Diagnostic and prognostic value of MATN3 expression in gastric carcinoma: TCGA database mining
Original Article

Diagnostic and prognostic value of MATN3 expression in gastric carcinoma: TCGA database mining

Ding Li1,2,3, Jianqiu Xu1,2,3, Xiaochen Dong1,2,3, Wenjing Chen1,2,3, Lingling Pan1,2,3, Hao Jiang1,2,3, Jingye Pan1,2,3, Yueyue Huang1,2,3

1Department of Intensive Care Unit, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China; 2Key Laboratory of Intelligent Treatment and Life Support for Critical Diseases of Zhejiang Provincial, Wenzhou, China; 3Wenzhou Key Laboratory of Critical Care and Artificial Intelligence, Wenzhou, China

Contributions: (I) Conception and design: J Pan, Y Huang; (II) Administrative support: D Li, J Xu, X Dong; (III) Provision of study materials or patients: W Chen; (IV) Collection and assembly of data: L Pan; (V) Data analysis and interpretation: H Jiang; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Dr. Yueyue Huang; Dr. Jingye Pan. Department of Intensive Care Unit, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China. Email: huangyueyue@wmu.edu.cn; wmupanjingye@126.com.

Backgrounds: Globally, the high morbidity and mortality of gastric carcinoma (GC) have been one of the great challenges facing humanity. However, the early diagnosis of GC is still unknown. Matrilin-3 (MATN3) is a member of the extracellular matrix (ECM) protein family. Previous studies have reported a correlation between the expression of MATN3 and bone disease. However, the role of MATN3 in GC has not been reported in depth, which can have a possible far-reaching implication for GC.

Methods: We explored the diagnostic and prognostic value and pathway enrichment of MATN3 expression in GC. Limma package conducted by R was used to analysis the difference expression data of MATN3 from The Cancer Genome Atlas (TCGA). The receiver operating characteristic (ROC) curve analysis was used to estimate the diagnostic value of MATN3 expression. univariate and multivariate analysis were used to assess the prognostic value of MATN3, and gene set enrichment analysis (GSEA) to identify the enriched signaling pathways.

Results: MATN3 was found to be significantly higher in GC tissue samples. GC patients with high MATN3 expression had poor prognosis. Then, GSEA showed that the gene sets were correlated with signaling pathways including ECM receptor interaction, hypertrophic cardiomyopathy (HCM), and glycosaminoglycan biosynthesis chondroitin sulfate, among others.

Conclusions: The study suggests that MATN3 can serve as a potential diagnostic and prognostic biomarker for GC.

Keywords: Diagnosis; prognostic; matrilin-3 (MATN3); gastric carcinoma (GC)

Submitted Apr 22, 2021. Accepted for publication Jun 11, 2021.

doi: 10.21037/jgo-21-267

Introduction

GC is one of the five most common cancers both in developed and developing regions and the 3rd leading cause of cancer death (1). In 2020, the number of new cases in GC was 27,600 and 11,010 estimated deaths, and the five-year survival rate was only 32% (2010–2016) (2). In developed countries, GC remains one of the leading causes of mortality cancers in the matures (3). Additionally, GC is one of the most common cancers, with morbidity and mortality rates corresponding to age in China. (4). Currently, early surgical resection results in a five-year survival rate of 85–95% in GC patients with stage I. Therefore, surgery remains the preferred treatment for GC (5). However, the feasibility of colonoscopy and serology-based prophylactic screening and the lack of obvious early manifestations restrict the early diagnosis of GC (6,7), which aggravates the proportion of GC prognosis. Consequently, early and precise diagnosis using GC biomarkers can help to the improvement of the prognosis of these patients.

The matrilin (MATN) family has 4 members. MATN3 is expressed mainly in cartilage (8) and is a new member of the extracellular matrix (ECM) protein family which have relation to the cartilage matrix protein and von Willebrand factor (9). Previous studies have reported that MATN3 was found in matrix formed by cultured chondrosarcoma cells and is involved in the development of cartilage and bone (10). Mutations in MATN3 have been associated with common skeletal diseases and rare chondrodysplasias (11). At present, MATN3 expression has rarely been reported in cancer patients and remains largely unclear. Therefore, the identification of reliable biomarkers is essential for the diagnosis and prognosis of GC.

The aim of this study was to assess the diagnostic and prognostic value of MATN3 expression in human GC based on data from the Cancer Genome Atlas (TCGA). Gene set enrichment analysis (GSEA) was used to further analyze the biological pathways of the MATN3 regulatory network associated with GC pathogenesis. We present the following article in accordance with the REMARK reporting checklist (available at https://dx.doi.org/10.21037/jgo-21-267).

Methods

RNA-sequencing data collection

The gene-sequenced expressed data included 407 cases and 32 normal samples, and the corresponding information of clinical data was downloaded from the TCGA Genome Data Commons (GDC) data portal (https://portal.gdc.cancer.gov/repository). The final RNA-Seq gene-expression data and clinical information data of 375 patients were retained and further analyzed (Table 1). The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013).

Table 1
Table 1 TCGA gastric cancer patient characteristics
Full table

GSEA

GSEA is a calculation method for determining whether an a priori definition of a set of the genes is a statistically significant and consistently different between two biological states and is designed to detect expression changes in a modest but functionally coordinated set of genes (12,13). Here, Gene expression datasets and phenotypic marker files were then generated and uploaded to GSEA the computer software. GSEA analyses were used to show the significant survival differences between the high- and low-MATN3 groups of TCGA patients. Gene alignments were performed 1,000 times for each group. Enriched pathways in each phenotype were identified by setting the nominal P value (NOM P val) <0.05 and the false discovery rate q-value (FDR q-val) <0.05.

Statistical analysis

All statistical analyzes were carried out using R (v.3.6.3). Wilcoxon signed rank test and logistic regression were used to assess the relationship between clinicopathological characteristics. Cox regression and Kaplan-Meier methods were used to analyze clinicopathological characteristics associated with overall survival (OS) in patients with TCGA. Subject work characteristic (ROC) curve analysis was performed using Wilson’s method and percentage outcomes in conjunction with the survival ROC package. The relationship between MATN3 expression and clinicopathological characteristics was analyzed using univariate logistic regression. The effect of MATN3 expression on survival was compared with other clinical characteristics (e.g., age, distant metastatic status, grading, lymph node status, staging) using univariate and multifactorial Cox analysis. The median was established as the MATN3 expression cutoff value, and patients were divided to two groups.

Results

Patient characteristics

Gene expression data for 407 patients were obtained by downloading from the TCGA website in May 2020. clinical data for 375 tumor patients was shown in Table 1. The age group of 70–79 accounted for the largest proportion (32.61%), followed by the 60–69 age group (29.38%), 50–59 age group (23.18%), >80 age group (7.82%), and <49 age group (7.01%). There were 19 cases (5.18%) in group T1, 80 cases (21.80%) in group T2, 168 cases (45.78%) in group T3 and 100 cases (27.17%) in group T4. N0 type tumors were the majority (31.09%, N=111), N1 type 27.17% [97], N2 type 21.73% [75] and N3 type 20.73% [74]. G1 GC cases accounted for 3.76% [10], G2 for 51.50% [137], and G3 for 44.74% [119]. Out of the 375 cases, 25 (7.04%) cases had distant metastasis. Two hundred and forty-one (64.27%) males and 134 females (35.73%) were composited for the gender composition.

MATN3 expression and its diagnostic value

We analyzed the MATN3 expression data from 407 samples. As Figure 1A shows, the expression of MATN3 levels were significantly correlated with tumor type (P=1.069e-11). There were also significant differences in the expression of MATN3 in tumor versus paraneoplastic tissues for 27 paired composition (Figure 1B). To assess the diagnostic efficacy of MATN3, we performed ROC curve analysis on the expression data from tumor and normal samples. The area under the ROC curve was 0.8618 [95% confidence interval (CI): 0.8216–0.9021] (Figure 1C). According to Kaplan-Meier survival analysis, those with high MATN3 expression had a poorer prognosis in 375 patients (Figure 1D, P=2.699e-04).

Figure 1 MATN3 expression level and its role in GC. (A) In the TCGA cohort, tumor patients had higher than normal levels of MATN3 expression. (B) MATN3 expression level was higher in tumor tissues than in paracancerous tissues. (C) ROC curves of MATN3 expression in normal gastric and tumor tissues. (D) Expression of MATN3 in the TCGA cohort and overall survival of gastric cancer patients. MATN3, matrilin-3; GC, gastric carcinoma; TCGA, The Cancer Genome Atlas; ROC, receiver operating characteristic.

MATN3 expression and clinicopathological parameters

Then, we analyzed the clinicopathological data of 375 GC patients from TCGA, including clinical stage (stage), age at diagnosis (age), gender, histological grade, survival status, and survival time, as well as tumor, node, and metastasis (TNM) classification. As shown in Figure 2A-G), increased MATN3 expression was found to be significantly related to staging (P=0.015) and to T staging (P=6.152e-4).

Figure 2 Association between MATN3 expression and clinicopathological characteristics, (A) gender, (B) distant metastases, (C) clinical grade, (D) age, (E) clinical stage, (F) tumor stage, (G) lymph node metastasis. MATN3, matrilin-3.

MATN3 expression was characterized as a classified dependent variable with poor prognosis of clinicopathology, confirmed by univariate logistic regression (Table 2). Increasing GC MATN3 expression was significantly associated with higher stage classification [ratio (OR) =2.679 II vs. I, OR =2.233 III vs. I, IV vs. I OR =2.353] and T type (T2 vs. T1 OR =4.363, T3 vs. T1 OR =6.154, T4 vs. T1 OR =6.261).

Table 2
Table 2 Logistic regression of MATN3 expression# and clinical pathological characteristics
Full table

Multivariate analysis

Univariate analysis showed that high MATN3 expression was substantially correlated with poor OS [hazard ratio (HR) =1.424, 95% CI: 1.200–1.689, P=5.08e-05]. Other clinicopathological variables included age, advanced stage, and TNM classification associated with poor survival (Table 3).

Table 3
Table 3 Univariate and multivariate analysis of the relationship between MATN3# expression and overall survival among gastric patients
Full table

High MATN3 expression remained independently associated with OS was analyzed by multivariate Cox (HR =1.109, 95% CI: 1.051–1.133, P=5.66e-06) and age (HR =1.440, 95% CI: 1.188–1.746, P=0.000) among GC patients (Figure 3).

Figure 3 Multivariate analysis of MATN3 expression and overall survival in patients with GC patients. MATN3, matrilin-3; GC, gastric carcinoma.

GSEA identified MATN3-related signaling pathways

Finally, we used GSEA to recognize the activated signaling pathways in GC, using the Median expression level of MATN3 to classify patients. There was a significant difference (NOM P val =0.05, FDR q-val =0.05) in the degree of the enrichment of the MsigDB collection (v:c2.cp.kegg.v7.1.symbols.gmt). As shown in Figure 4, the gene sets were related to ECM receptor interaction, hypertrophic cardiomyopathy (HCM), glycosaminoglycan biosynthesis chondroitin sulfate, focal adhesion, glycosphingolipid biosynthesis ganglio series, dilated cardiomyopathy, basal cell carcinoma, and neuroactive ligand-receptor interaction.

Figure 4 Enrichment plots from GSEA. GSEA, gene set enrichment analysis.

Discussion

MANT3, located on chromosome 2p24.1, is related to the cartilage matrix protein (matrilin-1) and von Willebrand factor (9,11). However, the role of MANT3 in human cancer has rarely been reported, especially in GC, which has prompted us to conduct further study. In this study, for the first time, we comprehensively analyzed the relationship between the mRNA profile of MANT3 and the diagnosis and prognosis of GC using multiple TCGA databases via bioinformatics and GSEA analysis.

In the present study, we found that MATN3 was significantly increased in GC tissue samples than in control and paired adjacent ones. This suggests that up-regulation of MATN3 expression may be associated with the occurrence of GC.

In addition, we examined the clinical diagnostic and prognostic value of MATN3 expression in GC patients. First, high MANT3 expression was found to be associated significantly with histological staging and T-staging. Second, Kaplan-Meier curves of OS showed that poor prognosis of gastric cancer patients was associated with high MATN3 expression. The area under the ROC curve indicated that upregulation of MATN3 expression had diagnostic value. Furthermore, univariate logistic analysis showed that MATN3 expressing correlated with clinical stage, T-type staging and other clinical outcomes. Univariate and multifactorial Cox analyses demonstrated that MATN3 expression could be a viable independent signifier of poor prognosis for patients with GC. Multifactorial Cox analysis showed that age was an independently risk factor for OS in patients with GC. Taken together, it is shown that high expression of MATN3 may be a potential diagnostic marker and a marker of poor prognosis in gastric cancer patients. MATN3 may also be a key target gene involved in the growth and metastasis of GC cells.

Furthermore, we observed that high MATN3 expression was associated with ECM receptor interaction, HCM, glycosaminoglycan biosynthesis chondroitin sulfate, focal adhesion, glycosphingolipid biosynthesis ganglio series, dilated cardiomyopathy, basal cell carcinoma, and neuroactive ligand-receptor interaction by GSEA. Previous studies have reported that ECM receptor interaction may be associated with breast cancer (14,15). HCM also causes more deaths and mortality (16). Glycosaminoglycan sulfate may play a role in lung fibrosis in certain cancer patients (17). Focal adhesion has been reported as an independent factor in cell migration, which is key to cancer dissemination (18).Guri et al. (19) have reported that glycosphingolipid promotes tumorigenesis in hepatocellular carcinoma (HCC). Dilated cardiomyopathy is a clinical diagnosis which can lead to fatal arrhythmias (20,21). Basal cell carcinoma is the single most frequent malignancy, and its occurrence is on the rise (22). Studies also demonstrated that neuroactive ligand-receptor interaction is related to GC (23) and glioblastoma (24). Two of the pathways listed above were not associated with cancer, but those linked to heart disease were associated with higher death rates.

Predicting protein function from mRNA is useful in some ways but not perfect (25). In our study, the association between MATN3 protein with MATN3 mRNA expression was not verified. Because of this, experiments and local clinical information will be conducted in the future.

In summary, MATN3 expressed could be a possible diagnostic and prognostic indicator of low survival in GC. Moreover, ECM receptor interaction, HCM, glycosaminoglycan biosynthesis chondroitin sulfate, focal adhesion, glycosphingolipid biosynthesis ganglio series, dilated cardiomyopathy, basal cell carcinoma, and neuroactive ligand-receptor interaction may be the pathways regulated by MANT3 in GC. Further studies should be conducted to confirm the biological impact of MATN3 expression.

Acknowledgments

Thank you to the anonymous reviewers for their valuable comments and suggestions that helped improve the quality of our manuscript. We would like to express our most sincere thanks to TCGA for providing data support.

Funding: The study was supported by the National Natural Science Foundation of China (81873949, 81671968), Medical Innovation Discipline of Zhejiang Province (Critical Care Medicine, Y2015), Major project co-founded by Zhejiang Province and Ministry of Science and Technology (WKJ-ZJ-1909), Major Science and Technology Project of Wenzhou Science and Technology Bureau (2018ZY002), Applied Research Fund of Wenzhou Science and Technology Bureau (ZG2020012), and Research of Emergency Project on Prevention and Control for COVID-19 of Wenzhou Science and Technology Bureau (ZY202001-2).

Footnote

Reporting Checklist: The authors have completed the REMARK reporting checklist. Available at https://dx.doi.org/10.21037/jgo-21-267

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://dx.doi.org/10.21037/jgo-21-267). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). Institutional ethical approval and informed consent were waived.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.

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(English Language Editor: C. Betlazar-Maseh)

Cite this article as: Li D, Xu J, Dong X, Chen W, Pan L, Jiang H, Pan J, Huang Y. Diagnostic and prognostic value of MATN3 expression in gastric carcinoma: TCGA database mining. J Gastrointest Oncol 2021;12(4):1374-1383. doi: 10.21037/jgo-21-267

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