipitation (ChIP) experiment.
ChIP experiments followed previous described protocol
The ChIP assay was performed using the ChIP-IT® Express Enzymatic Magnetic Chromatin Immunoprecipitation Kit & Enzymatic Shearing Kit (Cat No. 53009 & 53035, Active Motif, USA) according to the manufacturer's instructions. Briefly, stable ZSCAN18-expressing AGS or NCI-N87 cells and vector-expressing cells were cross-linked with formaldehyde, which were collected in centrifuge tubes for protein extraction. The chromatin was sheared to 200–1000 bp by enzymatic shearing from extracted cross-linked nuclei. The sheared chromatin was incubated with an antibody of ZSCAN18 (UM500081, OriGene); the antibody-bound DNA complexes were precipitated through the use of magnetic Protein G-coupled beads. The same amount of non-specific immunoglobulin G (IgG) is used as control. The captured chromatin was then eluted, the cross-links were reversed, and the recovered DNA was analyzed by qRT-PCR using the primer of TP53INP2 (5′-GGTGGGAAAGCAGAGTGTGT-3).
The GC cells were transfected with recombinant mRFP‐GFP‐LC3 adenovirus. In green- and red‐merged pictures, autophagosomes were shown as yellow puncta, while autolysosomes were shown as red puncta. Otherwise, autophagic flux was detected using fluorescence microscope (Zeiss).
IBM SPSS Statistics (version 24.0; Armonk, NY, USA) and GraphPad Prism 8 software (GraphPad Software Inc., La Jolla, CA, USA) were used to analyze the data for this study. The t test was used to compare statistical differences between the two groups. The chi-squared test and Fisher’s exact test were used to analyze the relationship between methylation and various clinicopathological parameters. Overall survival was determined by log-rank test and the Kaplan–Meier method. The Spearman correlation test was used to analyze the correlation between gene expression and the methylation level. A receiver operating characteristic (ROC) curve was used to evaluate the diagnostic value of methylation sites in cancerous and adjacent tissues. In univariate analysis, survival differences were estimated using the Kaplan–Meier method (log-rank test), and independent prognostic factors were subsequently identified in Cox proportional risk regression models for multivariate analysis. p < 0.05 was considered statistically significant.
Downregulation of ZSCAN18 in primary GC is associated with poor survival
Initially, bioinformatics analysis of the data from The Cancer Genome Atlas (TCGA) datasets showed that expression of ZSCAN18 was depressed in a variety of cancers (Fig. 1A), and analysis from the public datasets (GSE33335) showed that ZSCAN18 is downregulated in GC samples (Fig. 1B). Subsequently, we compared the mRNA expression of ZSCAN18 in 30 GC tissue samples and matched adjacent non-tumor tissue samples by qRT-PCR. Accordingly, ZSCAN18 was downregulated significantly in the primary tumor compared to that in the adjacent non-tumor tissues (Fig. 1C). Next, using IHC analysis, we semi-quantified ZSCAN18 protein levels of 83 fresh gastric adenocarcinoma tissues and matched adjacent non-tumor tissues. IHC demonstrated that ZSCAN18 was positively stained in the nuclei of gastric mucosal cells and that its protein levels were considerably lower in GC tissues than in matched adjacent non-tumor tissues (Fig. 1D). Kaplan–Meier analysis showed that the overall survival of patients with negative expressions of ZSCAN18 was significantly shorter than the survival of patients with positive expressions (Fig. 1E). Tumor size, depth of tumor invasion (pT3–4 vs pT1-2), lymph node metastasis (positive vs negative) and low expression of ZSCAN18 predicted an increased risk of cancer-related death in univariate analysis (Table 1). Multivariate analysis revealed that depth of tumor invasion (pT3–4 vs pT1-2), lymph node metastasis (positive vs negative) and expression of ZSCAN18 were independent prognostic factors (Fig. 1F). These results demonstrate that ZSCAN18 is downregulated in primary GC and is associated with poor survival.
ZSCAN18 is frequently hypermethylated in primary GC and is associated with poor survival
To explore the regulation mechanism of ZSCAN18 in GC, we focused on epigenetic alterations, especially DNA promoter methylation. Bioinformatics analysis of the data from the public dataset (GSE30601) confirmed a high methylation level of ZSCAN18 in GC (Fig. 1G). The MassARRAY analysis spanned the promoter region from − 209 to 280, including 50 CpG islands (of which 41 were detectable), and was used to evaluate the methylation level. The level of ZSCAN18 methylation was investigated in 97 primary GC tissues and 6 adjacent non-tumor tissues by MassARRAY analysis, which identified significantly higher methylation of ZSCAN18 in GC (Fig. 1H). Aberrant ZSCAN18 promoter hypermethylation in various CpG islands (CpG11.19.39, CpG23.37.44, CpG26.27 and CpG45.46) was detected more often in GC tissues than in adjacent non-tumor tissues (Fig. 1I). As shown in the Kaplan–Meier survival curves, patients with GC and high ZSCAN18 methylation had significantly shorter survival times compared with those with GC who had low ZSCAN18 methylation (Fig. 1J). Tumor size, depth of tumor invasion (pT3–4 vs pT1-2), lymph node metastasis (positive vs negative) and hypermethylation in CpG45.46 predicted an increased risk of cancer-related death in univariate analysis (Table 2). Additional multivariate analysis showed that ZSCAN18 promoter hypermethylation in CpG45.46, depth of tumor invasion (pT3–4 vs pT1-2) and lymph node metastasis (positive vs negative) were independent prognostic factors (Fig. 1K). Collectively, these results reveal that ZSCAN18 is frequently hypermethylated in primary GC and that hypermethylation contributes to poor survival in patients with GC; also, the methylation level of CpG45.46 may be an important marker of prognosis.
The silencing of ZSCAN18 mediated by promoter hypermethylation in GC cells
We examined the mRNA expression of ZSCAN18 in 8 GC cell lines by qRT-PCR. Reduced expression of ZSCAN18 was found in 8 GC cell lines compared with the human gastric epithelial cell line (GES-1) (Fig. 2A). We next explored the role of promoter methylation in the regulation of ZSCAN18 by MassARRAY analysis. Consistent with the reverse tendency of ZSCAN18 expression, hypermethylation was detected in these GC cell lines (Fig. 2B). A significant negative correlation was observed between mRNA expression and the methylation level of ZSCAN18 in the cell lines we detected (AGS, MGC-803, MKN45, SNU-1, BGC-823, NCI-N87, KATO-III and SGC-7901) (Fig. 2C). To confirm whether promoter methylation mediated ZSCAN18 silencing, two methylated cell lines (AGS and NCI-N87) that showed silencing of ZSCAN18 were treated with the DNA methyltransferase inhibitor DAC, and the mRNA expression of ZSCAN18 was restored in both lines (Fig. 2D). The change in the ZSCAN18 methylation level was synchronously validated by MassARRAY analysis in AGS cells (Fig. 2E). Furthermore, the decreased methylation level of ZSCAN18 was confirmed in a variety of CpG islands (Fig. 2F). These results indicate that promoter hypermethylation is associated with the transcriptional silence of ZSCAN18 in GC cells; moreover, additional demethylation restores the expression of ZSCAN18.
Rescue of ZSCAN18 expression inhibits the proliferation of GC cells via triggering autophagy
To elucidate the functional significance of ZSCAN18 in GC, we first upregulated ZSCAN18 in AGS and NCI-N87 cells, and overexpression of ZSCAN18 was identified by qRT-PCR and western blot (Fig. 3A). The CCK-8 assay showed that ZSCAN18 overexpression could inhibit the proliferation of both AGS and NCI-N87 cells (Fig. 3B). This inhibitory effect on cell growth was also confirmed with a colony formation assay in both AGS and NCI-N87 cells (Fig. 3C). Subsequently, NCI-N87 cell lines transfected with ZSCAN18 overexpression or empty vector control cells were used to establish xenograft tumors in mice to examine whether ZSCAN18 could suppress the growth of GC cells in vivo. The tumor volumes were 52.67 ± 13.58 mm3 in xenografted mice with ZSCAN18-overexpressed NCI-N87 cells and 167.7 ± 10.89 mm3 in xenografted mice with empty vector control NCI-N87 cells (Fig. 3D). The tumor growth was significantly lower in ZSCAN18-transfected nude mice than in the vector control mice, suggesting that ZSCAN18 does function as a tumor suppressor in GC. To gain insights into the molecular mechanisms underlying the tumor inhibition of ZSCAN18, we analyzed the downstream signaling pathways modulated by ZSCAN18 through RNA next-generation sequencing (RNA-seq) in ZSCAN18-overexpressed and control NCI-N87 cells. These DEGs were classified into different KEGG enrichment pathways, including the autophagy pathway, which was well established as playing an important role in carcinogenesis (Fig. 3E). To investigate the role of ZSCAN18 in the promotion of GC cells autophagy, autophagy‐related protein expression was assayed via western blotting. We observed increased LC3-II/LC3-I expression and decreased p62/SQSTM1 expression in AGS and NCI-N87 cells transfected with the ZSCAN18 overexpressing plasmid compared with the empty vector (Fig. 3F). In addition, we detected autophagic vesicles via fluorescence microscope. The number of yellow puncta increased significantly in the ZSCAN18 overexpression group, which confirmed the increase in the number of autophagosomes (Fig. 3G). To further illuminate the role of ZSCAN18-induced autophagy on cell proliferation, ZSCAN18-overexpressed AGS and ZSCAN18-overexpressed NCI-N87 cells were pretreated with CQ and RAP, respectively. We observed increased LC3-II/LC3-I expression and decreased p62/SQSTM1 expression in ZSCAN18-overexpressed AGS and ZSCAN18-overexpressed NCI-N87 cells pretreated with RAP compared with the empty vector and reversed results in p62/SQSTM1 expression by the addition of CQ (Fig. 3H). When co-incubated with CQ, the cell viability was significantly enhanced in ZSCAN18-overexpressed AGS and ZSCAN18-overexpressed NCI-N87 cells (Fig. 3I). Conversely, the cell viability was significantly inhibited in ZSCAN18-overexpressed AGS and ZSCAN18-overexpressed NCI-N87 cells when co-incubated with RAP (Fig. 3I). Above all, these findings demonstrated that the proliferation was inhibited, while the autophagy was enhanced in ZSCAN18 overexpression AGS and NCI-N87 cells indicating a modulation effect between ZSCAN18-induced autophagy and cell proliferation.
TP53INP2 is transcriptionally regulated by ZSCAN18 in GC cell lines
As IHC results showed, ZSCAN18 localized mainly to the nucleus; thus, it is reasonable to speculate that ZSCAN18 might be implicated in the regulation of gene expression. We found that the expressions of 510 genes (DEGs) were significantly changed (FC > 2, p < 0.05) in NCI-N87 cells; among them, 289 genes were upregulated, whereas 221 were downregulated. Among these DEGs, TP53INP2 had attracted our attention because it is related to autophagy  (Fig. 4A). ZSCAN18 was positively correlated with TP53INP2 expression in GC tissues, according to bioinformatics analysis (Fig. 4B). The expression levels of TP53INP2 in AGS and NCI-N87 cells after ZSCAN18 overexpression were detected by qRT-PCR and western blot (Fig. 4C). ChIP-seq analysis according to bioinformatics analysis showed that ZSCAN18 enrichment was found in the promoter region of TP53INP2 (Fig. 4D). ChIP assay further confirmed that ZSCAN18 overexpression could bind more to the TP53INP2 promoter region than the empty vector (Fig. 4E). Taken together, these data suggest that TP53INP2 was transcriptional regulated by ZSCAN18.
TP53INP2 attenuated the GC cell proliferation through inducing autophagy
In most of the carcinomas, including GC, the expression of TP53INP2 was lower than in adjacent tissues, as bioinformatics analysis of the TCGA public datasets indicated (Fig. 5A, B) (http://ualcan.path.uab.edu). We examined the expression level of TP53INP2 in primary GC samples by IHC staining, which showed that the signal expression intensity of TP53INP2 in GC tissues was significantly lower than that in adjacent normal gastric tissues (Fig. 5C). To explore the biological functions of TP53INP2, TP53INP2 was overexpressed by transfection with TP53INP2 overexpression plasmid (Fig. 5D). Overexpression of TP53INP2 resulted in significantly inhibited cell growth (Fig. 5E) as well as reduced colony formation (Fig. 5F). TP53INP2 could induce autophagy by downregulating p62/SQSTM1, upregulating LC3‐II/LC3-I (Fig. 5G) and reducing the number of autophagosomes (Fig. 5H). These data indicate that TP53INP2 suppresses GC via inhibiting cell proliferation and inducing autophagy.
ZSCAN18-induced suppression of GC cell proliferation is mediated by TP53INP2
Functional recovery experiments were performed to determine whether ZSCAN18 and TP53INP2 had a synergistic effect in GC. Three groups of cells were established in AGS and NCI-N87 cells: ZSCAN18 overexpression and TP53INP2 knockdown (ZSCAN18 + shTP53INP2), ZSCAN18 overexpression and empty vector (ZSCAN18 + shVector), empty vector and empty vector (Vector + shVector). Compared with the group of ZSCAN18 + shVector, the malignant progression of AGS and NCI-N87 cells in ZSCAN18 + shTP53INP2 group was significantly enhanced, which was characterized by promoted proliferation in vitro and in vivo (Fig. 6A–C), and impeded autophagy (Fig. 6D, E). In brief, the loss-/gain-of-function assays demonstrated that the knockdown of TP53INP2 could alleviate the inhibiting effects of ZSCAN18 overexpression in AGS and NCI-N87 cells.
In this study, we provide substantial evidence of a suppressive effect of ZSCAN18 on GC. We found that ZSCAN18 is widely downregulated in GC tissues and in most GC cell lines, suggesting a suppressive effect on carcinogenesis. As confirmed by demethylation treatment and MassARRAY analyses, these decreased expressions are mostly attributed to ZSCAN18 promoter hypermethylation in various CpG islands. However, ZSCAN18 hypermethylation was not detected in normal gastric mucosal tissues or GES-1 cells, suggesting that the hypermethylation of the ZSCAN18 promoter appears to follow a chronological sequence during carcinogenesis and is involved in the early stage of the multistep process of GC [9, 13, 14]. This study revealed that promoter hypermethylation is a unique mechanism of ZSCAN18 inactivation in GC. In addition, we confirmed for the first time, to our knowledge, that downregulation of ZSCAN18 with hypermethylation in CpG44.45 is associated with poor survival in primary GC; this finding suggests that ZSCAN18 may serve as a biomarker of poor prognosis [15,16,17]. Furthermore, the restorability of CpG44.45 after treatment with DAC (also known as decitabine, a chemotherapy agent) indicates that ZSCAN18 may be a potential target for an anti-tumor drug.
Given that ZSCAN18 reduction leads to poor survival, it is reasonable to postulate that ZSCAN18 could affect the progression and development of GC. Furthermore, the tumor-suppressive function of ZSCAN18 in GC was investigated both in vitro and in vivo. First, gain-of-function experiments using ZSCAN18 were performed in AGS and NCI-N87 cells, and the effect of ZSCAN18 on the proliferation of these cells was examined using CCK-8 and colony formation assays. The results showed that ZSCAN18 overexpression inhibited GC cell proliferation. In addition, decreased tumor growth resulting from ZSCAN18 overexpression was observed in nude mice and supports the inhibitory role of ZSCAN18 in GC. Taken together, these results confirm the crucial role of ZSCAN18 as a functional anti-tumor gene through suppression of cell proliferation in GC.
To extend our investigation of molecular mechanisms, we analyzed downstream signaling pathways regulated by ZSCAN18 through RNA-seq due to its role as a transcription factor. We elucidated the molecular mechanism of the tumor-suppressive function of ZSCAN18: regulation of the autophagy signaling pathway. In solid tumors, although autophagy has emerged as an attractive therapeutic target, the role of autophagy in tumor cells is complex and depends on tumor type and stage [18,19,20,21]. In this study, when ZSCAN18 is overexpressed, we find that autophagy is constitutively activated in AGS and NCI-N87 cells through observation on the elevated conversion of LC3-I to II, decreased expression of p62/SQSTM1, and increased autophagosomes. The proliferation modulated by ZSCAN18 in AGS and NCI-N87 cells is further confirmed by co-incubated with CQ (known as an autophagy inhibitor) and RAP (known as an autophagy activator), respectively.
Our experiment confirmed that abnormal overexpression of TP53INP2 caused by the ZSCAN18 upregulation plays an extremely important role in the suppression of GC. Moreover, TP53INP2 is a key positive regulator of autophagy and may act as a novel autophagic adaptor through the recruitment of ubiquitinated substrates to autophagosomes for degradation [22,23,24,25]. In our study, we confirmed that overexpression of TP53INP2 can enhance autophagy in GC cells.
Based on our data, we speculate that there may be a link between ZSCAN18 and TP53INP2. As a transcription factor, ZSCAN18 may transcriptively regulate TP53INP2 and bind to the promoter region of TP53INP2 to accelerate transcription and increased its protein expression. In addition, ChIP assay further confirmed that overexpression of ZSCAN18 could bind to the TP53INP2 promoter region and showed an interaction between ZSCAN18 and TP53INP2. We further confirmed the biological effects of ZSCAN18 regulation on TP53INP2 by in vitro and in vivo loss-/gain-of-function assays. Together, these data demonstrate that ZSCAN18 inhibits the malignant behavior of GC cells by binding to the TP53INP2 promoter.
Overall, the low expression of ZSCAN18 in GC tissues and cells is correlated with hypermethylation in the promoter region, which has clinical value in predicting the prognosis of GC. ZSCAN18 inhibits malignant behavior in GC by binding to the TP53INP2 promoter region and promoting autophagy, which may contribute to the development of a promising target for carcinoma diagnosis and treatment.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.
Zinc finger and scan domain containing 18
Tumor protein 53-induced nuclear protein 2
Gene Expression Omnibus
Fetal bovine serum
Dulbecco’s modified Eagle medium
Quantitative real-time polymerase chain reaction
Cell Counting Kit 8
Differentially expressed genes
Kyoto Encyclopedia of Genes and Genomes
Chromatin immunoprecipitation next-generation sequencing
Receiver operating characteristic
The Cancer Genome Atlas
Human gastric epithelial cell line
RNA next-generation sequencing
Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2021. CA Cancer J Clin. 2021;71(1):7–33.
Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209–49.
Smyth EC, Nilsson M, Grabsch HI, van Grieken NC, Lordick F. Gastric cancer. Lancet. 2020;396(10251):635–48.
Oka D, Yamashita S, Tomioka T, Nakanishi Y, Kato H, Kaminishi M, et al. The presence of aberrant DNA methylation in noncancerous esophageal mucosae in association with smoking history: a target for risk diagnosis and prevention of esophageal cancers. Cancer. 2009;115(15):3412–26.
Morris MR, Ricketts CJ, Gentle D, McRonald F, Carli N, Khalili H, et al. Genome-wide methylation analysis identifies epigenetically inactivated candidate tumour suppressor genes in renal cell carcinoma. Oncogene. 2011;30(12):1390–401.
Andresen K, Boberg KM, Vedeld HM, Honne H, Hektoen M, Wadsworth CA, et al. Novel target genes and a valid biomarker panel identified for cholangiocarcinoma. Epigenetics. 2012;7(11):1249–57.
Andresen K, Boberg KM, Vedeld HM, Honne H, Jebsen P, Hektoen M, et al. Four DNA methylation biomarkers in biliary brush samples accurately identify the presence of cholangiocarcinoma. Hepatology. 2015;61(5):1651–9.
Mitchell SM, Ross JP, Drew HR, Ho T, Brown GS, Saunders NF, et al. A panel of genes methylated with high frequency in colorectal cancer. BMC Cancer. 2014;14:54.
Vedeld HM, Andresen K, Eilertsen IA, Nesbakken A, Seruca R, Gladhaug IP, et al. The novel colorectal cancer biomarkers CDO1, ZSCAN18 and ZNF331 are frequently methylated across gastrointestinal cancers. Int J Cancer. 2015;136(4):844–53.
Jiang H, Gu J, Du J, Qi X, Qian C, Fei B. A 21-gene support vector machine classifier and a 10-gene risk score system constructed for patients with gastric cancer. Mol Med Rep. 2020;21(1):347–59.
Yu CB, Zhu LY, Wang YG, Li F, Zhang XY, Dai WJ. Systemic transcriptome analysis of hepatocellular carcinoma. Tumour Biol. 2016;37(10):13323–31.
You Z, Xu Y, Wan W, Zhou L, Li J, Zhou T, et al. TP53INP2 contributes to autophagosome formation by promoting LC3-ATG7 interaction. Autophagy. 2019;15(8):1309–21.
Leung WK, Yu J, Ng EK, To KF, Ma PK, Lee TL, et al. Concurrent hypermethylation of multiple tumor-related genes in gastric carcinoma and adjacent normal tissues. Cancer. 2001;91(12):2294–301.
Qu Y, Dang S, Hou P. Gene methylation in gastric cancer. Clin Chim Acta. 2013;424:53–65.
Tahara T, Arisawa T. DNA methylation as a molecular biomarker in gastric cancer. Epigenomics. 2015;7(3):475–86.
Matsuoka T, Yashiro M. Biomarkers of gastric cancer: current topics and future perspective. World J Gastroenterol. 2018;24(26):2818–32.
Abbas M, Faggian A, Sintali DN, Khan GJ, Naeem S, Shi M, et al. Current and future biomarkers in gastric cancer. Biomed Pharmacother. 2018;103:1688–700.
Ivan D, Terje J, Vladimir K. Selective autophagy in cancer development and therapy. Cancer Res. 2010;70(9):3431–4.
Gozuacik D, Kimchi A. Autophagy as a cell death and tumor suppressor mechanism. Oncogene. 2004;23(16):2891–906.
Shintani T, Klionsky DJ. Autophagy in health and disease: a double-edged sword. Science. 2004;306(5698):990–5.
Kondo Y, Kanzawa T, Sawaya R, Kondo S. The role of autophagy in cancer development and response to therapy. Nat Rev Cancer. 2005;5(9):726–34.
Zhang W, Li P, Wang S, Cheng G, Wang L, Mi X, et al. TP53INP2 promotes bovine adipocytes differentiation through autophagy activation. Animals (Basel). 2019;9(12):1060.
Xu Y, Wan W. TP53INP2 mediates autophagic degradation of ubiquitinated proteins through its ubiquitin-interacting motif. FEBS Lett. 2019;593(15):1974–82.
Xu Y, Wan W. The bifunctional role of TP53INP2 in transcription and autophagy. Autophagy. 2020;16(7):1341–3.
Ivanova S, Polajnar M, Narbona-Perez AJ, Hernandez-Alvarez MI, Frager P, Slobodnyuk K, et al. Regulation of death receptor signaling by the autophagy protein TP53INP2. EMBO J. 2019;38(10): e99300.
This work was jointly funded by the Distinguished Professor of Tianjin (JTZB  No. 120), Tianjin Key Medical Discipline (Specialty) Construction Project (TJYXZDXK-009A) and the National Key R&D Program of China (Grant No. 2016YFC1303200).
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This research was approved by the Ethics Committee of Tianjin Medical University Cancer Hospital, and oral and written informed consents were obtained from all patients before enrolling in the research program. The in vivo assay using nude mice was approved by the Institutional Animal Care and Use Committee of Tianjin Medical University Cancer Hospital.
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Li, B., Ren, B., Ma, G. et al. Inactivation of ZSCAN18 by promoter hypermethylation drives the proliferation via attenuating TP53INP2-mediated autophagy in gastric cancer cells. Clin Epigenet 15, 10 (2023). https://doi.org/10.1186/s13148-023-01425-9
- Gastric cancer