Investigation of the Proteasome 26S Subunit, ATPase Family Genes as Potential Prognostic Biomarkers and Therapeutic Targets for Hepatocellular Carcinoma

Abstract

Background

Several studies suggest that Proteasome 26S Subunit, ATPase (PSMC) family genes are of great importance in tumor progression and spreading, but the study for systematic evaluation of the function of PSMC genes in hepatocellular carcinoma (HCC) is currently lacking.

Methods

The functions of PSMC genes in HCC were analyzed using multiple online databases, including the TCGA database, GEO database, HPA database, cBioPortal database, DAVID, and KEGG pathway. Experiments were later conducted to verify PSMC expression.

Results

High levels of PSMC gene expression were detected in HCC tissues and PSMCs exhibited potentially powerful abilities in diagnosing HCC patients. All PSMC proteins are expressed to varying degrees in HCC tissues and high expression of the PSMC genes lead to poor prognosis in patients with HCC. Moreover, DNA methylation involves the regulation of the expression of PSMC2 and PSMC5 in HCC, and the levels of methylation of PSMC2 or PSMC5 correlate positively with patient overall survival in HCC patients. The copy number alteration and mutation of PSMC genes were observed and related to the expression of PSMCs in HCC. Functional enrichment analysis showed that many highly co-expressed genes of PSMCs had a potential role in tumor progression and metastasis, which merited further in-depth study. Functional network analysis also suggests that the primary biological function of PSMC genes is the regulation of protein homeostasis and energy metabolism in HCC. Moreover, the expression levels of PSMCs are related to immune cell infiltrates and immunomodulatory factors in HCC.

Conclusion

Our study indicates that PSMC genes are the potential target for precision immunotherapy and novel prognostic biomarkers for HCC.

Keywords:

• Proteasome 26s Subunit
• ATPase
• PSMC
• hepatocellular carcinoma
• prognostic biomarkers
• therapeutic targets

Introduction

Primary liver cancer is a major worldwide health problem, with nearly 906,000 newly diagnosed patients annually and approximately 830,000 annual deaths.¹ Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer and accounts for the great majority of liver cancer deaths.² Due to very few early-stage symptoms, HCC is often detected at a late stage, with a subsequent poor prognosis for most patients.³ Nevertheless, a considerable proportion of patients still achieved remission and prolonged survival after treatment.⁴ Exploration of the novel indicators with an ability to improve early diagnosis and therapeutic options in HCC is therefore warranted. Currently, tumor-targeted therapies are shifting the treatment outlook for patients with HCC.⁵ An ideal therapeutic target should be highly expressed in tumor tissue and not expressed in normal, healthy tissues. However, effective molecular therapeutic targets are currently lacking, limiting the roles of molecular-targeted therapies in HCC. So, finding novel therapeutic targets is still meaningful for HCC treatment.

The 26S proteasome, an important proteasome species in eukaryotes, plays a proteolytic role in the cytoplasm and the nucleus.⁶ The Proteasome 26S Subunit, ATPase (PSMC), acts as a regulatory subunit of the 26S proteasome, identifying the degradation signal and unfolding the target protein substrate. The PSMC gene family consists of PSMC1, PSMC2, PSMC3, PSMC4, PSMC5, and PSMC6.⁷ It is widely believed that PSMC family genes have a significant role in tumor development in multiple human cancers. Previous studies showed that PSMC2 has tumor-promoting roles in diverse human cancers, such as gastric, ovarian, pancreatic, breast, and prostate cancer.^8–12 In addition, PSMC6 may also exhibit the ability to promote cancer cell growth, metastasis, and invasion in the lung.¹³ However, at the moment, systematic research on the PSMC family genes and their potential as candidate prognostic markers and immunotherapeutic targets in HCC is lacking. Among the PSMC family genes, PSMC2 has been reported to promote HCC cell proliferation and cell cycling and holds great promise as a diagnostic and therapeutic target for HCC.¹⁴ Although this study focused early on the ability of PSMC2 to evaluate the prognosis of HCC, it is still worthwhile to further explore the aberrant methylation, genetic alteration frequency, immune phenotypes, and molecular characterization of the PSMC family genes in HCC. Therefore, the systematic studies of PSMC family genes are beneficial for offering a new perspective on the biomarkers of HCC and then providing new ideas for patients’ prognosis, diagnosis, and treatment.

In the present study, we performed experiments and bioinformatics analysis to evaluate the diagnostic/prognostic/therapeutic value of PSMC family genes in HCC First, we sought to analyze the expression patterns, copy number alterations, mutations, and methylation patterns of the PSMC family genes in HCC tissues. Next, we assessed the clinical relevance of the PSMC genes and whether PSMC mRNA abundances were differentially associated with overall patient survival. We further evaluated the genes co-expressed with PSMC genes and their functional enrichment in HCC. Finally, we also assessed whether the PSMC expression levels are associated with the tumor immune cell infiltration in HCC. Our study may offer a theoretical foundation for investigating the PSMC family genes as potential diagnostic indicators, prognostic markers, and immunotherapy targets for HCC.

Materials and Methods

Public Data Acquisition

Gene expression data and patient clinicopathological information for HCC were extracted from The Cancer Genome Atlas database (TCGA, https://portal.gdc.cancer.gov/). RNA sequence data from 374 patients with HCC and 50 normal tissues were downloaded from the TCGA database. One independent microarray gene expression profiling data was downloaded from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/), containing 12 normal liver tissue samples and 12 HCC tissue samples.

Differential Expression Analysis of PSMC Genes in Normal Liver and HCC Tissues

In the TCGA-HCC cohort, we used unpaired Mann–Whitney or paired Wilcoxon non-parametric tests to compare the expression of PSMC genes in different tissues. The mRNA level expression patterns of the PSMCs in a total of 24 different types of HCC cell lines were analyzed using the Expression Atlas, a value-added gene expression database (https://www.ebi.ac.uk/gxa/home).¹⁵ After that, we evaluated the protein expression of PSMC genes in HCC tissues using the Human Protein Atlas (HPA) (https://www.proteinatlas.org/) server.¹⁶ Furthermore, the area under the Receiver operating characteristic (ROC) curve was used to evaluate the ability of PSMC genes to distinguish between HCC patients and normal controls.

Assessing the Relationship Between PSMC Expression Levels and Clinical Variables of HCC Patients

In the TCGA-HCC cohort, the HCC patients were grouped by their clinical characteristics, including pathological T stage, histological grade, and pathological stage (Edmondson-Steiner grade). Next, we observed the differential expression of PSMC genes in those patients classified by clinical features. Significance testing was done by the Kruskal–Wallis test with a post hoc Dunn’s test.

The Survival Analysis Based on PSMC Expression Levels in HCC Patients

The TCGA HCC patients were dichotomized for survival analysis based on PSMC expression levels. Using the median PSMC expression level value as the cutoff point, we divided HCC patients into two groups (high and low). Kaplan Meier estimators of survival were used to visualize the survival curves. The Log rank test was used to compare overall survival between patients in different groups. Kaplan-Meier Plotter (https://kmplot.com/), a meta-analysis-based tumor biomarker assessment website, was also used to perform the survival analysis of PSMC in HCC patients.¹⁷

Evaluation of Mutations, Copy-Number Alterations, and DNA Methylation Patterns in PSMC Genes Across HCC Patients

Gene mutation, methylation, and copy number alteration (CNA) data sets were downloaded and analyzed on the cBioPortal for Cancer Genomics platform (http://www.cbioportal.org).¹⁸ Correlations between PSMC gene mRNA expression levels and methylation degree were examined by Pearson’s correlation analysis. We examined the additional prognostic value of the methylation levels in PSMC genes for predicting HCC patient outcomes using the MethSurv online tool (https://biit.cs.ut.ee/methsurv/).¹⁹ In addition, we also assessed the relationship between CNA and PSMC gene expression using the Kruskal–Wallis test. Finally, the gene expression correlations between PSMC family members were analyzed by the use of Spearman’s rank correlation coefficient.

Functional Enrichment Analysis of the Co-Expressed Genes of PSMCs in HCC Patients

To identify the co-expressed genes of PSMCs, we used the TCGA HCC database from the cBioPortal server and the InteractiVenn online tool (http://www.interactivenn.net/) which confirmed the overlap in their co-expressed genes.²⁰ Therefore, we found 1369 common genes co-expressed with each PSMC family member and performed a deep analysis based on these co-expressed genes, including Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) enrichment analysis, by using a Database for Annotation, Visualization, and Integrated Discovery database (DAVID) function annotation tool (https://david.ncifcrf.gov).²¹ Those co-expressed genes were analyzed using GO terms that provide a context of biological process (BP), cellular component (CC), and molecular function (MF), and the signaling pathways were identified by considering both p-value and count number. P values were corrected using the False discovery rate (FDR), and FDR values ≤0.05 were considered significant.

Analysis of the Correlation Between the PSMC Expression and the Abundance of Tumor-Infiltrating Immune Cells in HCC Patients

Using TCGA RNA sequencing data for HCC patients, we investigated the relationship between the PSMC expression and the abundance of eight types of immune cell infiltrates, including T cells, T helper cells, B cells, dendritic cells (DC), CD8 T cells, neutrophils, macrophages, and Regulatory T cells (TReg). We then selected eight immunomodulators that were previously identified as the regulators of the host immune response in HCC patients, including PDCD1, CD28, CD274, IDO1, IL10, CD8A, CTLA4, and LAG3.²² Finally, we also determined the association between the PSMC expression and the abundance of seven immunomodulators in the TCGA-HCC cohort. Correlations were analyzed by P value and correlation coefficient.

RNA Extraction from HCC Tissue and Real-Time PCR

HCC tissue samples were from HCC patients, while normal liver tissue samples were adjacent non-cancerous tissue from HCC patients (normal tissue n=5 and HCC tissue n=5). These HCC patients were recruited from the Suining Central Hospital in 2022. The recruitment was approved by the institutional Ethics Committee, and each patient gave their informed consent. Our research complied with the Declaration of Helsinki. Total RNA was extracted from the samples using an RNAiso Kit and reverse transcription was performed to produce cDNA by using a cDNA synthesis kit according to the manufacturer’s recommendations. The mRNA levels of target genes and the housekeeping gene β-Actin in the tissues were examined by using an ABI PRISM 7900 Sequence Detection System. The primer sequences are listed in Supplementary Table 1.

Statistical Analysis

Statistical analyses were carried out using the statistical programming language R and two-tailed P values <0.05 were considered statistically significant. We used the R packages stats to analyze the differential gene expression. Survival analysis and ROC curve analysis were performed using the packages “survival” and “pROC”, respectively. Plots used in this manuscript were generated using the following R packages: survminer (time-to-event analyses), circlize (circular visualization plots), and ggplot2 (general plots).

Results

The mRNA and Protein Expression Levels of PSMC Genes in HCC

We used TCGA mRNA data to evaluate expression levels of PSMCs in HCC and showed that all PSMC genes are upregulated in HCC tissues compared with paired or unpaired normal liver tissues (Figure 1). We next assessed the expression levels of PSMC genes across 24 HCC cell lines. The results showed that PSMC4 was discovered to be overexpressed in most of the selected cell lines followed by PSMC3 and PSMC2 (Figure 1M). All 374 TCGA HCC subjects were grouped according to the different aetiologies, including alcohol, hepatitis B/C, alcohol combined with hepatitis B/C, non-alcoholic fatty liver disease (NAFLD), and other causes. We found no significant differences in the expression levels of PSMCs in HCC tissues between groups. In addition, no significant differences in the PSMC5 expression levels were observed within normal liver tissues and NAFLD-related HCC tissues. However, PSMCs showed a higher expression level in other HCC tissue groups compared with that in normal liver tissues (Supplementary Figure S1). We also evaluated the protein levels of PSMCs in HCC tissues. The results showed that all PSMC proteins are expressed to varying degrees in HCC tissues (Figure 2). The magnified immunohistochemical images showed that PSMCs localize in both the cytoplasm and nucleus (Supplementary Figure S2). PSMC proteins expressed at different levels may play various roles in both the initiation and progression of HCC. ROC curves were plotted to score the predictions of associations between PSMC genes and HCC, and the area under the ROC curve (AUC) was calculated. The accuracy of the diagnostic test is based on the AUC; the closer AUC is to 1, the better the test. Based on the estimated AUC values, all tests under evaluation had an acceptable overall diagnostic accuracy (>0.9), except PSMC1 for HCC (AUC: 0.772) (Supplementary Figure S3). The results showed the excellent diagnostic value of PSMC genes for HCC.

Figure 1 Differential expression analysis of PSMC1 (A), PSMC2 (B), PSMC3 (C), PSMC4 (D), PSMC5 (E), and PSMC6 (F) in HCC tissues compared to normal liver tissues in TCGA. Paired differential expression analysis of PSMC1 (G), PSMC2 (H), PSMC3 (I), PSMC4 (J), PSMC5 (K), and PSMC6 (L) in HCC tissues compared to matched normal adjacent tissues in TCGA. Expression patterns of PSMCs in different HCC cell lines (M).

Abbreviations: HCC, Hepatocellular carcinoma; PSMC, Proteasome 26S Subunit ATPase; TCGA, The Cancer Genome Atlas database.

Figure 2 Immunohistochemical analysis showing different protein expression levels of PSMC1 (A), PSMC2 (B), PSMC3 (C), PSMC4 (D), PSMC5 (E), and PSMC6 (F) in HCC tissues. All representative IHC staining images are from the HPA server.

Abbreviations: PSMC, Proteasome 26S Subunit ATPase; HCC, Hepatocellular carcinoma; IHC, Immunohistochemistry; HPA, Human Protein Atlas.

Survival Difference Between HCC Patients with High PSMC Expression and Patients with Low PSMC Expression

To assess the clinical significance of PSMCs in HCC, we examined the relationship between PSMC expression level and the clinicopathological characteristics of 374 TCGA HCC samples (Supplementary Figure S4). The results showed that PSMC4 and PSMC5 expression levels were higher in HCC patients with stage T2 than that in HCC patients with stage T1. Similarly, PSMC4 and PSMC5 expression levels in HCC patients with pathologic stage II were higher than stage I in TCGA HCC data, while PSMC1 expression levels were higher in HCC patients with pathologic stage III than that in HCC patients with stage I. We also compared HCC histologic grade with PSMC expression. The results showed that PSMC4 and PSMC5 expression levels in HCC patients with histologic grade G4 were higher than stage G1 in TCGA HCC data, while PSMC3 and PSMC4 expression levels were higher in HCC patients with histologic stage G3 than that in HCC patients with stage G1. However, there was no other significant difference in PSMC expression between different clinical stages.

For survival analysis, TCGA HCC patients were grouped into low- and high-expression categories by use of the median expression of PSMC, and survival was assessed by Log rank test. The results revealed that high PSMC1 expression was associated with decreased overall (P=0.021) (Figure 3A) and decreased disease-specific (P=0.031) (Supplementary Figure S5A) survival. Similarly, PSMC2 expression was negatively correlated with overall (P=0.032) (Figure 3B) and disease-specific (P=0.031) (Supplementary Figure S5C) survival. Neither PSMC1 nor PSMC2 expression had an association with Progress Free Interval (PFI) in this cohort (Supplementary Figure S5Band D). Expression of PSMC3 (P=0.009) (Figure 3C) or PSMC4 (P=0.031) (Figure 3D) was also negatively correlated with overall survival (OS) but had no association with disease-specific survival (DSS) and PFI (Supplementary Figure S5E–H). Moreover, PSMC5 expression was negatively correlated with both OS (P=0.015) (Figure 3E) and PFI (P=0.005) (Supplementary Figure S5J) but had no association with DSS (Supplementary Figure S5I). PSMC6 expression was inversely associated with OS (P=0.006) (Figure 3F) and DSS (P=0.044) (Supplementary Figure S5K), but not with PFI (Supplementary Figure S5L). In addition to these, Kaplan–Meier survival curves were generated using Kaplan–Meier Plotter. The results also suggested that the higher expression of all PSMCs was correlated with poor OS (Figure 3G–3L).

Figure 3 Kaplan-Meier overall survival curves in HCC from the TCGA consortium depicts; (A) PSMC1 expression; PSMC1 high versus PSMC1 low (B) PSMC2 expression; PSMC2 high versus PSMC2 low (C) PSMC3 expression; PSMC3 high versus PSMC3 low (D) PSMC4 expression; PSMC4 high versus PSMC4 low (E) PSMC5 expression; PSMC5 high versus PSMC5 low (F) PSMC6 expression; PSMC6 high versus PSMC6 low. Kaplan-Meier overall survival curves in HCC from the Kaplan-Meier Plotter depict; (G) PSMC1 expression; PSMC1 high versus PSMC1 low (H) PSMC2 expression; PSMC2 high versus PSMC2 low (I) PSMC3 expression; PSMC3 high versus PSMC3 low (D) PSMC4 expression; PSMC4 high versus PSMC4 low (J) PSMC5 expression; PSMC5 high versus PSMC5 low (K) PSMC6 expression; PSMC6 high versus PSMC6 low (L).

Abbreviations: HCC, Hepatocellular carcinoma; PSMC, Proteasome 26S Subunit ATPase; TCGA, The Cancer Genome Atlas database.

The Association of PSMC Methylation and Prognosis in Patients with HCC

We analyzed the correlation between PSMC methylation and gene expression in HCC tissues. The results showed that the methylation levels of PSMC2 (Cor: −0.145, p= 0.007) (Figure 4B) or PSMC5 (Cor: −0.156, p= 0.004) (Figure 4E) were negatively correlated with gene expression, while the alterations in PSMC1, PSMC3, PSMC4, and PSMC6 methylation were not associated with the expression of genes (Figure 4A, C, D and F). We then further found the levels of methylation of PSMC2 (P=0.00051) (Figure 4H) or PSMC5 (P=0.0026) (Figure 4K) correlated positively with the survival of patients with HCC. However, we observed strong negative correlations between methylation levels of PSMC6 (P=3.7e-5) (Figure 4L) and survival in HCC patients. Methylation levels of PSMC1, PSMC3, and PSMC4 were not associated with survival (Figure 4G–J).

Figure 4 Relationship between DNA methylation and PSMC gene expression (A–F) in HCC. Kaplan-Meier survival curves display the overall survival of HCC patients with high PSMC1 methylation compared to low PSMC1 methylation (G), high PSMC2 methylation compared to low PSMC2 methylation (H), high PSMC3 methylation compared to low PSMC3 methylation (I), high PSMC4 methylation compared to low PSMC4 methylation (J), high PSMC5 methylation compared to low PSMC5 methylation (K), and high PSMC6 methylation compared to low PSMC6 methylation (L).

Abbreviations: HCC, Hepatocellular carcinoma; PSMC, Proteasome 26S Subunit ATPase.

Frequency of PSMC Mutation and Copy Number Alterations and Its Influence on Gene Expression

The mutation and copy number alteration frequency of PSMC genes in the studies on HCC were evaluated from the cBioPortal online tool. PSMC1, PSMC2, PSMC3, PSMC4, PSMC5, and PSMC6 showed an alteration frequency of 0.7, 0.7, 0.3, 0.8, 1.6, and 0.4%, respectively (Figure 5A). We next sought to assess the relationship between gene expression and CNA, including shallow deletion, diploid, gain, and amplification. We found that HCC patients with the PSMC gene copy number gain or amplification had a higher level of PSMC expression in HCC tissues, but only a small number of patients had the PSMC gene copy number gain or amplification (Figure 5B–G). This analysis suggested that CNA may not be the primary cause for the high expression of PSMC in HCC. In addition, a certain degree of gene expression correlation existed between different PSMC family members (Figure 5H).

Figure 5 Mutation analysis report on PSMC genes in HCC patients from cBioPortal (A). Relationship between CNA and the expression levels of PSMC1 (B), PSMC2 (C), PSMC3 (D), PSMC4 (E), PSMC5 (F), and PSMC6 (G) in HCC. The gene expression correlations between PSMC family members in HCC (H).

Abbreviations: HCC, Hepatocellular carcinoma; PSMC, Proteasome 26S Subunit ATPase; CAN, Copy Number Alterations.

Functional Enrichment Analysis of the Co-Expressing Genes of PSMCs in HCC Tissues

The co-expression data of PSMCs in HCC tissues were obtained using the cBioPortal for Cancer Genomics and the most significantly co-expressed gene of each PSMC was identified. The results showed a high co-expression correlation between SLIRP and PSMC1 (Cor: 0.81, p= 4.19e-82)(Figure 6A), a high co-expression correlation between PMPCB and PSMC2(Cor: 0.59, p= 1.97e-34) (Figure 6B), a high co-expression correlation between PSMD13 and PSMC3(Cor: 0.72, p= 6.21e-58) (Figure 6C), a high co-expression correlation between TIMM50 and PSMC4(Cor: 0.71, p= 1.23e-54) (Figure 6D), a high co-expression correlation between ATP5PD and PSMC5(Cor: 0.77, p= 1.16e-70) (Figure 6E), and a high co-expression correlation between PSMA3 and PSMC6(Cor: 0.60, p= 6.08e-35) (Figure 6F). Furthermore, we compared the co-expressed genes of PSMCs in HCC tissues and identified 1369 common genes. GO and KEGG enrichment analyses were conducted based on these common genes. GO enrichment analysis revealed that the biological processes involved mainly included protein binding, transcription coactivator activity, RNA binding, and histone acetyltransferase activity (Figure 6G). The major molecular functions of these common genes were mitochondrial translation, mitochondrial ATP synthesis coupled proton transport, aerobic respiration, and proteasomal ubiquitin-independent protein catabolic process (Figure 6H). In the cellular component analysis, these common genes were mainly related to the nucleosome, nucleus, cytosol, and mitochondrial inner membrane (Figure 6I). According to KEGG pathway analysis, these common genes were mainly involved in Huntington disease, Prion disease, Parkinson disease, and Proteasome (Figure 6J).

Figure 6 Top positively co-expressed genes of PSMC1 (A), PSMC2 (B), PSMC3 (C), PSMC4 (D), PSMC5 (E), and PSMC6 (F) in HCC tissues obtained from the cBioPortal. The enriched gene ontology terms of the 1369 common co-expressed genes of PSMCs in HCC tissues: (G) biological processes, (H) molecular function, (I) cellular component, and (J) KEGG pathway.

Abbreviations: HCC, Hepatocellular carcinoma; PSMC, Proteasome 26S Subunit ATPase; KEGG, Kyoto Encyclopedia of Genes and Genomes.

The Relationship Between Immune Infiltrate and PSMC Expression in HCC Patients

Here, we aimed to assess the relationship between the PSMC expression and the abundance of eight types of immune cell infiltrates in HCC tissues. PSMC1 positively correlates with T helper cells (Cor: 0.38, p <0.001), while it negatively correlates with B cells (Cor:-0.164, p <0.01) and DC (Cor:-0.18, p <0.001) (Figure 7A). The expression levels of PSMC2 negatively correlated with T cells (Cor:-0.169, p <0.01), DC (Cor:-0.178, p <0.001), CD8 T cells (Cor:-0.221, p <0.001), and B cells (Cor:-0.235, p <0.001) (Figure 7B). Moreover, gene expression of PSMC3 negatively correlated with T helper cells (Cor:-0.14, p <0.01), B cells (Cor:-0.122, p <0.05), CD8 T cells (Cor:-0.249, p <0.001), and neutrophils (Cor:-0.24, p <0.001) (Figure 7C). PSMC4 expression was also negatively correlated with DC (Cor:-0.161, p <0.01), CD8 T cells (Cor:-0.259, p <0.001), and neutrophils (Cor:-0.278, p <0.001) (Figure 7D). Besides that, PSMC5 expression was negatively correlated with T cells (Cor:-0.174, p <0.001), T helper cells (Cor:-0.244, p <0.001), B cells (Cor:-0.177, p <0.001), TReg (Cor:-0.183, p <0.001), CD8 T cells (Cor:-0.271, p <0.001), neutrophils (Cor:-0.228, p <0.001), and DC (Cor:-0.151, p <0.01) (Figure 7E). PSMC6 expression was positively correlated with T helper cells (Cor: 0.368, p <0.001), but was negatively correlated with neutrophils (Cor:-0.141, p <0.01) and DC (Cor:-0.207, p <0.001) (Figure 7F). We next assessed the relationship between PSMC expression and the immunomodulatory factors in HCC tissues. The expression of PSMC1 was positively correlated with the expression of CD28 (Cor: 0.313, p <0.001), CD274 (Cor: 0.312, p <0.001), IDO1 (Cor: 0.168, p <0.01), and IL10 (Cor: 0.165, p <0.01) (Figure 7G). PSMC2 mRNA levels showed a strong positive correlation with CD28 (Cor: 0.18, p <0.001) and CD274 (Cor: 0.159, p <0.01) expression in HCC tissues (Figure 7H). PSMC3 expression also showed a significant positive correlation with PDCD1 (Cor: 0.108, p <0.05) and LAG3 expression (Cor: 0.112, p <0.05) (Figure 7I). The expression level of PSMC4 exhibited a positive correlation with that of PDCD1 (Cor: 0.203, p <0.001), CTLA4 (Cor: 0.229, p <0.001), and LAG3 (Cor: 0.174, p <0.001) (Figure 7J). There was a significant negative correlation between PSMC5 expression and CD28 expression (Cor: −0.13, p <0.05) (Figure 7K). Finally, we found that PSMC6 expression correlated positively with the expression of PDCD1 (Cor: 0.175, p <0.001), CD28 (Cor: 0.269, p <0.001), CD274 (Cor: 0.246, p <0.001), IL10 (Cor: 0.229, p <0.001), CTLA4 (Cor: 0.2, p <0.001), CD8A (Cor: 0.172, p <0.001), and IDO1 (Cor: 0.139, p <0.01) (Figure 7L).

Figure 7 Association between the PSMC expression and the infiltration levels of immune cells (A–F) in HCC tissues identified in the TCGA database. Relationship between the PSMC gene expression and the immunomodulatory factors (G–L) in HCC tissues identified in the TCGA database. *p < 0.05, **p < 0.01, and ***p < 0.001.

Abbreviations: HCC, Hepatocellular carcinoma; PSMC: Proteasome 26S Subunit ATPase; TCGA, The Cancer Genome Atlas database; ns, no significance.

Validation of the PSMC Genes Differentially Expressed Between HCC Tissue and Normal Liver Tissue

We performed external validation by downloading the full microarray dataset (GSE147888) from the GEO database. In HCC, PSMC1 (p <0.05) (Figure 8A), PSMC2 (p <0.01) (Figure 8B), PSMC3 (p <0.01) (Figure 8C), PSMC4 (p <0.001) (Figure 8D), PSMC5 (p <0.01) (Figure 8E), and PSMC6 (p <0.05) (Figure 8F) were all expressed at higher levels in tumor tissues than in adjacent normal tissues. We next conducted real-time PCR to verify the PSMC genes differentially expressed between HCC tissue and normal liver tissue. As expected, the PCR validation also showed that the expression levels of PSMC1 (p <0.01) (Figure 8G), PSMC2 (p <0.05) (Figure 8H), PSMC3 (p <0.05) (Figure 8I), PSMC4 (p <0.05) (Figure 8J), PSMC5 (p <0.05) (Figure 8K), and PSMC6 (p <0.01) (Figure 8L) in tumor tissues were significantly higher than that in normal tissues.

Figure 8 Expression pattern of the PSMC genes in HCC tissues (n = 12) and adjacent normal liver tissues (n = 12) obtained from the GSE147888 dataset: PSMC1 (A), PSMC2 (B), PSMC3 (C), PSMC4 (D), PSMC5 (E), and PSMC6 (F). Quantitative real-time PCR verification of the expression pattern of the PSMC genes in HCC tissues: PSMC1 (G), PSMC2 (H), PSMC3 (I), PSMC4 (J), PSMC5 (K), and PSMC6 (L).

Abbreviations: HCC, Hepatocellular carcinoma; PSMC, Proteasome 26S Subunit ATPase.

Discussion

No previous studies have systematically investigated the roles of PSMC family genes in HCC development. In the present study, we sought to systematically identify PSMC family genes that could play a particularly important role in the initiation and development of HCC. Our findings reveal that high PSMC gene expression is associated with tumor immune cell infiltration and poor OS in HCC patients. In addition, the DNA methylation of PSMC genes may be involved in the development of HCC. Therefore, PSMC genes can be seen as oncogenes that are critical in HCC tumorigenesis and biomarkers for rapid tumor progression and poor prognosis in HCC.

Our study found that all the expression levels of PSMCs are significantly elevated in HCC tissues compared with the normal liver tissues. As expected, the expression levels of PSMCs in HCC tissues are nearly unaffected by the HCC etiologies. Accordingly, the expression of PSMCs is of diagnostic value for HCC. All PSMC proteins were also discovered to be expressed to varying degrees in HCC tissue, suggesting that they may play a certain function in the development of HCC. Previous studies have reported that PSMCs are highly expressed in multiple types of human tumor tissues.²³ For example, PSMC4 gene expression was found to be upregulated in a wide variety of human tumor tissues, including pituitary adenomas, oral squamous cell carcinoma, laryngeal cancer, breast cancer, and prostate cancer.^24–28 Not only that, PSMCs are considered to act as oncogenes and contribute to poor prognosis in multiple cancers. A previous study reported that PSMC1 promotes the proliferation and migration of lung adenocarcinoma cells and is related to poor prognosis in patients with lung adenocarcinoma.²⁹ PSMC5 may also promote the proliferation, invasion, and metastasis of colorectal cancer and its high expression correlates with poor prognosis in colorectal cancer.³⁰ Consistent with studies in other tumor types, high expression levels of PSMCs correlated with poor prognosis and shorter survival in HCC. Additionally, some of the PSMC genes’ expression in HCC were associated with clinicopathological features including pathologic stage and histologic grade. Therefore, it is essential to explore the molecular mechanisms that regulate PSMC expression in HCC.

In general, gene methylation could inhibit or activate gene expression, and sometimes differential methylation may be a potential target for epigenetic clinical decisions in cancer therapy.³¹ In our study, we found that increased methylation of PSMC2 and PSMC5 has been associated with reduced gene expression in HCC, as has been reported for many genes. DNA methylation in the PSMC2 or PSMC5 gene body is positively correlated with the survival of patients with HCC. We thus inferred that the hypomethylation levels of PSMC2 and PSMC5 upregulate the expression of PSMC2 and PSMC5 in HCC, leading, in turn, to the very poor prognosis of patients with HCC. It is interesting to note that the PSMC6 methylation is not associated with the expression of PSMC6 in HCC, but is negatively correlated with the survival of patients with HCC. These results suggest that PSMC6 methylation may be involved in the regulatory role of PSMC6 in prognosis but not affect the expression of PSMC6 in HCC. Moreover, we also found that gene methylation is not only irrelevant to the expression of other PSMC genes in HCC but also to the roles of other PSMC genes in affecting the outcomes of patients with HCC. To our knowledge, CNA are likely to influence gene expression and are associated with various human cancers, including HCC.^32,33 Although we also found that all the PSMCs have multiple CNA, CNA of PSMCs are not sufficient to promote high expression of PSMCs in HCC. Previous studies have shown that the gene expression correlation existed between different PSMC family members in lung adenocarcinoma.³⁴ We observed the same phenomenon in HCC and the relationship between different PSMC family members needs to be explored further.

Co-expression network analysis found that SLIRP is the gene with the highest positive correlation to PSMC1 expression in HCC, which may regulate mitochondrial function and adversely affect the prognosis of head and neck squamous cell carcinomas.³⁵ PMPCB, the gene with the highest positive correlation to PSMC2 expression, is thought to be associated with HCC resistance to sorafenib treatment.³⁶ PSMD13, the most positively correlated gene with PSMC3, is considered to be a valid predictor of prognosis and therapeutic response in patients with HCC.³⁷ Co-expressed TIMM50 gene is most relevant to the PSMC4, which negatively correlates with patient prognosis in multiple cancer types, such as lung cancer and breast cancer.^38,39 ATP5PD, the most positively correlated gene with PSMC5, promotes hepatitis B virus (HBV) replication and expression and is considered to be a new biomarker for HBV-related HCC treatment.⁴⁰ Co-expressed PSMA3 gene is most relevant to the PSMC6 and its overexpression is associated with poor clinical prognosis in various malignancies, such as breast cancer and pancreatic ductal adenocarcinoma.^41,42 In this study, we found that the expression of PSMD13, TIMM50, ATP5PD, and PSMA3 revealed negative associations with the prognosis of HCC patients (Supplementary Figure S6). Because the co-expressed genes have functional relevance, these scientific shreds of evidence indicate that the PSMC family genes likely have potential roles in driving transformation from healthy liver cells to malignancies.

According to the GO enrichment analysis, the genes co-expressed with PSMC genes in HCC were mainly enriched in functional terms related to protein homeostasis and energy metabolism. In addition, KEGG pathway analysis showed enrichment of these genes in pathways related to the diseases caused by the accumulation of denatured proteins in cells. As we now know, PSMCs, an important part of the 26S proteasome, can recognize the degradation signal and unfold the target protein substrate. Our findings are in line with previous studies, which suggested that PSMCs may also play important roles in HCC development through their effects on denatured proteins in cells.

Accumulating research has shown that immunosuppression by infiltrating immune cells leads to tumor immunotolerance.⁴³ This study found that PSMC expression was related to the tumor infiltration degrees of various immune cells in HCC. In addition, multiple PSMC expression levels were closely related to immunomodulator expression, such as CD274 (commonly known as programmed death-ligand 1; PD-L1) and CTLA4. Therapeutic targeting of CTLA4 and PD-1(alias: PDCD1) constitutes the backbone of immunotherapy for solid tumors.⁴⁴ In terms of the mechanism, the interaction between PD- L1 and PD-1 results in broad dephosphorylation of T cell-activating kinases and subsequent T cell inactivation. Recently, studies in HCC have found that myeloid cells (mainly the monocyte-derived macrophages) expressed PD-L1 play a critical role in regulating the hypoxic tumor microenvironment and immune escape of HCC.^45,46 According to our results, we speculate that through this mechanism PSMCs may be involved in the regulation of the immune response in HCC. CTLA4 inhibition can lead to increased activation of naive CD4 and CD8 T cells by acting on T cell-antigen-presenting cell immune synapse. Anti-CTLA4 therapy decreases peripheral T cell clonality and increases the abundance of CD4 and CD8 T cells in patients with HCC.⁴⁷ Therefore, the development of novel drugs to target PSMCs holds promise for immunotherapy against HCC.

In summary, this study provides a general overview of the roles of PSMC gene expression in HCC prognosis by bridging information across multi-omics data. Moreover, this study benefits from a large number of included datasets to demonstrate the predictive and therapeutic potentials of PSMCs in HCC. However, there are also some deficiencies in this study. Our analysis was bridled by the retrospective nature of the data analysis and the understanding of the roles of PSMCs in the HCC development was limited due to lack of suitable in vivo and vitro experimental validation. To further validate our proposed conclusions, we have cultivated HCC cell lines, which are ready for further wet laboratory experiments.

Ethics Approval

The study was approved by the ethics committee of the Suining Central Hospital.

Disclosure

All authors report no conflicts of interest in this work.

Additional information

Funding

This work was supported by the Medical Science Program of Chengdu University of Traditional Chinese Medicine [No. YYZX2021106], the Special Research Project on Traditional Chinese Medicine of Sichuan Provincial Administration of Traditional Chinese Medicine [No. 2023MS175], and the Medical Science Program of Sichuan Province of China [No. S22028].