The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer

Huang, Runzhi; Zhang, Jiaqi; Li, Mingxiao; Yan, Penghui; Yin, Huabin; Zhai, Suna; Zhu, Xiaolong; Hu, Peng; Zhang, Jiaxin; Huang, Ling; Li, Man; Sun, Zehui; Meng, Tong; Yang, Daoke; Huang, Zongqiang

doi:https://doi.org/10.1155/2020/6527564

PPAR Research

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Abstract Introduction Materials and Methods Results Discussion Conclusion Data Availability Ethical Approval Disclosure Conflicts of Interest Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

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Volume 2020 | Article ID 6527564 | https://doi.org/10.1155/2020/6527564

The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer

Runzhi Huang,^1,2,3Jiaqi Zhang,¹Mingxiao Li,¹Penghui Yan,¹Huabin Yin,⁴Suna Zhai,⁵Xiaolong Zhu,¹Peng Hu,¹Jiaxin Zhang,¹Ling Huang,¹Man Li,¹and Zehui Sun¹ et al.

Academic Editor: Sainan Li

Received30 Jun 2020

Revised21 Jul 2020

Accepted31 Jul 2020

Published22 Sept 2020

Abstract

Peroxisome proliferator-activated receptors (PPARs) are members of nuclear transcription factors. The functions of the PPAR family (PPARA, PPARD, and PPARG) and their coactivators (PPARGC1A and PPARGC1B) in maintenance of lipid and glucose homeostasis have been unveiled. However, the roles of PPARs in cancer development remain elusive. In this work, we made use of 11,057 samples across 33 TCGA tumor types to analyze the relationship between PPAR transcriptional expression and tumorigenesis as well as drug sensitivity. We performed multidimensional analyses on PPARA, PPARG, PPARD, PPARGC1A, and PPARGC1B, including differential expression analysis in pan-cancer, immune subtype analysis, clinical analysis, tumor purity analysis, stemness correlation analysis, and drug responses. PPARs and their coactivators expressed differently in different types of cancers, in different immune subtypes. This analysis reveals various expression patterns of the PPAR family at a level of pan-cancer and provides new clues for the therapeutic strategies of cancer.

1. Introduction

Peroxisome proliferator-activated receptors (PPARs), members of nuclear receptor subfamily, are a series of ligand-activated transcription factors (TFs) that regulate the expression of target genes, which involve in various biological processes, including cellular differentiation, cell proliferation, lipid metabolism, and tumorigenesis [1]. PPARs can be activated by various ligands, such as fatty acids (FAs), eicosanoids, and some targeted drugs [2]. Upon binding to the ligand, PPARs form a heterodimer with retinoid X receptor (RXR), and this PPAR/RXR complex is required for its subsequent binding to specific DNA regions in PPAR response elements (PPREs), the gene promotor region [3]. PPARs then trigger transcription of target genes after recruitment of coactivators and release of corepressors [4]. PPARGC1A and PPARGC1B were peroxisome proliferator-activated receptor gamma coactivators 1 alpha and beta, respectively, playing important roles in the PPAR signaling network [5]. There are mainly three isotypes of PPARs with distinct tissue distribution, metabolic patterns, and ligand specificity: PPARα, PPARγ, and PPARδ [6]. Although the roles of the three isotypes played in carcinogenesis and chemoprevention have not been clearly characterized [7], some agonists of them have been used in clinical trials for years. There is no conclusions but controversial results regarding the antitumor functions of PPARα and PPARγ [8]. The characteristics of PPARs differ from each other, and different isotypes may have different impacts in different types of cancer. To date, there is no bioinformatics study systematically investigating the transcriptional levels of each PPAR in pan-cancer. Thus, it is of importance to study the PPARs’ expression patterns in pan-cancer and exploit the potential of PPAR-targeted drugs when it comes to the treatment of differentially PPAR-expressed tumors.

In this study, we analyzed the expression signatures of PPARA, PPARD, PPARG, PPARGC1AA, and PPARGC1B in pan-cancer. Utilizing multidimensional correlation analysis, we found the associations between transcriptional levels of PPARs and stemness, tumor purity, and drug sensitivity across TCGA cancers.

2. Materials and Methods

2.1. Data Downloading and Preprocessing

On June 23, 2020, the gene expression profiles, phenotype information, and survival data of PARRA, PPARD, PPARG, PPARGC1A, and PPARGC1B in 33 types of TCGA tumor samples and adjacent tissues (a total of 11,057 samples) were downloaded from GDC TCGA sets in the UCSC Xena database (http://xena.ucsc.edu/) in formats of Fragments Per Kilobase per Million (FPKM) and HTSeq-Counts. Meanwhile, demographics, tumor information, and follow-up data of all patients were also extracted from the database.

The 33 types of TCGA tumors and abbreviations were as follows: adrenocortical carcinoma (ACC), Bladder Urothelial Carcinoma (BLCA), breast invasive carcinoma (BRCA), cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), Cholangiocarcinoma (CHOL), colon adenocarcinoma (COAD), Lymphoid Neoplasm Diffuse Large B-cell Lymphoma (DLBC), esophageal carcinoma (ESCA), glioblastoma multiforme (GBM), head and neck squamous cell carcinoma (HNSC), Kidney Chromophobe (KICH), kidney renal clear cell carcinoma (KIRC), kidney renal papillary cell carcinoma (KIRP), Acute Myeloid Leukemia (LAML), Brain Lower Grade Glioma (LGG), liver hepatocellular carcinoma (LIHC), lung adenocarcinoma (LUAD), lung squamous cell carcinoma (LUSC), Mesothelioma (MESO), ovarian serous cystadenocarcinoma (OV), pancreatic adenocarcinoma (PAAD), Pheochromocytoma and Paraganglioma (PCPG), prostate adenocarcinoma (PRAD), rectum adenocarcinoma (READ), Sarcoma (SARC), Skin Cutaneous Melanoma (SKCM), stomach adenocarcinoma (STAD), Testicular Germ Cell Tumors (TGCT), thyroid carcinoma (THCA), Thymoma (THYM), Uterine Corpus Endometrial Carcinoma (UCEC), Uterine Carcinosarcoma (UCS), and Uveal Melanoma (UVM) from GDC TCGA documents in the UCSC Xena database.

2.2. Differential Expression Analysis and Coexpression Analysis of PPARs between Tumor and Normal Samples

For each and across all TCGA tumor types, we used the “ggpubr” R package to perform differential expression analysis (Wilcox test) between tumor and normal tissues. Only tumor types with more than 3 normal samples were included. The differences in expression of the 5 PPAR family genes in pan-cancer were presented in a form of log2 Fold Change (log2 FC) in a heatmap.

Using corrplot R package, coexpression analysis between PPARA, PPARD, PPARG, PPARGC1B, and PPARGC2B was also done at a transcriptional level, to explore the potential expression pattern between every two PPAR genes. Moreover, a protein-protein interaction network among those genes was constructed by using the STRING database (https://string-db.org/) [9].

2.3. Clinical Correlation Analysis

To analyze the differences in overall survival outcomes between patients expressing high and low levels of PPARs, Kaplan-Meier plots for PPAR genes in pan-cancer were generated by using the R package. Phenotype and survival data for 33 TCGA cancer types were downloaded on June 23, 2020, from GDC TCGA sets in the UCSC Xena database (http://xena.ucsc.edu/). Patients were divided into high- and low- expression groups according to the median expression level of PPARA, PPARD, PPARGC1A, and PPARGC1B, respectively.

In addition, Cox proportional hazard regression was applied to access the hazard ratios of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B in each TCGA tumor type. Moreover, differential analysis was also used to detect the differences in the level of PPAR expression signatures in different stages of STAD as an example. The threshold for significance was set as two-paired .

2.4. Immune Subtype Analysis

Roles of immune tumor microenvironment (TME) were of therapeutic and prognostic significance in antitumor therapies. Six immune subtypes across TCGA tumor types had been identified by investigators based on five representative immune signatures, which offered a resource for analyzing the TME of some specific tumor. For TCGA tumors, the distribution of immune subtypes varies from each other and each immune subtype presents different biological and clinical features, which determine antitumor therapied to some extent [10]. To access the mRNA expression levels of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC2B in the six different immune subtypes across TGCA tumor types, we performed differential expression analysis with the Kruskal test. Tumors were characterized by immunogenomic features identified by Thorsson et al., including wound healing (C1), IFN-γ dominant (C2), inflammatory (C3), lymphocyte depleted (C4), immunologically quiet (C5), and TGF-β dominant (C6) [10].

2.5. Stemness Indices and TME in Pan-Cancer

More than tumor cells, solid tumor tissues consist of other normal cells, such as stromal cells, immune cells, and vascular cells, which made up TME together. We intended to analyze the correlation between PPAR expression and the fraction of stromal and immune cells in TCGA tumor samples. Methods to access the proportion of these two TME components had been proposed, one of which was ESTIMATE (Estimation of STormal and Immune cells in MAlignant Tumors using Expression data) [11]. The ESTIMATE score was calculated based on gene expression signatures and could reflect tumor purity with favorable prediction accuracy. Thus, Spearman correlation analysis was performed between the expression level of 5 PPAR genes and stromal score by using the estimate package and limma package.

To further analyze the associations between PPARs and stemness features of pan-cancer, we calculated the stemness indices of TCGA tumor samples by using a one-class logistic regression (OCLR) algorithm and performed Spearman correlation analysis based on gene expression and stemness scores [12]. Stemness indices describe the features of self-renewal and dedifferentiation within tumor cells, which might promote distant metastasis and tumorigenesis. Here, two types of stemness indices were obtained, including the DNA methylation-based stemness index (DNAss) and mRNA expression-based stemness index (RNAss).

For breast invasive carcinoma and liver hepatocellular carcinoma, specifically, we accessed RNAss, DNAss, stromal score, immune score, and ESTIMATE score (the algebraic sum of the stromal score and the immune score) to analyze the correlation relationship with PPAR transcriptional expression.

2.6. Drug Sensitivity Analysis in Pan-Cancer

The data including the RNA-seq profiles of PPAR genes and the drug activity were downloaded from the CellMiner database (https://discover.nci.nih.gov/cellminer/). Impute package from Bioconductor (http://www.bioconductor.org/packages/release/bioc/html/impute.html) was used to preprocess the raw data. CellMiner is a web-based tool with genomic and pharmacologic information for investigators to make use of transcript and drug response data in the NCI-60 cell line sets, which was compiled by the U.S. National Cancer Institute [13]. Transcript expression levels of 22,379 genes, 360 microRNAs, and drug responses of 20,503 compounds are available in the CellMiner website [14]. To explore the correlation between the transcriptional expression of PPAR genes and compound sensitivity, we followed the methods of Dong et al. [15], and Pearson correlation analysis was performed between the two controlled by value < 0.05.

3. Results

3.1. Differential Expression Analysis and Coexpression Analysis of PPARs between Tumor and Normal Samples

The flowchart of the analysis process is summarized in Figure 1. The gene expression of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B was displayed (Figure 2(a)). Differential expression analyses with the Wilcox test were performed on 5 PPAR family genes between tumor and paratumor samples (Figure 2(b)). Those 5 PPAR genes were either down- or upregulated in most types of tumors. PPARA, PPARG, PPARGC1A, and PPARGC1B were seen with low expression in the majority of tumors while PPARD is mainly upregulated.

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Figure 2

Differential expression analysis. (a) The box plot showing the transcriptional expression levels of PPARs. (b) The heatmap showing the transcriptional level of PPARs in TCGA tumor types compared to normal tissues; the gradient colors represent the log Fold Change (logFC) value. (c–g) The box plots showing differential expression of PPARs and PPARGC1A and PPARGC1B in normal and tumor tissues (; ; ); (h) the correlation coefficients by coexpression analysis between every two genes are presented.

Specifically, compared to normal tissues, PPARA was observed with low expression in most types of tumors except pan-lung: LUAD and LUSC. It is also obvious that PPARA was the only gene in the PPAR family that was downregulated in CHOL (, Figure 2(c)). Interestingly, however, we found significant overexpression of PPARD in CHOL (, Figure 2(d)). There was a significantly differential expression of PPARG in BRCA. More than BRCA, both two lung tumors, LUAD and LUSC, expressed low PPARG (), which is opposite to PPARA as well as PPARD and different from the other 4 PPAR family genes (Figure 2(e)). Significant overexpression of PPARGC1A was observed in KICH (), and downregulation was observed in KIRC and THCA () (Figure 2(f)).

We also queried PPAR protein expressions from the Human Protein Atlas database (https://www.proteinatlas.org), and the PPAR proteins that combined to specific antibodies in both tumor and normal issues were displayed in Figure S1, which tend to follow the same expression patterns as the results of differential expression analysis.

Coexpression analysis revealed a correlation () between PPARA and PPARGC1A, suggesting a potential positive interaction between those two genes (Figure 2(h)), which was further confirmed by the protein-protein interaction (PPI) network (Figure S2). The coexpression relationship could also be observed between PPARA and PPARG (, ). By contrast, a different coexpression pattern was seen between PPARGC1A and PPAGC1B with a negative correlation (, ).

3.2. Clinical Correlation Analysis

We employed Kaplan-Meier analyses on PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B in 33 TCGA tumors (Figures 3(a)–3(f)). Based on the median gene expression values, patients were divided into high and low groups.

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Low expression of PPARA was significantly associated with poor prognosis in patients with KIRC (, Figure 3(a)), GBM (), and LGG ().

By contrast, elevated expression of PPARD was correlated with worse clinical outcomes of patients with LGG (), LIHC (), and SARC () while elevated PPARD led to better clinical outcomes in BLCA () and UVM ().

The higher expression of PPARG and PPARGC1A was associated with better prognostic outcomes in KRIC (, Figures 3(c) and 3(d)). Likewise, low expression of PPARGC1B might be a less favorable sign for clinical outcomes in patients of READ (, Figure 3(f)), which is consistent with the differentially low expression in READ compared to paratumor samples.

Cox proportional hazard regression was applied to detect the prognostic roles of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B in 33 TCGA tumors. Genes with a were considered as a prognostic factor. From the forest plot (Figure 3(g)), we found that PPARD and PPARG were of pan-cancer significance with in most cancer types.

Specifically, in STAD, we found that the expression of PPARG () and PPARGC1A () was correlated with TNM stages. The expression level of PPARG was comparatively lower in stage III and higher in stage IV. Compared to other TNM stages, the expression level of PPARGC1A was the highest in stage I, followed by stage IV, and was comparatively low in stage II and stage III (Figure 4). The difference in the expression level of PPAR family genes in different TNM stages might serve as predictors of tumor development in clinical applications.

3.3. Immune Subtype Analysis

We applied differential expression analysis with the Kruskal test on the mRNA expression of 5 PPAR genes in the six immune subtypes across 33 TCGA tumor types (Figure 5(a)).

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The expression patterns of PPARA (), PPARD (), PPARG (), PPARGC1A (), and PPARGC1B () varied in 6 immune subtypes in pan-cancers (Figure 5(a)). Obviously, PPARD ranked the first on the overall expression level in C1-C6.

In addition, different types of tumors displayed variation within immune subtypes. For the C1-C6 immune subtypes of LIHC, there were differences in the expression of PPARA (), PPARD (), and PPARGC1A () (Figure 5(b)). C6 had the highest expression of PPARA, followed by C4 and C3 while C4 has the lowest expression of PPARD. The expression level of PPARGC1A varied by immune subtypes, with C3, C4, and C6 comparatively high whereas C1 and C2 low.

In BRCA, significant differences were observed in the expression of PPAR family genes in the six immune subtypes (Figure 5(c)). In general, C4 has the lowest expression of PPAR genes. The expression of PPARA (), PPARG (), PPARGC1A (), and PPARGC1B () showed similar patterns in C1-C6, with high expression in C3 and C6 while comparatively low expression in C1, C2, and C4. PPARD, however, expressed higher in C1 and C2 compared to other immune subtypes.

For SARC, C6 had the lowest expression of PPARA () and PPARGC1A (), whereas the expression level of PPARG () was the highest among C1, C2, C3, C4, and C6 immune subtypes (Figure 5(d)).

3.4. Stemness Indices and Microtumor Environment in Pan-Cancer

Stromal scores of TCGA cancer samples were calculated by applying the ESTIMATE (Estimation of STromal and Immune cells in MAlignant Tumors using Expression data) algorithm [11]. Spearman correlation analysis was used to describe the correlation between the expression level of PPAR family genes and stromal scores in pan-cancer. As is shown in Figure 6(c), we found a positive correlation between PPARA and stromal scores in TGCT (, ). There was likewise a relationship between PPARD and LAML with a , . The expression of PPARG was positively correlated with a number of tumor types, including BRCA, DLBC, LGG, MESO, OV, PCPG, PRAD, SARC, and SKCM, suggesting that elevated expression of PPARG was associated with lower tumor purity in many types of tumors. Significant differences were found between PPARGC1A and PPARGC1B towards their relationship with tumor purity. The higher expression of PPARGC1A was correlated with high tumor purity in CHOL, GBM, KIRC, KIRP, and THCA, while with low stromal scores of BLCA, HNSC, LUSC, and TGCT, which was the opposite to the pattern of PPARGC1B.

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Figure 6

The results of correlation analysis between members of PPAR and stemness indices and microenvironment scores. (a, b) The two heatmaps showing the correlation of the expression level of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B and stemness indices (DNAss and RNAss) in 33 TCGA cancer types. DNAss: DNA methylation-based stemness score; RNAss: RNA-based stemness score. (c) The heatmap showing the correlation between stromal scores and the mRNA expression of PPARs (red points represent a positive correlation while blue points represent a negative correlation).

To analyze the correlation between PPARs and stemness features of pan-cancer, we calculated the stemness indices of TCGA tumor samples by using a one-class logistic regression (OCLR) algorithm and performed Spearman correlation analysis based on gene expression and stemness scores [12]. Two types of stemness indices were accessed, which included DNA methylation-based stemness index (DNAss) and mRNA expression-based stemness index (RNAss).

There were differences between the two stemness indices on the correlation with the PPAR expression level in TCGA tumors. For DNAss, it is obvious that there were strong correlations between TGCT and PPAR family genes, with positive correlations of PPARD (, ), PPARG (, ), and PPARGC1B (, ) and negative correlations of PPARA (, ) and PPARGC1A (, ) (Figure 6(a)).

For RNAss, strong negative correlations were observed between TGCT RNAss and PPARA (, ), between THYM RNAss and PPARD (, ), between PCPG RNAss and PPARG (, ), and between PRAD RNAss and PPARGC1A (, ) (Figure 6(b)). A positive association between the expression profiles of PPARGC1B and the RNAss of TGCT was detected (, ), suggesting that PPARGC1B might correlate with the stemness in TGCT.

In BRCA (Figure 7(a)), specifically, the expression profiles of PPARA was positively correlated with BRCA stromal scores (, ), immune scores (, ), and ESTIMATE score (, ). The expression profiles of PPARD were positively correlated with BRCA DNAss (, ), immune scores (, ), and ESTIMATE score (, ). Notably, we found negative correlations between PPARG expression with RNAss (, ) and DNAss (, ) while positive correlations with BRCA’s stromal score (, ), immune score (, ), and ESTIMATE score (, ). In addition, slight but statistically significant correlations were found between PPARGC1A and stemness indices and tumor purity. There were strong correlations, however, between PPARGC1B and stromal score (, ), immune score (, ), and ESTIMATE score (, ).

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For LIHC (Figure 7(b)), however, there were slight correlations between each PPAR family gene and stemness indices and TME except relatively strong associations between PPARA and tumor purity (stromal score: , ; immune score: , ; and ESTIMATE score: , ).

3.5. Drug Sensitivity Analysis in Pan-Cancer

To analyze the potential effects of the PPAR family on drug response, we performed Pearson correlation analysis between the transcriptional expression of PPAR family genes in NCI-60 cancer cell lines and drug activity of 263 antineoplastic drugs retrieved from the CellMiner database [16].

The scatter plots that displayed a significant correlation relationship between drug sensitivity and gene expression are presented in Figure 8 and ranked by the value, selected by . Notably, PPARGC1B was positively correlated with the sensitivity of Bafetinib (, ) and Nilotinib (, ) and the resistance of staurosporine (, ). The sensitivity of dabrafenib, a selective inhibitor of mutated forms of BRAF kinase for BRAF-mutated melanoma, thyroid cancer, and non-small-cell lung cancer, was found to be positively associated with PPARGC1A (, ) and PPARGC1B (, ). Highly expressed PPARG tumor cells were more resistant to carboplatin (, ), cisplatin (, ), arsenic trioxide (, ), and lomustine (, ) (Figure 8).

4. Discussion

In the present study, we aimed to explore the correlation of PPAR transcriptional expression with TCGA tumor features, which include TME, clinical significance, immune subtypes, stemness, and drug responses. PPAR isotypes showed distinct effects on tumor development. Using multidimensional analysis, we first performed differential expression analysis on a total of 11,057 samples (10,327 tumor samples and 730 adjacent samples) across 33 TCGA cancer types and found significant difference on the PPARs’ expression level in different tumor types. We also applied survival analysis and Cox proportional hazard regression. Statistically significant survival differences were observed between high and low PPAR-expressed patients in some types of cancers, suggesting that PPARs might become potential prognostic indicators for clinical applications.

It is also worth noting that PPARG along with PPARGC1A was found to be differentially expressed in the 4 stages of stomach adenocarcinoma, with highest PPARG in stage IV, which is consistent with the findings of Nagy et al. that PPARG may contribute to STAD carcinogenesis [17]. In this study, however, PPARG was found to have low expression in the majority of TCGA cancers. Evidence backed for PPARG’s antineoplastic actions in inducing cell cycle arrest, terminal differentiation, and anti-inflammatory effect [18]. Troglitazone (TGZ), a PPARG agonist, was reported to induce G2/M cell cycle arrest through activation of p38 mitogen-activated protein kinase in renal cell carcinoma [18, 19], and similar effects were also seen in bladder cancer cells [20]. Another agonist of PPARG, curcumin, was able to eliminate oxidative stress and chronic inflammation via downregulating the WNT/β-catenin pathway, which is observed to have aberrant activation in many cancers [21]. Sporadically, the tumor-promoting side of PPARG was observed in some cancers; it is easy to infer that the precise effects of PPARG and its agonists might depend on types of cancers and tumor environment.

Moreover, according to the C1-C6 immune subtypes previously identified by investigators [10], we classified tumor samples by representative immune signatures and examined the RNA-seq level of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B from C1 to C6, which were all seen to have differential expressions. These immune features along with extracellular matrix, tumor vasculature, and tumor cells make up the concept of the tumor microenvironment (TME), the heterogeneity of which highly influences therapeutic response and clinical prognosis [22]. Thus, we further accessed the fractions of stromal cells and immune cells in tumor samples of 33 TCGA cancer types by calculating stromal scores, immune scores, and ESTIMATE scores. Those TME characteristics were correlated with the expression level of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B. Unexpectedly, correlations did exist in some types of cancers. In breast invasive carcinoma, particularly, PPARG and PPARGC1B were negatively correlated with tumor purity.

Stemness has been proposed to describe the stem cell-like characteristics of the tumor: self-renewal and dedifferentiation [23]. The acquisition of stem cell-like properties has been reported to be found in many tumor progression [24]. Here, we utilized an OCLR approach to calculate the RNAss score and DNAss score of tumor samples and then correlated it with transcriptional signatures of PPARs. We found an association between PPARs and stemness within tumors, suggesting that PPARs may play a role in stemness maintenance.

This study also found that the transcriptional expression level of PPARs, PPARG1A, and PPARG1B was associated with drug responses. Notably, high expression of PPAGC1B was even more sensitive to Bafetinib and Nilotinib across cancer treatments, which is of clinical significance for selection of antitumor therapies.

The three isotypes of peroxisome proliferator-activated receptors differ in both physiological functions and roles in carcinogenesis. PPARα, encoded by PPARA, mainly enriches in the liver, kidney, and heart, regulating fatty acid metabolism and mitochondrial biosynthesis [25]. In addition to its endogenous ligands (fatty acids), PPARα responds to the PPARα agonists (synthetic fibrates), such as fenofibrate and gemfibrozil, which have been working well in the treatment for hypolipidemic diseases [26]. Moreover, PPARα agonists have been reported to show antitumor effects in colon carcinogenesis. However, it is still controversial whether the roles of PPARα is cancer-repressing or cancer-promoting [25]. Some studies suggested that long-term activation of PPARα induced hepatocellular carcinoma in mice and was essential for the development of hepatic steatosis [27]. The roles of PPARα in carcinogenesis require further elucidation. PPARG, encoding PPARγ, functions as a key regulator of glucose homeostasis and adipocyte differentiation [28]. Downregulation of PPARγ is associated with decreased terminal differentiation and cell cycle arrest, which induces cell proliferation and leads to tumorigenesis [7, 29]. The potential mechanism was proposed by Drori et al. that the PPARγ-induced differentiation may be mediated by a putative PPARγ coactivator, HIC5, suggesting the importance of coactivators in PPARγ signaling [30]. Peroxisome proliferator-activated receptor coactivators 1 alpha and beta (PPAGC1A and PPARGC1B, respectively) cooperate with PPARPγ, allowing the subsequent interaction between PPARγ and other transcription factors [31, 32]. Pharmacological activators of PPARδ also show controversial effects on the hallmarks of caner, which may depend on the type of PPARδ ligands and target tissues [33, 34].

Although this study is the first one to multidimensionally analyze peroxisome proliferator-activated receptors (PPARs) in pan-cancer, it still possessed some limitations that warrant consideration. Firstly, all the samples involved in this study were from America, and thus, we were not quite sure about the applicability of the prediction model in Europe and Asia. Second, the results of this study have not been verified by other independent databases, and thus, our future work is validating it by our own data and other public database. Third, the potential mechanism in this study is based on bioinformatics analysis and has not been verified by molecular and animal experiments. The analysis of this study focuses on the correlation between the PPAR family and multiple omics data. However, the biostatistical correlation could not elucidate the direct interaction and direct regulation mechanism, which should be the main limitation of this study. Thus, we plan to verify these potential mechanisms via molecular experiments. Further investigations are required to figure out the potentials of PPARs and their coactivators as drug targets for cancer, which makes our study even more important in the contribution to the expression signature analysis of PPARA, PPARD, PPARG, PPARGC1A, and PPARGC1B.

5. Conclusion

We performed multidimensional analyses on PPARA, PPARG, PPARD, PPARGC1A, and PPARGC1B, including differential expression analysis in pan-cancer, immune subtype analysis, clinical analysis, tumor purity analysis, stemness correlation analysis, and drug responses. PPARs and their coactivators expressed differently in different types of cancers, in different immune subtypes. This analysis reveals various expression patterns of the PPAR family at a level of pan-cancer and provides new clues for the therapeutic strategies of cancer.

Data Availability

The datasets generated and/or analyzed during the current study are available in Supplementary Materials and TCGA program (https://portal.gdc.cancer.gov).

Ethical Approval

The study was approved by the Ethics Committee of the First Affiliated Hospital of Zhengzhou University.

Disclosure

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Conflicts of Interest

The authors declare that there is no conflict of interests.

Authors’ Contributions

Runzhi Huang, Jiaqi Zhang, Peng Hu, Penghui Yan, Huabin Yin, Suna Zhai, Xiaolong Zhu, Jiaxin Zhang, Mingxiao Li, Ling Huang, Man Li, Zehui Sun, Tong Meng, Daoke Yang, and Zongqiang Huang worked on conception/design, collection and/or assembly of data, data analysis and interpretation, manuscript writing, and final approval of manuscript.

Acknowledgments

We thank The Cancer Genome Atlas (TCGA) team for the use of their data. This study was supported in part by the National Natural Science Foundation of China (Grant Nos. 81702659 and 81772856); National Natural Science Foundation of China, joint fund cultivation project (Grant No. U1504822); Youth Fund of Shanghai Municipal Health Planning Commission (No.2017YQ054); Henan Medical Science and Technology research project (No. 201602031); Henan Medical Science and technology research plan, joint project of the Ministry and the province (No. SB201901037); and Henan Provincial Department of science and technology, social development project (No. 142102310055).

Supplementary Materials

Figure S1: PPAR protein expression in cancer (breast cancer, colon adenocarcinoma, and prostate cancer) and normal tissues from the Human Protein Atlas database. Figure S2: the protein-protein interaction (PPI) network constructed among PPARA, PPARD, PPARG, PPARGC1A, PPARGC1B, and their top related genes. (Supplementary Materials)

References

V. Dubois, J. Eeckhoute, P. Lefebvre, and B. Staels, “Distinct but complementary contributions of PPAR isotypes to energy homeostasis,” The Journal of Clinical Investigation, vol. 127, no. 4, pp. 1202–1214, 2017.
View at: Publisher Site | Google Scholar
J. Youssef and M. Badr, “Peroxisome proliferator-activated receptors and cancer: challenges and opportunities,” British Journal of Pharmacology, vol. 164, no. 1, pp. 68–82, 2011.
View at: Publisher Site | Google Scholar
J. D. Brown and J. Plutzky, “Peroxisome proliferator-activated receptors as transcriptional nodal points and therapeutic targets,” Circulation, vol. 115, no. 4, pp. 518–533, 2007.
View at: Publisher Site | Google Scholar
C. Pirat, A. Farce, N. Lebègue et al., “Targeting peroxisome proliferator-activated receptors (PPARs): development of modulators,” Journal of Medicinal Chemistry, vol. 55, no. 9, pp. 4027–4061, 2012.
View at: Publisher Site | Google Scholar
E. Sahin, S. Colla, M. Liesa et al., “Telomere dysfunction induces metabolic and mitochondrial compromise,” Nature, vol. 470, no. 7334, pp. 359–365, 2011.
View at: Publisher Site | Google Scholar
B. Gross, M. Pawlak, P. Lefebvre, and B. Staels, “PPARs in obesity-induced T2DM, dyslipidaemia and NAFLD,” Nature Reviews Endocrinology, vol. 13, no. 1, pp. 36–49, 2017.
View at: Publisher Site | Google Scholar
J. M. Peters, Y. M. Shah, and F. J. Gonzalez, “The role of peroxisome proliferator-activated receptors in carcinogenesis and chemoprevention,” Nature Reviews Cancer, vol. 12, no. 3, pp. 181–195, 2012.
View at: Publisher Site | Google Scholar
A. Z. Mirza, I. I. Althagafi, and H. Shamshad, “Role of PPAR receptor in different diseases and their ligands: physiological importance and clinical implications,” European Journal of Medicinal Chemistry, vol. 166, pp. 502–513, 2019.
View at: Publisher Site | Google Scholar
D. Szklarczyk, A. L. Gable, D. Lyon et al., “STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets,” Nucleic Acids Research, vol. 47, no. D1, pp. D607–D613, 2019.
View at: Publisher Site | Google Scholar
V. Thorsson, D. L. Gibbs, S. D. Brown et al., “The immune landscape of cancer,” Immunity, vol. 48, no. 4, pp. 812–830.e14, 2018, e14.
View at: Publisher Site | Google Scholar
K. Yoshihara, M. Shahmoradgoli, E. Martínez et al., “Inferring tumour purity and stromal and immune cell admixture from expression data,” Nature Communications, vol. 4, no. 1, 2013.
View at: Publisher Site | Google Scholar
T. M. Malta, A. Sokolov, A. J. Gentles et al., “Machine learning identifies stemness features associated with oncogenic dedifferentiation,” Cell, vol. 173, no. 2, pp. 338–354.e15, 2018, e15.
View at: Publisher Site | Google Scholar
W. C. Reinhold, M. Sunshine, H. Liu et al., “CellMiner: a web-based suite of genomic and pharmacologic tools to explore transcript and drug patterns in the NCI-60 cell line set,” Cancer Research, vol. 72, no. 14, pp. 3499–3511, 2012.
View at: Publisher Site | Google Scholar
U. T. Shankavaram, S. Varma, D. Kane et al., “CellMiner: a relational database and query tool for the NCI-60 cancer cell lines,” BMC Genomics, vol. 10, no. 1, p. 277, 2009.
View at: Publisher Site | Google Scholar
X. Dong, D. Huang, X. Yi et al., “Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes,” Communications Biology, vol. 3, no. 1, p. 6, 2020.
View at: Publisher Site | Google Scholar
A. Puszkiel, G. Noé, A. Bellesoeur et al., “Clinical pharmacokinetics and pharmacodynamics of dabrafenib,” Clinical Pharmacokinetics, vol. 58, no. 4, pp. 451–467, 2019.
View at: Publisher Site | Google Scholar
T. A. Nagy, L. E. Wroblewski, D. Wang et al., “β-Catenin and p120 mediate PPARδ-dependent proliferation induced by _Helicobacter pylori_ in human and rodent epithelia,” Gastroenterology, vol. 141, no. 2, pp. 553–564, 2011.
View at: Publisher Site | Google Scholar
B. Bandera Merchan, F. J. Tinahones, and M. Macias-Gonzalez, “Commonalities in the association between PPARG and vitamin D related with obesity and carcinogenesis,” PPAR Research, vol. 2016, Article ID 2308249, 15 pages, 2016.
View at: Publisher Site | Google Scholar
M. Fujita, T. Yagami, M. Fujio et al., “Cytotoxicity of troglitazone through PPARγ-independent pathway and p38 MAPK pathway in renal cell carcinoma,” Cancer Letters, vol. 312, no. 2, pp. 219–227, 2011.
View at: Publisher Site | Google Scholar
M. L. Plissonnier, S. Fauconnet, H. Bittard, and I. Lascombe, “Insights on distinct pathways of thiazolidinediones (PPARγ ligand)-promoted apoptosis in TRAIL-sensitive or -resistant malignant urothelial cells,” International Journal of Cancer, vol. 127, no. 8, pp. 1769–1784, 2010.
View at: Publisher Site | Google Scholar
A. Vallee, Y. Lecarpentier, and J. N. Vallee, “Curcumin: a therapeutic strategy in cancers by inhibiting the canonical WNT/β-catenin pathway,” Journal of Experimental & Clinical Cancer Research, vol. 38, no. 1, p. 323, 2019.
View at: Publisher Site | Google Scholar
M. R. Junttila and F. J. de Sauvage, “Influence of tumour micro-environment heterogeneity on therapeutic response,” Nature, vol. 501, no. 7467, pp. 346–354, 2013.
View at: Publisher Site | Google Scholar
D. Friedmann-Morvinski and I. M. Verma, “Dedifferentiation and reprogramming: origins of cancer stem cells,” EMBO Reports, vol. 15, no. 3, pp. 244–253, 2014.
View at: Publisher Site | Google Scholar
A. Miranda, P. T. Hamilton, A. W. Zhang et al., “Cancer stemness, intratumoral heterogeneity, and immune response across cancers,” Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 18, pp. 9020–9029, 2019.
View at: Publisher Site | Google Scholar
Y. Luo, C. Xie, C. N. Brocker et al., “Intestinal PPARα protects against colon carcinogenesis via regulation of methyltransferases DNMT1 and PRMT6,” Gastroenterology, vol. 157, no. 3, pp. 744–759.e4, 2019, e4.
View at: Publisher Site | Google Scholar
I. Takada and M. Makishima, “Peroxisome proliferator-activated receptor agonists and antagonists: a patent review (2014-present),” Expert Opinion on Therapeutic Patents, vol. 30, no. 1, pp. 1–13, 2020.
View at: Publisher Site | Google Scholar
N. Tanaka, K. Moriya, K. Kiyosawa, K. Koike, F. J. Gonzalez, and T. Aoyama, “PPARalpha activation is essential for HCV core protein-induced hepatic steatosis and hepatocellular carcinoma in mice,” The Journal of Clinical Investigation, vol. 118, no. 2, pp. 683–694, 2008.
View at: Publisher Site | Google Scholar
G. T. Robbins and D. Nie, “PPAR gamma, bioactive lipids, and cancer progression,” Frontiers in Bioscience, vol. 17, no. 1, pp. 1816–1834, 2012.
View at: Publisher Site | Google Scholar
H. R. Dhaini and Z. Daher, “Genetic polymorphisms of PPAR genes and human cancers: evidence for gene-environment interactions,” Journal of Environmental Science and Health. Part C, Environmental Carcinogenesis & Ecotoxicology Reviews, vol. 37, no. 3, pp. 146–179, 2019.
View at: Publisher Site | Google Scholar
S. Drori, “Hic-5 regulates an epithelial program mediated by PPAR,” Genes & Development, vol. 19, no. 3, pp. 362–375, 2005.
View at: Publisher Site | Google Scholar
M. Wirtenberger, S. Tchatchou, K. Hemminki et al., “Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer,” Carcinogenesis, vol. 27, no. 11, pp. 2201–2208, 2006.
View at: Publisher Site | Google Scholar
M. Petr, P. Stastny, A. Zajac, J. Tufano, and A. Maciejewska-Skrendo, “The role of peroxisome proliferator-activated receptors and their transcriptional coactivators gene variations in human trainability: a systematic review,” International Journal of Molecular Sciences, vol. 19, no. 5, p. 1472, 2018.
View at: Publisher Site | Google Scholar
K. D. Wagner and N. Wagner, “Peroxisome proliferator-activated receptor beta/delta (PPARβ/δ) acts as regulator of metabolism linked to multiple cellular functions,” Pharmacology & Therapeutics, vol. 125, no. 3, pp. 423–435, 2010.
View at: Publisher Site | Google Scholar
N. Wagner and K. D. Wagner, “PPAR beta/delta and the hallmarks of cancer,” Cell, vol. 9, no. 5, p. 1133, 2020.
View at: Publisher Site | Google Scholar

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Copyright © 2020 Runzhi Huang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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