Abstract

BackgroundThe toll-like receptor 4 (TLR4) agonist, Bacille Calmette-Guérin, has exhibited gratifying effects in treating bladder cancer. The study aims to explore the expression pattern, prognostic value, and potential mechanism of TLR4 in bladder cancer.MethodsThe transcriptome file from the GSE13507 dataset in the Gene Expression Omnibus database and the promoter methylation file from the bladder cancer dataset in The Cancer Genome Atlas database were downloaded for analysis. The prognostic value of the TLRs was assessed by univariate Cox regression. Immunohistochemistry was applied to verify the expression of TLR4 in bladder cancer. The drug response is estimated through the R package “pRRophetic.” The CIBERSORT algorithm was carried out to estimate the infiltrating immune cells of samples. Gene Set Enrichment Analysis (GSEA) was performed to identify the pathways involved under varied TLR4 expression levels.ResultsTLR4 is decreased in tumor tissues compared with surrounding tumor tissues or normal tissue, which is also positively correlated to the overall survival rate (hazard ratio [HR] = 0.38) and cancer-specific survival rate (HR = 0.15) of patients with bladder cancer. Low expression of TLR4 is observed in tumors with malignant performance (high pathological grade, higher tumor stage, and progression). Patients with low TLR4 levels are more sensitive to gemcitabine rather than cisplatin. The promoter methylation level of TLR4 is positively associated with TLR4 expression (P < 0.001). The cg14629571 methylation site largely contributes to the overall methylation level. The CIBERSORT analysis shows that high TLR4 expression is associated with lower levels of plasma cells, M0 macrophages, and M1 macrophages. The GSEA results indicate that the TGF-β pathway and apoptosis are activated in high TLR4 bladder cancer, while G2M checkpoint and E2F targets pathways are enriched in low TLR4 bladder cancer.ConclusionThis research discusses the abnormal expression and prognostic value of TLR4 in bladder cancer. The TLR4 expression can effectively predict oncological outcomes and drug sensitivity of bladder cancer patients. TLR4 is also associated with infiltrating immune cell variation and cancer pathway dysregulation. The results provide a novel prognostic marker and potential drug targets for bladder cancer.

Highlights

  • Toll-like receptors (TLRs), including TLR1 to TLR10, belong to a class of highly conserved molecules

  • A typical example is the utilization of Bacille Calmette-Guérin (BCG), a TLR2, toll-like receptor 4 (TLR4), and TLR9 triagonist, in preventing recurrence of non-muscle invasive bladder cancer (NMIBC; Babjuk et al, 2020)

  • As for TLR4, the expression is reduced in tumor tissue compared to normal tissue (P = 0.077) and surrounding tumor tissue (P = 0.0085; Figure 1B)

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Summary

Introduction

Toll-like receptors (TLRs), including TLR1 to TLR10, belong to a class of highly conserved molecules. TLRs are mainly expressed in immune cells to recognize pathogen-associated molecular patterns or damage-associated molecular patterns (Kawasaki and Kawai, 2014). Recent studies reveal the antitumor effects of TLRs (Ayala-Cuellar et al, 2019). Certain TLR agonists have been applied in clinical practice. A typical example is the utilization of Bacille Calmette-Guérin (BCG), a TLR2, TLR4, and TLR9 triagonist, in preventing recurrence of non-muscle invasive bladder cancer (NMIBC; Babjuk et al, 2020). The toll-like receptor 4 (TLR4) agonist, Bacille Calmette-Guérin, has exhibited gratifying effects in treating bladder cancer. The study aims to explore the expression pattern, prognostic value, and potential mechanism of TLR4 in bladder cancer

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