tRNA-Derived Fragment tRF-Glu-TTC-027 Regulates the Progression of Gastric Carcinoma via MAPK Signaling Pathway

Transfer RNA-derived RNA fragments (tRFs) belong to non-coding RNAs (ncRNAs) discovered in most carcinomas. Although some articles have demonstrated the characteristics of tRFs in gastric carcinoma (GC), the underlying mechanisms still need to be elucidated. Meanwhile, it was reported that the MAPK pathway was momentous in GC progression. Thus we focused on investigating whether tRF-Glu-TTC-027 could act as a key role in the progression of GC with the regulation of the MAPK pathway. We collected the data of the tRNA-derived fragments expression profile from six paired clinical GC tissues and corresponding adjacent normal samples in this study. Then we screened tRF-Glu-TTC-027 for analysis by using RT-PCR. We transfected GC cell lines with tRF-Glu-TTC-027 mimics or mimics control. Then the proliferation, migration, and invasion assays were performed to assess the influence of tRF-Glu-TTC-027 on GC cell lines. Fluorescence in situ hybridization assay was conducted to confirm the cell distribution of tRF-Glu-TTC-027. We confirmed the mechanism that tRF-Glu-TTC-027 influenced the MAPK signaling pathway and observed a strong downregulation of tRF-Glu-TTC-027 in clinical GC samples. Overexpression of tRF-Glu-TTC-027 suppressed the malignant activities of GC in vitro and in vivo. MAPK signaling pathway was confirmed to be a target pathway of tRF-Glu-TTC-027 in GC by western blot. This is the first study to show that tRF-Glu-TTC-027 was a new tumor-suppressor and could be a potential object for molecular targeted therapy in GC.


INTRODUCTION
According to the report issued by the National Cancer Registry in 2015, the statistical results of the disease show that the number of cases of gastric cancer (GC) in China is about 679,100, second only to lung cancer (733,300) and higher than esophageal cancer (477,900) and liver cancer (466,100). The total number of deaths due to gastric cancer is approximately 498,000 which is also second only to lung cancer, ranking second in tumor mortality. Despite the global downward trend of incidence and mortality of gastric cancer, the corresponding data is still at a relatively high level in China. Therefore, for a long time in the future, gastric cancer will still be one of the major public health issues in China (1,2).
tRNA-derived small RNAs (tsRNAs) can be classified into two kinds of ncRNAs, tRFs and tiRNAs. Transfer RNA-derived RNA fragments (tRFs) are derived from mature or precursor tRNAs and are composed of 14-30 nt in length approximately. tiRNAs, consist of 29-50 nt in length, are generated by spliced anticodon loop of tRNA (3). Fu et al. reported that the generation of tiRNAs has been discovered to occur through specific ribonucleases such as Angiogenin (4,5). Transfer RNA-derived RNA fragments (tRFs) and transfer RNA-derived stress-induced RNA (tiRNAs) belong to ncRNAs. These RNAs can be both produced under the circumstance of stress (6). It should be pointed out that tRFs and tiRNAs are reported to emerge from ribonucleolytic splicing of tRNAs by Dicer (7) and RNase Z (8). Meanwhile, tiRNAs can be classified into 5' tiRNAs and 3' tiRNAs. tRNA derivatives are found related to Argonaute proteins, and they could target mRNA 3'UTR to act as the RNA silencer (9,10). Some studies have revealed that tRNA derivatives could influence tumor proliferation, DNA damage repair, and the regulation of tumor-related signaling pathways via mRNA silencing (6,(11)(12)(13). Generally, it showed that tRFs and tiRNAs could act as novel potential biomarkers and cancer treatment targets.
Concerning this study, we screened out several differential expressed tRNA derivatives based on high-throughput sequencing. Through the exploration of the biological functions of GC cell lines and the verification of the expression level of gastric cancer tissues, we selected tRF-Glu-TTC-027 as the target of our further research. Little is known about the function of tRF-Glu-TTC-027 in gastric cancer as it is a brand new tRNA derivative. With the multi-dimensional bioinformatics analysis of the target genes of tRNA derivatives in the high-throughput sequencing files, we discovered a few signaling pathways responsible for the change of the biological characteristics, especially the MAPK signaling pathway. In our study, tRF-Glu-TTC-027 was downregulated in gastric cancer tissues, with an inverse correlation with tumor size and histology. Meanwhile, tRF-Glu-TTC-027 declined the progression of GC cells in vitro and suppressed tumor growth of gastric cancer in vivo. Our study concludes that tRF-Glu-TTC-027 plays an inhibitory role in gastric cancer.

Tissue Specimens
All the collected human gastric cancer tissues came from The Affiliated Cancer Hospital of Nanjing Medical University between 2016 and 2017, and the patients' informed consents were obtained. Our hospital's ethics committee evaluated and authorized this experiment prior to its implementation (NYDLS-2019-919). At the same time, we carefully read and abided by the Declaration of Helsinki. After the gastric cancer tissues were obtained, we strictly abided by the relevant tissue handling specifications and froze them in the refrigerator at -80°C.

tRFs&tiRNAs Expression Analysis
In our high-throughput sequencing files, the expression data of tRFs and tiRNAs were presented in counts and normalized to total aligned reads (CPM). The R package edgeR was utilized to screen the tRFs and tiRNAs. We used Fold Change (cutoff 1.5) and P-value (cutoff 0.05) for screening differentially expressed tRFs and tiRNAs. Principal Component Analysis (PCA), Correlation Analysis, Venn plots, Hierarchical clustering, Scatter plots, and Volcano plots were analyzed in R software or Perl environment. We utilized the GO and KEGG analysis on the potential targets of tRNA derivatives. Analysis of Biological Process (BP), Cellular Component (CC), and Molecular Function (MF) was presented with R software in GO analysis. P < 0.05 was considered significantly enriched in a certain process. Pathway clustering was conducted using KEGG analysis. We applied the enrichment score to indicate the significance of correlation. To elucidate the GC-related pathways more comprehensively, we acquired microarray profile GSE65801 in the GEO database and TCGA-STAD database. We then undertook the KEGG and GSEA analysis to further investigate the possible biological characteristics of GC.

Cell Culture and Transfection
We obtained the GC cell lines NCI-N87, HGC-27, BGC-823, SGC-7901, and GES-1 from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). GES-1 cell line was grown in 10% FBS DMEM medium. Medium for HGC-27, BGC-823, and SGC-7901 was RPMI 1640 with 10% FBS, for NCI-N87 was RPMI 1640 medium with 15% FBS. All media were purchased from ThermoFisher. We incubated the cell lines in a humidified incubator at 37°C with 5% CO2. The GC cells were seeded in a 6-well plate at a cell density of 20%-40%. 24 hours later, we used Lipofectamine 2000 (ThermoFisher, USA) to transfect tRF mimics or inhibitors (Ribobio, Guangzhou, China) (50 nM) into GC cells. We selected p38 MAPK pathway inhibitor (p38 MAPK-IN, MCE, USA) to act as the positive control of tRF-Glu-TTC-027. The detailed steps are available in our previous study (14). The sequences of the tRF mimic and corresponding control group were listed in Table 1. RNA Extraction, Reverse Transcription, and Quantitative Real-Time PCR Green Mix, 0.8 mL forward primer, and 0.8 mL reverse primer). PCR reaction conditions were 95°C for 30 sec, 40 cycles of 95°C for 5 sec and 60°C for 20 sec. U6 was used as an internal control. The detailed steps are available in our previous study (14). The primers used in qPCR were presented in Table 1. The relative expression was analyzed with the 2 -DDCt method.

Fluorescent In Situ Hybridization (FISH)
After the cells were treated with 4% paraformaldehyde, the cell membranes were permeabilized by Triton-100 (Beyotime, Shanghai, China) for 5 min at 4°C. Next, we added the hybridization solution mixed with Cy3-labelled tRF-Glu-TTC-027 to the permeabilized cells to locate the tRF-Glu-TTC-027 in GC cells. We stained the GC nuclei with DAPI and captured the pictures with a fluorescence microscope.

Cell Proliferation Assay and Colony Formation Assay
A certain number (2 x 10 3 ) of transfected GC cells were transferred to a 96-well plate, and then we added 10ul CCK8 solution (Dojindo, Japan) into each well to measure the OD value in 450 nm by the microplate reader after 2 hours of incubation at 0, 24, 48, 72 and 96 hours. We added 1,000 transfected cells into each well of the 6-well plate, and these GC cells were cultured for 10-14 days. Subsequently, we terminated the cultivation with 4% paraformaldehyde as soon as the macroscopic clones were observed. The 1% crystal violet was used to stain the clones and the numbers were counted using Image J software.

Edu Assay
Cell-Light EdU Apollo In Vitro Kit (Ribobio, Guangzhou, China) for EdU assay was utilized to compare the growth ability of the transfected GC cell. NCI-N87 and HGC-27 cell lines were transfected with tRF-Glu-TTC-027 mimics or mimics control, then 4 x 10 3 transfected cells were transferred into each well of the 96-well plate. We diluted the EdU solution with complete medium to prepare enough 50 mM EdU medium. And EdU medium was then added into each well to incubate the cells for two hours. After the fixation, permeabilization, and staining, we captured the images with a fluorescence microscope.

Migration and Invasion Assays
For wound healing assay, GC cells were seeded in a 6-well plate with 1.5×10 6 cells/well 24 hours before the experiment, and the tRF-Glu-TTC-027 mimics group and mimics control group were plated in three wells each. On the day of the experiment, we used a pipette tip to make a "+" mark in the 6-well plate and washed the exfoliated cells with PBS buffer. Then we took a picture and recorded the width of the scratch, and added 2 mL of complete medium to each well for culture. After 24h, we captured a picture and recorded the width of the scratch again. Percentage of gap closure = (0h scratch width -24h scratch width)/0h scratch width x 100%. For transwell migration and invasion assays, we took GC cells in the logarithmic growth phase to prepare the cell suspension with a cell density of 2 x 10 6 /mL using the serum-free medium. The upper layer of the transwell chamber with or without matrigel was then filled with 200 mL cell suspension, and the lower chamber was filled with 600 mL complete medium. After the incubation for 24 h in the incubator, we removed the liquid in the chamber's upper layer and carefully cleaned off the non-penetrated cells with a cotton swab. The polycarbonate membrane of the chamber was stained with hematoxylin, and we counted the number of penetrated cells under an optical microscope. Our previous research has described the specific steps in detail (14).

Cell Cycle Determination
NCI-N87 and HGC-27 cells were first harvested after 48 hours of transfection and the cell suspension was then centrifuged. Subsequently, we washed the cell pellet three times with icecold PBS and conducted the fixation with 70% ethanol. Afterward, we resuspended the cells in the PI-staining solution to perform the flow cytometry analysis.

Western Blot
The supernatant of the cell lysates was transferred to another clean centrifuge tube, and we used the BCA protein assay kit (ThermoFisher, USA) to detect the protein concentration. Then we performed gel electrophoresis (10% SDS-PAGE) and transferred the protein to a polyvinylidene fluoride membrane. The membrane was immersed in 5% skimmed milk for one hour and treated with the primary antibodies at 4°C with gentle tremors overnight. Next, the secondary antibody was added to block the membrane for two hours. We used the chemiluminescence method to develop and measure the gray band. Antibody dilutions and manufacturers are provided in Table 2.

Subcutaneous Xenograft Experiments
We obtained the five-week-old Balb/c female nude mice from the Shanghai Experimental Animal Center of the Chinese Academic of Sciences (Shanghai, China). The mice were randomly assigned to NS, tRF-Glu-TTC-027 NC, tRF-Glu-TTC-027 agomir groups (tRF-Glu-TTC-027 overexpression), and 1.2 x 10 6 treated NCI-N87 cells were then subcutaneously injected into their right flanks. tRF-Glu-TTC-027 NC and tRF-Glu-TTC-027 agomir were designed by Ribobio company (Ribobio, Guangzhou,  China). We measured the tumor sizes every three days. 40 days later, mice were sacrificed and the tumors were resected and sliced for IHC analysis and immunofluorescence assay. The tumor weight was measured and the volume was determined using the formula: 1/2 x (length x width 2 ).

Immunohistochemistry (IHC)
The paraffin-embedded tissue sections were deparaffinized and dehydrated. Then the sections were blocked with immunostaining blocking solution for 15 minutes at RT. Afterward, they were incubated in the Ki67 primary antibody ( Table 2) and secondary antibody for one hour, respectively. DAB substrate was used for staining. We counter-stained the cell nucleus with hematoxylin for two minutes and dehydrated the sections with ethanol. Images were captured by a microscope.

Immunofluorescence Staining
The tissue sections were infiltrated with PBS and rewarmed for 20 minutes. Then permeabilization was conducted using 0.5% Triton X-100 (prepared in PBS) at RT for 20 minutes. Next, we applied goat serum to block the tissue section for 30 minutes, and then the diluted primary antibody (Ki67) and fluorescent secondary antibody were used to incubate with each slide successively. Afterward, we immersed the slides with PBST and stained the specimens with DAPI. All the collected images were observed under a fluorescence microscope.

Statistical Analysis
We applied SPSS 19.0 (IBM, Chicago, USA) and GraphPad Prism 6 (San Diego, CA, USA) to deal with the data. Data were presented as mean ± SD. The Chi-square test or Fisher's exact test was applied to compare the composition ratio of two or more samples and analyze the correlation of two categorical variables. The Kaplan-Meier technique was used to evaluate the follow-up data, and the log-rank test was performed to assess the differences between groups. To compare the means of numerical variables, we conducted the Student's t-test or one-way ANOVA test. P < 0.05 was regarded as statistically significant.

Expression Profiles of tRNA-Derived Fragments
Differentially expressed tsRNAs were provided in Supplementary Tables 1 and 2. We performed hierarchical clustering for tsRNAs differential expression data in high-throughput sequencing files. The results indicated that tsRNAs were significantly differentially expressed between gastric cancer and non-tumor adjacent tissue specimens (NATs) ( Figure 1A). The result of PCA analysis shows a distinguishable tRF & tiRNA expression profiling among the GC and NATs samples. The figure is an overview of samples correlations using the R scatterplot3d package ( Figure 1B). In terms of the results of the scatter plot, 142 up-regulated tRFs & tiRNAs, 150 downregulated tRFs & tiRNAs, and 96 not differential expressed tRFs & tiRNAs were screened out. The Pearson correlation between GC and NATs was 0.871 ( Figure 1C). The volcano plot is based on CPM values of tsRNAs, and we found that 69 up-regulated tRFs & tiRNAs, 42 down-regulated tRFs & tiRNAs, and 277 not differential tRFs & tiRNAs were uncovered, which was taken into analysis with the criteria of the p-value (<0.05) ( Figure 1D).

GO and KEGG Analysis
We   Figure 2D). We then searched TCGA and GEO databases to compare the bioinformatic analysis with present sequencing data, and we discovered that proliferation-related pathways were significantly enriched in KEGG analysis ( Figures 2E, F). Meanwhile, the G2M checkpoint and p53 pathway in the GEO database ( Figures 2G, H), DNA replication and cell cycle pathway in the TCGA database ( Figures 2I, J) were significantly enriched in GSEA analysis. Above all, the MAPK signaling pathway was directly selected according to the bioinformatic analysis and the following biological assays of tRF-Glu-TTC-027. The Expression of tRF-Glu-TTC-027 Was

Down-Regulated in GC Significantly
We used the gel electrophoresis to further clarify the PCR product for tRF-Glu-TTC-027 ( Figure 3A). The results of Sanger sequencing confirmed the validity of the primers and the authenticity of the PCR product sequence of the tRF-Glu-TTC-027 ( Figure 3B). Next, we evaluated 35 pairs of tissues with RT-PCR, and tRF-Glu-TTC-027 was tested a low expression of great significance in GC compared with NATs, and so is in the detection of GC cells (NCI-N87, HGC-27) compared with GES-1 ( Figures 3C, D). FISH assay confirmed that tRF-Glu-TTC-027 was most concentrated in the cytoplasm ( Figure 3E). Meanwhile, designed tRF-Glu-TTC-027 mimics were capable of efficiently up-regulating the expression of tRF-Glu-TTC-027 ( Figure 3F). Subsequently, we uncovered that the expression level of tRF-Glu-TTC-027 was significantly associated with tumor size and histological grade in terms of clinicopathological studies ( Table 3). Through the analysis of the PCR data of 35 pairs of GC tissues and the follow-up data of corresponding patients, we found that tRF-Glu-TTC-027 was not significantly related to the prognosis of GC patients ( Figure 3G).  Figures 4A, B). In addition, tRF-Glu-TTC-027 was capable of suppressing the migration and invasion capacities of GC cell lines ( Figures 4C-E). Then the wound healing assay was applied to further demonstrate the effect of tRF-Glu-TTC-027 and p38 MAPK-IN on the GC cells, and the result was consistent with the previous assays ( Figures 4F, G). Moreover, EdU assays also showed that tRF-Glu-TTC-027 and p38 MAPK-IN formed less DNA replication level than the control group, which was reflected in the aspect of the fluorescence concentration of EdU ( Figures 4H, I). To differentiate and analyze the impact of tRF-Glu-TTC-027 on the GC cell cycle, we transfected cells with tRF-Glu-TTC-027 mimics, mimics control, or p38 MAPK-IN and tested the distribution of cell cycle with flow cytometry. Compared with the mimics control group, the ratio in the S phase of the tRF-Glu-TTC-027 mimics group significantly increased from 19 Figures 4J-L). Therefore  (Figures 5A, B). We demonstrated that tRF-Glu-TTC-027 inhibitor could promote the DNA replication in GC cell lines, while p38 MAPK-IN significantly suppressed the EdU assimilation and could reverse the stimulative effect of tRF-Glu-TTC-027 inhibitor during the proliferative process in EdU assay ( Figures 5C-F). Then flow cytometry was used to analyze the cell cycle, and we found that p38 MAPK-IN imposed the inhibitory effect on the GC cells to cause the cell cycle arrest and this was able to be relieved by tRF-Glu-TTC-027 inhibitor (Figures 5G-I).

tRF-Glu-TTC-027 Influenced the Expression of Related Proteins in the MAPK Signaling Pathway
To figure out the specific proteins influenced by tRF-Glu-TTC-027, we adopted immunoblotting to test the expression levels of proteins in the MAPK signaling pathway. And we found that tRF-Glu-TTC-027 inhibitor could upregulate the expression of p-p38 and c-Myc in HGC-27, and p-ERK, p-p38, and c-Myc in NCI-N87. p38 MAPK-IN could suppress the expression of p-ERK, p-p38, Elk1, p-Elk1, c-Myc, cyclinD1 in HGC-27 and NCI-N87 (Figures 6A, B). tRF-Glu-TTC-027 mimics could inhibit the expression of p-ERK, p-JNK, p-p38, c-Myc, CDK2, p-ELK1 in NCI-N87, and p38, p-p38, c-Myc, p-ELK1 in HGC-27 ( Figure 6C). To further investigate the underlying mechanism   that tRF-Glu-TTC-027 influenced the MAPK signaling pathway, we discovered 26 possible target genes by taking the intersection of tRF-Glu-TTC-027 target genes and genes in the MAPK signaling pathway ( Figure 7A). Then we analyzed the TCGA database and the Kaplan Meier plotter website to screen the significant targets. TGFB2 and ELK4 were selected as their 3' UTR owned the target sites with tRF-Glu-TTC-027 ( Figures 7B,  C), and were highly expressed in GC compared with NATs ( Figures 7D, E). Meanwhile, TGFB2 and ELK4 were associated with poor prognosis (Figures 7F, G). Finally, PCR and immunoblotting were conducted, and we found that TGFB2 was regulated by tRF-Glu-TTC-027 in HGC-27 and NCI-N87 ( Figures 7H, I).
tRF-Glu-TTC-027 Decreased Tumor Growth in NCI-N87 Xenografts The in vivo effect of tRF-Glu-TTC-027 was evaluated using NCI-N87 xenografts. The results showed that tRF-Glu-TTC-027 significantly reduced the capacity of the tumor growth ( Figures 8A, B). However, no significant difference was observed among these three groups concerning the bodyweight of the mice ( Figure 8C).  Figure 8D). The volume of the explant tumors in the tRF-Glu-TTC-027 agomir group was smaller than those in the NS and tRF-Glu-TTC-027 NC group at the endpoint of the experiment significantly ( Figure 8B). We then conducted the immunofluorescence assay and IHC assay for Ki67 to further confirm the proliferative activity of xenografts. As shown in Figure 8E, the fluorescence density of Ki67 decreased significantly in the tRF-Glu-TTC-027 agomir group compared with NS and tRF-Glu-TTC-027 NC group, and the result was consistent with the IHC assay.

DISCUSSION
tsRNAs are derived from the family of non-coding RNAs and are widely present in the biological process (8). They are involved in the cell cycle, proliferation, cell apoptosis, and many other biological regulation pathways (15). Many pieces of literature reported that tRFs are actively derived from precursor RNAs and the 3' or 5' end-matching tRFs are largely cleaved by Dicer1 owing to their structural features (7,16). Meanwhile, considering the bind method between tRFs and mRNA of the target genes, Kuscu et al. showed that Dicer-independent tRF-3s could suppress the posttranscription of genes by an Argonaute-RISC method, which had a certain degree of similarity with miRNAs (17). In addition, abnormally expressed tsRNAs can act as tumor suppressor genes or oncogenes in carcinoma through multivariate mechanisms to regulate the progression of carcinomas (11,12,18,19). Several studies have found that tRFs can regulate the activity of kinases to promote the proliferation of cancer cells (13,20). Although the roles of tRFs have been demonstrated in many kinds of tumors, GC was rarely involved. In this study, high-throughput sequencing was conducted in six pairs of GC tissues. Furthermore, 69 up-regulated and 42 down-regulated tsRNAs were discovered successfully. By expanding the amount of GC tissues to conduct the RT-PCR analysis, we selected tRF-Glu-TTC-027 as the research target. Meanwhile, bioinformatic analysis was applied to uncover the potential pathway that was able to best explain the biological characteristics of GC cell lines after the transfection of tRF-Glu-TTC-027 mimics. Interestingly, the MAPK signaling pathway successfully attracted our attention after the analysis of GO and KEGG databases. We then postulated that tRF-Glu-TTC-027 might regulate the progression of GC with the MAPK signaling pathway. Next, assays in vitro and in vivo were undertaken to demonstrate this hypothesis. We then conducted the analysis of RT-PCR results and confirmed that tRF-Glu-TTC-027 was significantly associated with histological grade and tumor size of GC. The Sanger sequencing and the gel electrophoresis were used to confirm the sequence of tRF-Glu-TTC-027. Subsequently, we used the FISH assay to demonstrate that tRF-Glu-TTC-027 was mainly distributed in the cytoplasm. Afterward, further exploration indicated that tRF-Glu-TTC-027 could significantly suppress the advancement of GC in vitro and in vivo. It should be pointed out that tRF-Glu-TTC-027 could significantly regulate the relevant proteins in the MAPK signaling pathway which exerted an influence on the oncology characteristics of GC cell lines to some extent. Hence, these findings revealed a remarkable function of tRF-Glu-TTC-027 as a tumor suppressor in GC. In summary, these results were consistent with our hypothesis that tRF-Glu-TTC-027 regulated the progression of GC with the MAPK signaling pathway.
Compared with our results, a considerable amount of studies were consistent with the present research concerning the function of tsRNAs. Recent studies discovered that tsRNAs are related to some kinds of tumors (21)(22)(23)(24). Mo et al. uncovered that 5-tiRNA Val was able to act as an inhibitor in breast cancer (12). Analogously, a novel class of tRFs influenced the YBX1 UTRs by regulating the stability of multiple oncogenic transcripts (6). Falconi reported that tRF3E could inhibit breast cancer via the NCL-mediated mechanism (11). However, some studies also reported several contrary results in terms of the biological characteristics of tsRNAs. Zhang et al. unfolded that tRF-03357 might promote the progression of HGSOC by regulating HMBOX1 (13). Huang et al. elaborated that miR-1280 was influenced by tRFs in the cancer stem-like cells via the Notch signaling pathway in colorectal cancer (19). Our present study screened the MAPK signaling pathway by bioinformatic analysis, and this was further confirmed by immunoblotting. Analogously, some other pathways, related to tsRNAs, had also been reported by a few studies (25,26). With regard to the MAPK signaling pathway, it has been uncovered and widely accepted as a pathway that could promote the progression of tumors (27)(28)(29)(30)(31). And during the process of this research, we verified that all the three classical pathways of the MAPK pathway including ERK1/2, JNK, p38 were regulated by tRF-Glu-TTC-027 to varying degrees. Interestingly, we did not find a significant correlation between tRF-Glu-TTC-027 and the prognosis of GC patients in this study. It might result from the deficiency of the GC specimens.
In this study, we applied high-throughput sequencing to discover novel diagnostic and therapeutic targets for GC, and tRF-Glu-TTC-027 was preliminarily explored. However, the further mechanism tRF-Glu-TTC-027 was involved in needs to be investigated thoroughly. For instance, the relationship between tRF-Glu-TTC-027 and TGFB2 needs to be further explored in the subsequent research. Moreover, whether the biological characteristics were only regulated by tRF-Glu-TTC-027 or not should be figured out using multiple methods. Meanwhile, the findings in this study have not fully elucidated the effects of other signaling pathways which were demonstrated to promote the progression of GC.
In summary, our study firstly elaborated the function of tRF-Glu-TTC-027 in GC. The results indicated that tRF-Glu-TTC-027 was significantly down-regulated in GC and associated with histological grade and tumor size in the aspect of pathology analysis. Furthermore, we identified that tRF-Glu-TTC-027 could suppress the progression of GC through inhibition of the MAPK signaling pathway. Taken together, tRF-Glu-TTC-027 could be a potential target for molecular therapy in GC.

DATA AVAILABILITY STATEMENT
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding authors. And there was no significant difference among these three groups in terms of the bodyweight of the mice. (E) We then conducted the immunofluorescence assay and IHC assay for Ki67 to further confirm the proliferative activity of xenografts. The fluorescence density of Ki67 decreased significantly in the tRF-Glu-TTC-027 agomir group compared with NS and tRF-Glu-TTC-027 NC group, and the result was consistent with the IHC assay. (* # P < 0.05, Student's t-test. Scale bar = 100 µm).