Abstract

Prostate cancer is among the top mortality factors in male around the world. Long non-coding RNAs (lncRNAs) have been shown to play crucial roles in tumor biology and immunology. However, lncRNA-immune interactions have not yet examined in prostate cancer. Here, we performed integrated analysis to characterize lncRNA-immune interactions in prostate cancer through multidimensional aspects, including immune-related hallmarks, tumor immunogenomic signatures, immune-related biological processes, immune cells, and immune checkpoints. We dissected the dysregulation of lncRNAs and their clinical relevance in prostate cancer, such as RP11-627G23.1 and RP11-465N4.5. Immune-related hallmarks took up the major parts among top significant lncRNA-hallmark interactions. Our analysis revealed that TGF-β signaling pathway was the most frequent to associate with lncRNAs, which is a signature of immune response in cancer. In addition, immune response and its regulation were the most closely connected immunological processes with lncRNA, implying the regulatory roles of lncRNAs on immune response in prostate cancer. We found that memory resting CD4+ T cells were the most lncRNA-correlated immune cell. LINC00861 was found to be potentially intervening targets of immunotherapy for prostate cancer patients, which was significantly associated with PD-1 and CTLA4. Collectively, we offered a handy resource to investigate regulatory roles of lncRNAs on tumor immunology and the development of clinical utility of lncRNAs in prostate cancer.

Highlights

  • Prostate cancer is the most common malignancy in male, especially in Western World (Ferlay et al, 2015; Ku et al, 2019; Siegel et al, 2020)

  • To comprehensively characterize the long non-coding RNA (lncRNA)-immune interactions in prostate cancer, our study explored the relations between lncRNAs and biological hallmarks, tumor immunogenomic signatures, immune-related biological processes, infiltrated immune cells, and immune checkpoints

  • We identified prostate cancer-specific dysregulated lncRNAs and prognostic lncRNAs, such as RP11-627G23.1 and RP11465N4.5

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Summary

Introduction

Prostate cancer is the most common malignancy in male, especially in Western World (Ferlay et al, 2015; Ku et al, 2019; Siegel et al, 2020). Studies regarding molecular alterations of prostate cancer offered mounts of potential diagnostic and therapeutic targets, with non-coding RNAs playing important roles (Ku et al, 2019). Transcriptome diversity and their connections with critical biological processes have been investigated in multiple cancer types, among which non-coding RNAs took a large part. LncRNAs have been shown to play important roles in human cancers (Iyer et al, 2015; Niknafs et al, 2016; Li S. et al, 2018; Li Z. et al, 2018), including prostate cancer (Hua et al, 2018, 2019). The landscape of aberrant lncRNAs and their interactions with immune features in prostate cancer have not been characterized

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