Advertisement

Comparison of immune profiles between hepatocellular carcinoma subtypes

  • 61 Accesses

Abstract

Immunotherapy, especially immune checkpoint inhibitors, is becoming a promising treatment for hepatocellular carcinoma (HCC). However, the response rate remains limited due to the heterogeneity of HCC samples. Molecular subtypes of HCC vary in genomic background, clinical features, and prognosis. This study aims to compare the immune profiles between HCC subtypes and find subtype-specific immune characteristics that might contribute to the prognosis and potential of immunotherapy. The immune profiles consist of immune-related genes, cytolytic activity, immune pathways, and tumor-infiltrating lymphocytes. HCC-c1 samples showed an overall higher activation level of immune genes and pathways, and this pattern was consistent in validation sets. We associated the difference in immune profiles with the activation level of cancer hallmarks and genomic mutations. There was a negative correlation between most of the metabolism pathway and immune-related pathways in HCC samples. CTNNB1/WNT signaling pathway mutation, one of the common mutations in HCC, appears to be associated with the expression of immune genes as well. These results reveal the difference of immune profiles between HCC subtypes and possible reasons and influence, which may also deepen our understanding of the carcinogenesis process.

INTRODUCTION

Primary liver cancer is one of the most common cancer and the leading cause of cancer-related death worldwide, with a steady increasing incidence and mortality. Worldwide, there are about 841,000 new diagnosed cases and 782,000 deaths annually. Hepatocellular carcinoma (HCC) is the most common type of liver cancer, accounting for 75%–85% of primary liver cancer cases (Bray et al.2018).

HCC originates from hepatocytes. Hepatocytes constitutes of liver lobules, which is the basic function unit of liver. The risk factors of HCC vary geographically. Common risk factors include hepatitis infection, alcohol abuse, aflatoxin B, and so on (Forner et al.2018) The development of HCC is closely related to chronic liver disease, with 90% of HCC developed from cirrhosis (Llovet et al.2016).

Despite metabolism function, liver has critical immune-regulatory functions. Facing amounts of microbial byproducts and antigens from intestine, liver is under an immune-suppressive state in normal physiological conditions, to avoid overreacting to these molecules. While liver is under infection or inflammatory state,liver could also recruit immune cells and activate immune systems rapidly (Guha et al.2017; Ringelhan et al.2018). The immune-suppressive state of liver is often utilized by cancer cells to avoid immune surveillance.

Early-stage HCC patients could be treated with resection, liver transplantation, or local ablative therapy. For liver transplantation, the limited liver source restricts its application. For other treatments, the recurrence rate remained high because the chronic liver disease is not cured with the cancer (El-Serag 2011). For advanced stage patients, sorafenib has been approved as first-line therapy but just prolong patients’ mean survival time for three months (Llovet et al.2008). Regorafenib and nivolumab have been approved as second-line therapy with promising efficacy (Bruix et al.2017; El-Khoueiry et al.2017) while the response rate is not desirable (~30%) and no definitive predictive biomarkers have been found (Llovet et al.2018). Nivolumab is anti-PD1 drug, which is one of the immune checkpoints. In recent years, immune checkpoint inhibitors have made great progress in treating several cancer types. The heterogeneity of tumor microenvironment may contribute to the low response rate (Pitt et al.2016). This study aims to analyze the immune profiles of HCC subtypes and identify subtype-specific immune characteristics that might contribute to the potential of immune therapy and difference in prognosis.

In recent years, the development of sequencing technology enables us to know more about the heterogeneity of HCC, from which we could also extract immune profiles. The immune profiles include the immune-related gene expression, immune-related pathway/gene sets, estimated tumor-infiltrating lymphocytes (TILs) score, and immunogenicity. The tumor immunogenicity could be evaluated with several signatures, including mutation load, neoantigen load, and cancer-germline antigen expression. The response of immune system could be measured with TILs score and cytolytic activity (CYT). In the following, we compared the immune profiles between HCC subtypes, with data from TCGA (the Cancer Genome Atlas). Immune gene expression, pathway activation, and TILs score were obtained from transcriptome data. Mutation and neoantigen information was obtained from previous studies (Charoentong et al.2017). The study provides an integral comparison of immune profiles between HCC subtypes which might be valuable to clinical application.

RESULT AND DISCUSSION

Difference of immune-related genes by subtype

Transcriptome data, mutation files, and clinical information for HCC samples were downloaded from TCGA with cBioPortal (Cerami et al.2012; Gao et al.2013). Based on transcriptome data, TCGA-HCC samples were classified into three classes according to Hoshida’s work (Hoshida et al.2009) (supplementary Fig. S1). Clinical features differed between three subtypes, as summarized in Table 1. Similar to previous studies (Hoshida et al.2009), there were less advanced tumor in class 3 (c3), higher AFP levels in class 2 (c2), and less hepatitis infection samples in class 1 (c1). Both overall survival (OS) and disease-free survival (DFS) differed between subtypes, with c3 better in OS and c2 worse in DFS (Fig. 1C).

Table 1 Clinical difference between HCC subtypes
Fig. 1
figure1

A Heatmap of immune-related genes expression in TCGA-HCC and three validation sets. The gene expression values were calculated as log2 (RSEM + 1) and scaled by row. Values deprived out of 4SD were substituted by mean ± 4SD. The column represents sample and the row represents genes. The genes were clustered by row while gene trees were not shown here. The red color represents higher expression and blue represents lower expression. Three subtypes were annotated with different colors. B Difference of cytolytic activity (CYT) between subtypes. C Prognosis difference between TCGA-HCC subtypes. OS: Overall survival; DFS: disease-free survival. D Prognosis value of CYT in TCGA-HCC samples. Patients were separated into two groups by median

Firstly, we paid attention to the expression of 386 immune-related genes. It could be identified that three subtypes showed obvious different expression of these genes (Fig. 1A). In TCGA datasets, HCC-c1 subtype presented an overall higher expression of immune-related genes. By comparing gene expression values between c1 and other samples with Wilcoxon rank sum test, 229 immune-related genes were identified as upregulated in c1 subtype (FDR < 0.1). This pattern could be observed in the three independent validation sets as well (Fig. 1A).

In HCC, CD57+ natural killer cells (NK cells) and CD8+ T cells mediate the main cytolytic attack to the tumor cells (Ringelhan et al.2018). Cytolytic activity (CYT), evaluated as the mean expression value of five genes (GZMA, PRF1, CD8A, CD8B, GZMB) (Jiang et al.2018), could be regarded as a measurement of antitumor effects. HCC-c1 samples showed higher CYT compared with the other two subtypes (Fig. 1B, p value = 1.2 × 10−8; 9.9 × 10−9). Previous study has found CYT is associated with better prognosis in some cancer types (Wakiyama et al.2018). In TCGA-HCC samples, patients with higher CYT had better prognosis in both OS and DFS (Fig. 1D), even after adjusted to stage (OS: p value = 0.026; DFS: p value = 0.0034). The prognostic value of CYT reached agreement with the previous ideas that the immune cells preserved part of the function even in the advanced tumor site (Sanmamed and Chen 2018).

Signature genes for each subtype were identified among the 386 immune-related genes. In TCGA-HCC dataset, 229 immune-related genes expressed significantly higher in c1 compared with the other two subtypes (Wilcoxon rank sum test, FDR < 0.1) while for c2 and c3 samples, 13 and 23 immune-related genes were over-expressed, respectively. Pathway overrepresentation analyses were applied to signature genes for each subtype, and the results are summarized in supplementary Table S1. C1 over-expressed genes were enriched in antigen processing and presentation pathway (hsa04612), T cell receptor signaling pathway (hsa04660), and Th1 and Th2 cell differentiation (hsa04658).

Interferon gamma (IFN-γ) is the signature cytokine for Th1 cells (Rengarajan et al.2000), which also plays an crucial role in the tumor immune surveillance. Recent studies find that IFN-γ plays dual roles in microenvironment. It could activate antigen presentation, thus enhancing immunogenicity of tumor cells (Saha et al.2010). In contrast, it also regulates the expression of immune checkpoint genes, such as PD-L1, CTLA4, and IDO1, which may lower immune response by effector T cells (Mojic et al.2017). In TCGA-HCC samples, the expression of IFN-γ is upregulated in c1 (supplementary Fig. S2A) and positively correlated with the expression of PD-L1 (cor = 0.47), CTLA4 (cor = 0.71), and CYT (cor = 0.82) and the activation of pathway hsa04612 (cor = 0.73) (supplementary Fig. S2B–2E). After all, the differential expression of IFN-γ between subtypes plays critical role in the difference of immune profiles.

Immune checkpoint inhibitors targeting PD1, PD-L1, and CTLA4 have achieved great success in several cancer types. And the expression of PD-L1 is considered as a potential biomarker for anti-PD1 drugs (Ocker 2018). C1 subtype showed higher expression of all these three genes and it was consistent in most of the validation set except PD-L1 in GSE36376 (Fig. 2). An IFN-γ-related signature gene was used as a potential predictive marker for anti PD-1 drug pembrolizumab (Ayers et al.2017). The 18 signature genes showed higher expression in c1 samples as well (supplementary Fig. S3). Considering the higher expression of IFN-γ signature genes and PD-L1, the c1 subtype may have the greater potential to benefit from immune checkpoint inhibitors.

Fig. 2
figure2

Expression difference of immune checkpoints between subtypes. The p value calculated with Wilcoxon rank sum test was marked in the figure. Only significant results (p value > 0.05) were shown here. Outliers were removed from the boxplot. A PD1: programmed death 1; B PDL1: CD274 molecule; C CTLA4: cytotoxic T-lymphocyte associated protein 4

For over-expressed genes in c2 and c3 subtypes, we focused on the genes whose corresponding receptors were over-expressed in the same class. For c2 samples, cytokine encoding genes, BMP4, NODAL, and their corresponding receptors, BMPR1A, and ACVR2B were upregulated (supplementary Fig. S4A). For c3 samples, NRG1 and their receptors ERBB2 showed higher expression values (supplementary Fig. S4B). Both BMP4 (bone morphogenetic protein 4) and NODAL encode ligand of the TGF-β superfamily. Recent studies revealed that BMP4 could enhance HCC proliferation and metastasis (Ma et al.2017; Zeng et al.2017) and is associated with poor prognosis in HCC samples (Guo et al.2012). Over-expression of NODAL is involved in promoting invasive phenotypes of tumor cells in vitro (Duan et al.2015; Quail et al.2014). The over-expression of BMP4 and NODAL might contribute the poorer DFS of c2 samples.

Difference of TILs between subtypes

The tumor-infiltrating lymphocyte (TIL) scores were estimated using CIBERSORT (Newman et al.2015) from transcriptome data. TILs for 22 kinds of immune cells were estimated. It could be observed that in LIHC samples, 14 types of immune cells had different infiltration levels between three subtypes (Fig. 3A). C1 samples had higher infiltration level of macrophage M0, activated CD4+ memory T cells, and lower infiltration level of naïve B cell, monocytes, resting mast cells, resting CD4+ memory T cells, T follicular helper cells, and regulatory T cells. C2 samples had lower infiltration level of γδT cells. C3 samples had higher infiltration score of macrophage M2, resting dendritic cells, and lower infiltration level of activated dendritic cells.

Fig. 3
figure3

Tumor-infiltrating lymphocytes (TILs) between subtypes. A Heatmap of TILs scores. The immune cell type significantly differed between subtypes (Kruskal–Wallis test, FDR < 0.1) was marked with star. B TILs score of macrophage and monocytes between subtypes with significant level marked. The Wilcoxon rank sum test was applied. Outliers were removed from the boxplot. *p < 0.05, **p < 0.01, and ***p < 0.001. C TILs score of regulatory T cells (Tregs) between subtypes with p value marked

Among all solid organs in the body, the liver harbors the greatest proportion of macrophages, which are in term the most common infiltration immune cells in liver cancers (Robinson et al.2016). Tumor-associated liver macrophages may be derived from self-proliferation of Kupffer cells and differentiation of recruiting monocytes. In response to different signals in microenvironment, macrophages are polarized to different status and exert opposite functions. Macrophage M1, activated with IFN-γ, produces proinflammatory cytokines and chemokines. Macrophage M2, activated with IL4 and IL13, produces immune-regulatory cytokines and has phagocytic activity (Sica et al.2014). In several cancer types, infiltration level of macrophage M1 is associated with better prognosis while macrophage M2 is associated with poor prognosis (Fridman et al.2017).

From Fig. 3B, it could be observed that the TIL score of macrophage M2 is higher than macrophage M1 in every subtype, indicating a local immune-suppressive microenvironment. As stated above, c1 showed lower infiltration score of monocytes and higher infiltration of macrophage M1, consistent with higher expression level of IFN-γ in c1. C3 showed higher infiltration of macrophage M2, compared with the other two classes. When comparing the main activation signals and expressing cytokines distinguishing M1 and M2 state (Sica et al.2014), it could be found that most of the signature genes for macrophage M1, such as IL1B, TNF, STAT1, and IL6, showed elevated expression in c1. The signature genes for macrophage M2 showed less significant difference between subtypes, among which ARG1 and ARG2 were over-expressed in c3 samples (supplementary Fig. S5). ARG1 could dampen the proliferation of T cells by limiting the availability of arginine (Carambia and Herkel 2018), which may partly contribute to the lower CYT in c3 samples.

Regulatory T cells (Tregs) play an important role in establishing immune-suppressive microenvironment in tumors, impairing the activity of effector T cells. The infiltration of Tregs is associated with poor prognosis in several cancer types, including HCC. In TCGA-HCC samples, we observed that the infiltration of Tregs is associated with poor prognosis as expected (OS: HR = 2384; DFS: HR = 391.5). C1 samples show lower infiltration of Tregs than the other two classes, which might partly explain the overall higher activation level of immune genes in c1.

Difference of cancer hallmarks between subtypes

To explore the potential reasons for immune profile difference, we compared the difference of cancer hallmarks between HCC subtypes with ssGSEA (Barbie et al. 2009), as described in method. HCC subtypes showed divergent activation levels of cancer hallmarks (Fig. 4A). Consistent with immune-related gene expression pattern, c1 samples were enriched in most of the immune-related hallmarks, such as IFN-γ response, IL6-JAk-STAT3 signaling. c1 and c2 samples showed higher enrichment scores in cell cycle and MYC hallmarks, such as hallmark G2M checkpoint, E2F targets, and MYC targets. While c3 samples were enriched in metabolism-related hallmarks, such as fatty acid metabolism and bile acid metabolism, most of which were closely related to the physiological functions of liver. Considering the lower CHILD-Pugh scores in HCC-c3 samples (Table 1), it could be speculated that c3 samples may have better liver function remained, resulting in the enrichment of these metabolism pathways.

Fig. 4
figure4

A Enrichment scores (ES) of hallmarks and immune-related pathways. ES were scaled by row. The golden color represents higher ES and purple represents lower ES. Pathways were denoted as three categories based on difference enrichment pattern and major function. B Heatmap of spearman correlation efficient between ES. The row stands for immune pathways, from hallmarks and KEGG pathway. The column stands for metabolism pathways from hallmarks. C Correlation between ES of hallmark bile acid metabolism and hsa04657-IL17 signaling pathway in TCGA-HCC and two validation set, colored by subtypes. rho: spearman correlation efficient; p value: significant level of correlation

We found that the enrichment scores of immune pathways/hallmarks were negatively correlated with the metabolism-related hallmarks, except glycolysis (Fig. 4B). Hallmark glycolysis, different from other metabolism hallmarks, was enriched in c1 samples and positively correlated with immune pathways (Fig. 4B). Transferring from oxidative phosphorylation to glycolysis is one of the important metabolism reprogramming features of tumor cells, termed as “Warburg effect.” Recent studies find that during T cell activation, similar metabolism reprogramming feature could be observed (Allison et al.2017). Since we cannot distinguish metabolism profiles of different cells with bulk tumor sample, the activation of glycolysis may exert complex influence to the tumor microenvironment.

Hallmark bile acid metabolism is enriched in c3 samples and negatively correlated with most of the immune pathways/hallmarks, especially IL-17 signaling pathway (Fig. 4B, C). Similar pattern could be observed in two available validation datasets (Fig. 4C). One of the physiological functions of liver is to secret bile acids, helping fatty acids digestion and absorption. Besides its role in digestion, bile acids also exert immune-regulatory functions, probably through activation of bile acid receptors (Fiorucci et al.2010). There are two kinds of bile acid receptors in human, G-protein coupled receptors (TRG5), and nuclear receptors (FXR, CAR, PXR, etc.). FXR, also known as NR1H4, is a bile acid receptor on hepatocytes. FXR and TRG5 are expressed on circulating monocytes, macrophages, and Kupffer cells. Activation of both receptors could repress the expression of pro-inflammatory cytokines. Previous study found that treated hepatocytes with hydrophobic bile acids could upregulate the expression of IL-17A (Fiorucci et al.2018). IL-17 is a subset of cytokines important to inflammatory responses and high expression of IL-17 is related to poor prognosis in HCC samples (Zhang et al.2014).

Genomic associations with immune-related genes

Genomic background may contribute to the difference of immune profiles as well. In TCGA-HCC samples, 356 samples with the transcriptome data have the mutation files. There were 26 significantly mutated genes. The most frequent mutations were detected in TP53 (111/356), CTNNB1 (96/356), ALB (41/356), APOB (36/356), ARID1A (31/356), AXIN1 (23/356), and RB1 (20/356). TCGA-HCC subtypes showed no significant difference in mutation load and neoantigen load (supplementary Fig. S6) while the mutation frequency of four genes differed between subtypes. C1 samples have less frequent CTNNB1 mutations and c3 samples have less frequent TP53 mutations. Meanwhile, AXIN1 and RPS6KA3 are more common in c2 samples (Table 2).

Table 2 Mutation frequency difference between HCC subtypes

CTNNB1 encodes β-catenin, which binds to the product of APC gene. Both CTNNB1 and APC belong to the WNT signaling pathway. The most common mutated genes in WNT signaling pathway in TCGA-HCC include CTNNB1, AMER1 (6/356), AXIN1 (23/356), AXIN2 (6/356), and APC (10/356). If we consider patients had any one of these gene mutations as mutated in WNT signaling pathway, it could be found that frequency of WNT signaling pathway mutation varied between subtypes. In c1 samples, only 13.1% samples had mutations in WNT signaling pathway, while for c2 and c3 samples, mutated samples accounted for 46.6% and 43.8%, respectively.

Gene mutations may influence specific gene or pathway expression as well as immune-related genes. We compared whether gene mutation could significantly influence the expression of immune-related genes out of whole transcriptome. Take CTNNB1 mutation as an example, the expression of 9234 genes was correlated with CTNNB1 mutation (Wilcoxon rank sum test, FDR < 0.05), among which 240 is immune-related genes. CTNNB1 influenced more immune-related genes compared with other genes, under Fisher’s exact test (p value = 2.30 × 1010, Fig. 5A). Besides, ALB, AXIN1 and CTNNB1 mutation as well as WNT signaling pathway mutation could greatly influence the expression of immune-related gene. And most of the immune-related genes were downregulated in the CTNNB1 or WNT pathway-mutated samples (Fig. 5B; supplementary Fig. S7A). In the validation set GSE65485, 9 out of 50 tumor samples harbored CTNNB1 mutation and most of the immune-related genes were downregulated in the CTNNB1-mutated samples as well (supplementary Fig. S7B).

Fig. 5
figure5

A Percentage of genes significantly correlated with gene/pathway mutation in immune-related genes and other genes. Fisher’s exact test was performed to test for difference. CTNNB1: catenin beta 1; WNT: samples mutated in six genes were considered as mutated in WNT pathway. B Volcano plot of the differential expression of patients with and without CTNNB1 mutation. The x-axis represents the fold change (FC) of mean values between two groups, after log2-transformed. The y-axis represents the log10 FDR value calculated with Wilcoxon rank sum test. Each point represents one gene, and the significant genes (|log2(FC)| > 0.58; FDR < 0.1) were colored blue. C Percentage of genes significantly correlated with gene/pathway mutation in immune-related genes and other genes. PRAD: prostate adenocarcinoma, STAD: stomach adenocarcinoma, UCEC: uterine corpus endometrioid carcinoma

We wonder whether the negative correlation between CTNNB1 mutation/WNT pathway mutation and immune-related gene expression exists in other cancer types. According to integrative cancer genomics (IntOGen) (Gonzalez-Perez et al.2013), CTNNB1 is considered as mutational cancer driver in seven cancer types, including prostate adenocarcinoma (PRAD), hepatocarcinoma, uterine corpus endometrioid carcinoma (UCEC), stomach adenocarcinoma (STAD), colorectal adenocarcinoma (COAD), cutaneous melanoma, and medulloblastoma. Data for the former six types were collected from TCGA. Transcriptome data and mutation files were downloaded from TCGA, and similar analysis was conducted.

Similar results were found in PRAD, STAD, and UCEC. In these three cancer types, CTNNB1 mutation influenced the expression of more immune-related genes than other genes (Fig. 5C). However, the negative correlation was not observed in these three cancer types (supplementary Fig. S7C–E).

Previous research has found that WNT/β-catenin pathway could influence the cancer immunity (Pai et al.2017). These findings, though preliminary, suggest that the genomic background may influence the immune profile.

Discussion

In this study, we compared the immune profiles between HCC subtypes, searching for immune characteristic for each subtype, possible reasons, and impacts. The prognosis for HCC remains poor, and the treatment method is limited. Considering the special immunosuppressive microenvironment of liver and potential for immunotherapy, we expect that the investigation of immune profiles would deepen our understanding of carcinogenesis process and provide clues to clinical application.

C1 subtype showed a consistent higher expression of immune-related genes, CYT as well as immune checkpoints (PD-1, PD-L1,CTLA4) in TCGA data and validation sets. The higher expression of IFN-γ in c1 would increase the antigen presentation pathway meanwhile induce the expression of co-inhibitors. This would probably explain why c1 subtype didn’t show advantages in prognosis with an immune-active state.

The higher expression of PD-1 and IFN-γ proposed that c1 samples are most likely to benefit from immune checkpoint inhibitors. For c2 and c3 samples, there is possible therapy based on upregulated genes or gene mutation, listed in Table 3. ERBB3, over-expressed in c2 samples, could be the target for antibody (Gaborit et al.2016). AXIN1 mutation and RPS6KA3 mutation, with higher frequency in c2 samples, have inhibitors, respectively (Khemlina et al.2017; Schulze et al.2015). EGFR, over-expressed in c3 samples, is the target in other cancer types (Schulze et al.2015).

Table 3 Potential therapy based on signatures

For TILs, several immune cells showed different infiltration levels between subtypes, among which macrophage M1 and M2 and Tregs might play important roles in the tumor microenvironment. And the TILs were associated with prognosis as previous studies found. CIBERSORT provides a valuable estimation of TILs, while the different status of immune cells sometimes is hard to perceive. Compared with immunohistochemistry method, the location information is not available.

The difference of immune profiles was probably due to different activation level of cancer hallmarks and genomic background. It was intriguing that there was a negative correlation between most of the metabolism pathways and immune pathways. In recent years, several studies have found metabolism reprogramming is important to the functions of immune cells (Allison et al.2017; Renner et al.2017; Zhang et al. 2018). While sequencing of bulk tumor samples would not enable us to distinguish expression profiles of different cell types. Single-cell sequencing, if possible, would give us a more precise landscape of metabolism status of different cells in tumor site. However, these results may provide an overall landscape which may need further study.

Genomic background may affect the immune profile. Mutations or neoantigens generated by tumor cells may stimulate immune response. In TCGA-HCC samples, there was no significant difference of mutation/neoantigen load between subtypes. However, we observed an association between CTNNB1/WNT mutation and the expression of immune-related gene in HCC and UCEC, STAD, and PRAD. It proposed a possibility that mutations affect the immune profiles through various ways.

Besides genomic background, HCC is a disease closely related with chronic liver diseases. Different risk factors may result in different carcinogenesis process (Llovet et al.2016). In TCGA-HCC samples, several risk factors other than hepatitis infection were documented, such as alcohol consumption, non-alcohol fatty liver disease, and hemochromatosis. The frequency of these risk factors didn’t differ between subtypes. It would be interesting to identify the influence of risk factors to the immune profiles but it was not covered in this study.

DATA AND METHODS

Genomic and clinical data

Genomic and clinical data for HCC from the Cancer Genome Atlas (TCGA) were downloaded from cBioPortal, including clinical information (n = 373), RNA-sequencing expression profiles (n = 376), and mutation files (n = 366). Overall characteristic of clinical information was listed in supplementary Table S2. Mutation profiles for 26 recurrently mutated genes identified by MutSig were downloaded.

Three HCC datasets were used as validation set, listed in supplementary Table S3. Processed transcriptome data of GSE65485 and GSE36376 were downloaded from GEO (Barrett et al.2013) with the R package GEOquery (Davis and Meltzer 2007). For GSE65485 dataset, mutation status for gene TP53 and CTNNB1 was also grepped from GEO. Another dataset of paired HCC samples (Liver110) was provided from collaborators. Liver110 dataset consisted of 55 tumor samples and 55 paired normal samples acquired from surgical resection. The RNA of specimens was sequenced and the expression values of immune-related genes and classifier genes were provided from collaborators.

Subtype classification based on transcriptome

HCC samples were classified into three subtypes based on transcriptome as described in Hoshida’s paper (Hoshida et al.2009). Subtype classification was performed using gene pattern (Reich et al.2006) module nearest template prediction (Hoshida et al.2008; Reiner et al.2003; Xu et al.2008), given signature genes for each class. The confidence level of classification was evaluated with resampling, providing p value and FDR for each sample. Samples with classification FDR < 0.1 were considered as successfully classified and other samples were not included in the following analysis. Same classification procedure was applied to TCGA-HCC and three validation sets. Classification result of three validation sets was listed in supplementary Table S3.

Identification of immune-related genes

Transcriptome data of TCGA samples were downloaded from cBioPortal as RSEM values. The transcriptome data were log2-transformed before further analysis. For microarray data GSE36376, gene expression values were calculated as mean of probe detection values. The gene symbols were converted to ENTREZ ID with R package AnnotationDbi (Herve et al.2018) and org.Hs.eg.db database (Marc 2018).

The immune-related gene set was collected from TCIA and KEGG (Charoentong et al.2017; Kanehisa et al.2017). It was composed of MHC-class-related genes, immunoinhibitors, immunostimulators, cytokines, and cytokine receptors. Among them, 386 gene expressions were identified from the RNA-seq data. Genes not expressed in more than 80% of sample were removed from further analysis.

Cytolytic activity (CYT) was evaluated with the mean expression value of GZMA (granzyme A), PRF1 (perforin 1), CD8A, CD8B, and GZMB (granzyme B) referring to previous study (Jiang et al.2018).

Pathway analyses

Pathway overrepresentation enrichment test was conducted with WebGestalt (Wang et al.2017) to explicit functions of over-expressed genes for each subtype. KEGG was used as pathway database. Three hundred and eighty-six immune-related genes were used as reference set and significance level as FDR < 0.1.

Enrichment of cancer hallmarks and immune-related pathways was calculated with ssGSEA (Barbie et al.2009; Subramanian et al.2005) using R package GSVA (Hänzelmann et al.2013). Fifty hallmark gene sets were downloaded from MSigDB (Molecular Signatures Database). Twenty immune-related pathways were downloaded from KEGG.

The correlation between enrichment scores of pathways were calculated as spearman correlation. For gene expression correlation, Pearson correlation was used.

Estimation of TILs

A deconvolution method, CIBERSORT, was adopted to identify the TILs in the tumor microenvironment. With signature genes for each cell type, CIBERSORT could provide a robust estimation of the abundance of 22 immune cell types. Expression data of tumor samples were processed with the online version of the tool, with default parameter settings. The relative values of TILs were used in the following analysis.

Neoantigen and mutation load

The neoantigen information of TCGA-HCC was downloaded from TCIA (https://tcia.at/). Neoantigen load, similar as mutation load, counts the number of possible neoantigens per sample.

Statistical analyses

All statistical analyses were completed in R (R Core Team 2017).

To test the difference of clinical data between subtypes, continuous and categorical variables were tested with Kruskal–Wallis test and Fisher’s exact test, respectively.

To test differential gene expression and TILs score between subtypes, the non-parametric Kruskal–Wallis test was used. For comparison between two groups, the non-parametric Wilcoxon rank sum test was used. The p values were adjusted for multiple testing using the Benjamini–Hochberg approach.

Fisher’s exact test was used to identify whether mutation of specific genes/pathways have greater influence to immune-related genes compared with other genes. Genes significantly differently expressed between mutant and non-mutant groups were considered as influenced by the mutation.

Survival analysis

To evaluate the influence of one variable on survival, such as gene expression or TIL score, univariate cox model was used. The cox model was adjusted to stage where specified. To compare the survival difference between groups, log-rank test was used. Survival analysis was conducted in R with the package survival.

For TCGA-HCC samples, two samples who had received neoadjuvant treatment were excluded from the survival analysis.

References

  1. Allison KE, Coomber BL, Bridle BW (2017) Metabolic reprogramming in the tumour microenvironment: a hallmark shared by cancer cells and T lymphocytes. Immunology 152:175–184

  2. Ayers M, Lunceford J, Nebozhyn M, Murphy E, Loboda A, Kaufman DR, Albright A, Cheng JD, Kang SP, Shankaran V, Piha-Paul SA, Yearley J, Seiwert TY, Ribas A, McClanahan TK (2017) IFN-gamma-related mRNA profile predicts clinical response to PD-1 blockade. J Clin Invest 127:2930–2940

  3. Barbie DA, Tamayo P, Boehm JS, Kim SY, Moody SE, Dunn IF, Schinzel AC, Sandy P, Meylan E, Scholl C, Frohling S, Chan EM, Sos ML, Michel K, Mermel C, Silver SJ, Weir BA, Reiling JH, Sheng Q, Gupta PB, Wadlow RC, Le H, Hoersch S, Wittner BS, Ramaswamy S, Livingston DM, Sabatini DM, Meyerson M, Thomas RK, Lander ES, Mesirov JP, Root DE, Gilliland DG, Jacks T, Hahn WC (2009) Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1. Nature 462:108–112

  4. Barrett T, Wilhite SE, Ledoux P, Evangelista C, Kim IF, Tomashevsky M, Marshall KA, Phillippy KH, Sherman PM, Holko M, Yefanov A, Lee H, Zhang N, Robertson CL, Serova N, Davis S, Soboleva A (2013) NCBI GEO: archive for functional genomics data sets—update. Nucleic Acids Res. 41(D1):D991–D995

  5. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A (2018) Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 68:394–424

  6. Bruix J, Qin S, Merle P, Granito A, Huang Y-H, Bodoky G, Pracht M, Yokosuka O, Rosmorduc O, Breder V, Gerolami R, Masi G, Ross PJ, Song T, Bronowicki J-P, Ollivier-Hourmand I, Kudo M, Cheng A-L, Llovet JM, Finn RS, LeBerre MA, Baumhauer A, Meinhardt G, Han G, Investigators RESORCE (2017) Regorafenib for patients with hepatocellular carcinoma who progressed on sorafenib treatment (RESORCE): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet (Lond, Engl) 389:56–66

  7. Carambia A, Herkel J (2018) Dietary and metabolic modulators of hepatic immunity. Semin Immunopathol 40:175–188

  8. Cerami E, Gao J, Dogrusoz U, Gross BE, Sumer SO, Aksoy BA, Jacobsen A, Byrne CJ, Heuer ML, Larsson E, Antipin Y, Reva B, Goldberg AP, Sander C, Schultz N (2012) The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. Cancer Discov 2:401–404

  9. Charoentong P, Finotello F, Angelova M, Mayer C, Efremova M, Rieder D, Hackl H, Trajanoski Z (2017) Pan-cancer immunogenomic analyses reveal genotype-immunophenotype relationships and predictors of response to checkpoint blockade. Cell Rep 18:248–262

  10. Davis S, Meltzer PS (2007) GEOquery: a bridge between the gene expression omnibus (GEO) and bioconductor. Bioinformatics 23:1846–1847

  11. Duan W, Li R, Ma J, Lei J, Xu Q, Jiang Z, Nan L, Li X, Wang Z, Huo X, Han L, Wu Z, Wu E, Ma Q (2015) Overexpression of Nodal induces a metastatic phenotype in pancreatic cancer cells via the Smad2/3 pathway. Oncotarget 6:1490–1506

  12. El-Khoueiry AB, Sangro B, Yau T, Crocenzi TS, Kudo M, Hsu C, Kim T-Y, Choo S-P, Trojan J, Welling THR, Meyer T, Kang Y-K, Yeo W, Chopra A, Anderson J, Dela Cruz C, Lang L, Neely J, Tang H, Dastani HB, Melero I (2017) Nivolumab in patients with advanced hepatocellular carcinoma (CheckMate 040): an open-label, non-comparative, phase 1/2 dose escalation and expansion trial. Lancet (Lond, Engl) 389:2492–2502

  13. El-Serag HB (2011) Current concepts hepatocellular carcinoma. N Engl J Med 365:1118–1127

  14. Fiorucci S, Cipriani S, Mencarelli A, Renga B, Distrutti E, Baldelli F (2010) Counter-regulatory role of bile acid activated receptors in immunity and inflammation. Curr Mol Med 10:579–595

  15. Fiorucci S, Biagioli M, Zampella A, Distrutti E (2018) Bile acids activated receptors regulate innate immunity. Front Immunol 9:1853

  16. Forner A, Reig M, Bruix J (2018) Hepatocellular carcinoma. Lancet (Lond, Engl) 391:1301–1314

  17. Fridman WH, Zitvogel L, Sautes-Fridman C, Kroemer G (2017) The immune contexture in cancer prognosis and treatment. Nat Rev Clin Oncol 14:717–734

  18. Gaborit N, Lindzen M, Yarden Y (2016) Emerging anti-cancer antibodies and combination therapies targeting HER3/ERBB3. Hum Vaccin Immunother 12:576–592

  19. Gao J, Aksoy BA, Dogrusoz U, Dresdner G, Gross B, Sumer SO, Sun Y, Jacobsen A, Sinha R, Larsson E, Cerami E, Sander C, Schultz N (2013) Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal. Sci Signal 6(269):pl1

  20. Gonzalez-Perez A, Perez-Llamas C, Deu-Pons J, Tamborero D, Schroeder MP, Jene-Sanz A, Santos A, Lopez-Bigas N (2013) IntOGen-mutations identifies cancer drivers across tumor types. Nat Methods 10:1081–1082

  21. Guha P, Reha J, Katz SC (2017) Immunosuppression in liver tumors: opening the portal to effective immunotherapy. Cancer Gene Ther 24:114–120

  22. Guo X, Xiong L, Zou L, Zhao J (2012) Upregulation of bone morphogenetic protein 4 is associated with poor prognosis in patients with hepatocellular carcinoma. Pathol Oncol Res 18:635–640

  23. Hänzelmann S, Castelo R, Guinney J (2013) GSVA: gene set variation analysis for microarray and RNA-Seq data. BMC Bioinform 14:7

  24. Herve P, Marc C, Seth F, Nianhua L (2018) AnnotationDbi: annotation database interface.

  25. Hoshida Y, Villanueva A, Kobayashi M, Peix J, Chiang DY, Camargo A, Gupta S, Moore J, Wrobel MJ, Lerner J, Reich M, Chan JA, Glickman JN, Ikeda K, Hashimoto M, Watanabe G, Daidone MG, Roayaie S, Schwartz M, Thung S, Salvesen HB, Gabriel S, Mazzaferro V, Bruix J, Friedman SL, Kumada H, Llovet JM, Golub TR (2008) Gene expression in fixed tissues and outcome in hepatocellular carcinoma. N Engl J Med 359:1995–2004

  26. Hoshida Y, Nijman SMB, Kobayashi M, Chan JA, Brunet J-P, Chiang DY, Villanueva A, Newell P, Ikeda K, Hashimoto M, Watanabe G, Gabriel S, Friedman SL, Kumada H, Llovet JM, Golub TR (2009) Integrative transcriptome analysis reveals common molecular subclasses of human hepatocellular carcinoma. Cancer Res 69:7385–7392

  27. Jiang P, Gu S, Pan D, Fu J, Sahu A, Hu X, Li Z, Traugh N, Bu X, Li B, Liu J, Freeman GJ, Brown MA, Wucherpfennig KW, Liu XS (2018) Signatures of T cell dysfunction and exclusion predict cancer immunotherapy response. Nat Med 24:1550–1558

  28. Kanehisa M, Furumichi M, Tanabe M, Sato Y, Morishima K (2017) KEGG: new perspectives on genomes, pathways, diseases and drugs. Nucleic Acids Res 45:D353–D361

  29. Khemlina G, Ikeda S, Kurzrock R (2017) The biology of Hepatocellular carcinoma: implications for genomic and immune therapies. Mol Cancer 16:149

  30. Llovet JM, Ricci S, Mazzaferro V, Hilgard P, Gane E, Blanc J-F, de Oliveira AC, Santoro A, Raoul J-L, Forner A, Schwartz M, Porta C, Zeuzem S, Bolondi L, Greten TF, Galle PR, Seitz J-F, Borbath I, Haussinger D, Giannaris T, Shan M, Moscovici M, Voliotis D, Bruix J, SHARP Investigators Study Group (2008) Sorafenib in advanced hepatocellular carcinoma. N Engl J Med 359:378–390

  31. Llovet JM, Zucman-Rossi J, Pikarsky E, Sangro B, Schwartz M, Sherman M, Gores G (2016) Hepatocellular carcinoma. Nat Rev Dis, Prim, p2

  32. Llovet JM, Montal R, Sia D, Finn RS (2018) Molecular therapies and precision medicine for hepatocellular carcinoma. Nat Rev Clin Oncol 15:599–616

  33. Ma J, Zeng S, Zhang Y, Deng G, Qu Y, Guo C, Yin L, Han Y, Shen H (2017) BMP4 enhances hepatocellular carcinoma proliferation by promoting cell cycle progression via ID2/CDKN1B signaling. Mol Carcinog 56:2279–2289

  34. Marc C (2018) org.Hs.eg.db: genome wide annotation for Human.

  35. Mojic M, Takeda K, Hayakawa Y (2017) The dark side of IFN-gamma: its role in promoting cancer immunoevasion. Int J Mol, Sci, p19

  36. Newman AM, Liu CL, Green MR, Gentles AJ, Feng W, Xu Y, Hoang CD, Diehn M, Alizadeh AA (2015) Robust enumeration of cell subsets from tissue expression profiles. Nat Methods 12:453

  37. Ocker M (2018) Biomarkers for hepatocellular carcinoma: what’s new on the horizon? World J Gastroenterol 24:3974–3979

  38. Pai SG, Carneiro BA, Mota JM, Costa R, Leite CA, Barroso-Sousa R, Kaplan JB, Chae YK, Giles FJ (2017) Wnt/beta-catenin pathway: modulating anticancer immune response. J Hematol Oncol 10:101

  39. Pitt JM, Vétizou M, Daillère R, Roberti MP, Yamazaki T, Routy B, Lepage P, Boneca IG, Chamaillard M, Kroemer G, Zitvogel L (2016) Resistance mechanisms to immune-checkpoint blockade in cancer: tumor-intrinsic and -extrinsic factors. Immunity 44:1255–1269

  40. Quail DF, Zhang G, Findlay SD, Hess DA, Postovit L-M (2014) Nodal promotes invasive phenotypes via a mitogen-activated protein kinase-dependent pathway. Oncogene 33:461–473

  41. R Core Team (2017) R: a language and environment for statistical computing. R Foundation for Statistical Computing. https://www.r-project.org/

  42. Reich M, Liefeld T, Gould J, Lerner J, Tamayo P, Mesirov JP (2006) GenePattern 2.0. Nat Genet 38:500–501

  43. Reiner A, Yekutieli D, Benjamini Y (2003) Identifying differentially expressed genes using false discovery rate controlling procedures. Bioinformatics 19:368–375

  44. Rengarajan J, Szabo SJ, Glimcher LH (2000) Transcriptional regulation of Th1/Th2 polarization. Immunol Today 21:479–483

  45. Renner K, Singer K, Koehl GE, Geissler EK, Peter K, Siska PJ, Kreutz M (2017) Metabolic hallmarks of tumor and immune cells in the TumorMicroenvironment. Front Immunol 8:248

  46. Ringelhan M, Pfister D, O’Connor T, Pikarsky E, Heikenwalder M (2018) The immunology of hepatocellular carcinoma. Nat Immunol 19:222–232. https://doi.org/10.1038/s41590-018-0044-z

  47. Robinson MW, Harmon C, O’Farrelly C (2016) Liver immunology and its role in inflammation and homeostasis. Cell Mol Immunol 13:267–276

  48. Saha B, Jyothi Prasanna S, Chandrasekar B, Nandi D (2010) Gene modulation and immunoregulatory roles of interferon gamma. Cytokine 50:1–14

  49. Sanmamed MF, Chen L (2018) A paradigm shift in cancer immunotherapy: from enhancement to normalization. Cell 175:313–326

  50. Schulze K, Imbeaud S, Letouze E, Alexandrov LB, Calderaro J, Rebouissou S, Couchy G, Meiller C, Shinde J, Soysouvanh F, Calatayud A-L, Pinyol R, Pelletier L, Balabaud C, Laurent A, Blanc J-F, Mazzaferro V, Calvo F, Villanueva A, Nault J-C, Bioulac-Sage P, Stratton MR, Llovet JM, Zucman-Rossi J (2015) Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets. Nat Genet 47:505–511

  51. Sica A, Invernizzi P, Mantovani A (2014) Macrophage plasticity and polarization in liver homeostasis and pathology. Hepatology 59:2034–2042

  52. Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, Gillette MA, Paulovich A, Pomeroy SL, Golub TR, Lander ES, Mesirov JP (2005) Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci USA 102:15545–15550

  53. Wakiyama H, Masuda T, Motomura Y, Hu Q, Tobo T, Eguchi H, Sakamoto K, Hirakawa M, Honda H, Mimori K (2018) Cytolytic activity (CYT) score is a prognostic biomarker reflecting host immune status in hepatocellular carcinoma (HCC). Anticancer Res 38:6631–6638

  54. Wang J, Vasaikar S, Shi Z, Greer M, Zhang B (2017) WebGestalt 2017: a more comprehensive, powerful, flexible and interactive gene set enrichment analysis toolkit. Nucleic Acids Res 45:W130–W137

  55. Xu L, Shen SS, Hoshida Y, Subramanian A, Ross K, Brunet J-P, Wagner SN, Ramaswamy S, Mesirov JP, Hynes RO (2008) Gene expression changes in an animal melanoma model correlate with aggressiveness of human melanoma metastases. Mol Cancer Res 6:760–769

  56. Zeng S, Zhang Y, Ma J, Deng G, Qu Y, Guo C, Han Y, Yin L, Cai C, Li Y, Wang G, Bonkovsky HL, Shen H (2017) BMP4 promotes metastasis of hepatocellular carcinoma by an induction of epithelial-mesenchymal transition via upregulating ID2. Cancer Lett 390:67–76

  57. Zhang X, Weng W, Xu W, Wang Y, Yu W, Tang X, Ma L, Pan Q, Wang J, Sun F (2014) Prognostic significance of interleukin 17 in cancer: a meta-analysis. Int J Clin Exp Med 7:3258–3269

  58. Zhang Q, Lou Y, Bai X-L, Liang T-B (2018) Immunometabolism: a novel perspective of liver cancer microenvironment and its influence on tumor progression. World J Gastroenterol 24:3500–3512

Download references

Acknowledgements

The results shown above are in part based upon data generated by the TCGA Research Network: https://www.cancer.gov/tcga. This work was financially supported in part by grants from the National Natural Science Foundation of China (31771472) and National Key R&D Program of China (2017YFC0907505, 2016YFC0901704, and 2017YFC0908405).

Author information

Correspondence to Hong Li or Yixue Li.

Ethics declarations

Conflict of interest

All authors declare that they have no conflict of interest.

Human and animal rights and informed consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 2430 kb)

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Pan, X., Lin, P., Feng, F. et al. Comparison of immune profiles between hepatocellular carcinoma subtypes. Biophys Rep (2020) doi:10.1007/s41048-019-00102-w

Download citation

Keywords

  • Hepatocellular carcinoma
  • Immune
  • Tumor-infiltrating lymphocytes
  • Metabolism
  • CTNNB1 mutation