Influence of migrasome-associated long noncoding RNAs on the immune microenvironment and prognosis in lung adenocarcinoma

  • 0Jilin Cancer Hospital, 1066 Jinhudalu, Gaoxin District, Changchun, 130012, Jilin, China.

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Summary

This summary is machine-generated.

Migrasome-related long noncoding RNAs (lncRNAs) can predict lung adenocarcinoma (LUAD) patient outcomes and immunotherapy response. A novel risk score model identifies patients who may benefit from immune checkpoint inhibitors.

Area Of Science

  • Oncology
  • Molecular Biology
  • Bioinformatics

Background

  • Lung adenocarcinoma (LUAD) is a major cause of cancer mortality.
  • Identifying reliable prognostic biomarkers is crucial for LUAD patient management.
  • The role of migrasome-related long noncoding RNAs (lncRNAs) in LUAD prognosis remains largely unexplored.

Purpose Of The Study

  • To investigate the prognostic significance of migrasome-related lncRNAs in LUAD.
  • To develop and validate a risk score model based on these lncRNAs for predicting patient outcomes.
  • To explore the association between migrasome-related lncRNAs, tumor immune microenvironment, and immunotherapy response in LUAD.

Main Methods

  • Transcriptomic data analysis from The Cancer Genome Atlas (TCGA) database.
  • Correlation analysis to identify key migrasome-related lncRNAs associated with patient survival.
  • Construction and validation of a prognostic risk score model using Cox regression and an independent dataset.
  • Tumor Immune Dysfunction and Exclusion (TIDE) and functional enrichment analyses to assess immune features and pathways.

Main Results

  • A risk score model comprising 17 migrasome-related lncRNAs was developed and validated.
  • High-risk patients demonstrated significantly worse overall and progression-free survival.
  • The risk score correlated with altered immune features, suggesting immune evasion and potential immunotherapy responsiveness.
  • TIDE analysis indicated that higher-risk individuals might benefit more from immune checkpoint inhibitors.

Conclusions

  • Migrasome-related lncRNAs serve as robust prognostic biomarkers for LUAD.
  • The developed risk score model effectively predicts patient prognosis and informs immunotherapy decisions.
  • These lncRNAs offer potential therapeutic targets and highlight the interplay between migrasomes, lncRNAs, and tumor immunity in LUAD.

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