Abstract

BackgroundEmerging evidences have indicated that the aberrant liquid–liquid phase separation (LLPS) leads to the dysfunction of biomolecular condensates, thereby contributing to the tumorigenesis and progression. Nevertheless, it remains unclear whether or how the LLPS of specific molecules affects the prognosis and tumor immune microenvironment (TIME) of patients with lower-grade glioma (LGG).MethodsWe integrated the transcriptome information of 3585 LLPS-related genes to comprehensively evaluate the LLPS patterns of 423 patients with LGG in The Cancer Genome Atlas (TCGA) cohort. Then, we systematically demonstrated the differences among four LLPS subtypes based on multi-omics analyses. In addition, we constructed the LLPS-related prognostic risk score (LPRS) for individualized integrative assessment.ResultsBased on the expression profiles of 85 scaffolds, 355 regulators, and 3145 clients in LGG, we identified four LLPS subtypes, namely LS1, LS2, LS3 and LS4.We confirmed that there were significant differences in prognosis, clinicopathological features, cancer hallmarks, genomic alterations, TIME patterns and immunotherapeutic responses among four LLPS subtypes. In addition, a prognostic signature called LPRS was constructed for individualized integrative assessment. LPRS exhibited a robust predictive capacity for prognosis of LGG patients in multiple cohorts. Moreover, LPRS was found to be correlated with clinicopathological features, cancer hallmarks, genomic alterations and TIME patterns of LGG patients. The predictive power of LPRS in response to immune checkpoint inhibitor (ICI) therapy was also prominent.ConclusionsThis study provided a novel classification of LGG patients based on LLPS. The constructed LPRS might facilitate individualized prognosis prediction and better immunotherapy options for LGG patients.

Highlights

  • The understanding of the pathogenesis of human tumors is incomplete, which dramatically limits the development of effective treatment strategies

  • A prognostic signature called LLPS-related prognostic risk score (LPRS) was constructed for individualized integrative assessment

  • LPRS was found to be correlated with clinicopathological features, cancer hallmarks, genomic alterations and tumor immune microenvironment (TIME) patterns of lower-grade glioma (LGG) patients

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Summary

Introduction

The understanding of the pathogenesis of human tumors is incomplete, which dramatically limits the development of effective treatment strategies. Emerging evidences indicate that a large proportion of tumor malignant phenotypes originate from the intrinsically disordered domains (IDRs) of protein [1–. The function of proteins with IDRs has been proved to be regulated by the liquid–liquid phase separation (LLPS) process [4,5,6]. Emerging evidences have indicated that the aberrant liquid–liquid phase separation (LLPS) leads to the dysfunction of biomolecular condensates, thereby contributing to the tumorigenesis and progression. It remains unclear whether or how the LLPS of specific molecules affects the prognosis and tumor immune microenvironment (TIME) of patients with lower-grade glioma (LGG)

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