Frontiers in Medicine (Aug 2023)

Development and validation of a novel necroptosis-related gene signature for predicting prognosis and therapeutic response in Ewing sarcoma

  • Runhan Zhao,
  • Runhan Zhao,
  • Yu Jiang,
  • Jun Zhang,
  • Jun Zhang,
  • Yanran Huang,
  • Yanran Huang,
  • Chuang Xiong,
  • Chuang Xiong,
  • Zenghui Zhao,
  • Zenghui Zhao,
  • Tianji Huang,
  • Tianji Huang,
  • Wei Liu,
  • Wei Liu,
  • Nian Zhou,
  • Nian Zhou,
  • Zefang Li,
  • Zefang Li,
  • Xiaoji Luo,
  • Xiaoji Luo,
  • Yongli Tang

DOI
https://doi.org/10.3389/fmed.2023.1239487
Journal volume & issue
Vol. 10

Abstract

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Ewing sarcoma (ES) is the second most common malignant bone tumor in children and has a poor prognosis due to early metastasis and easy recurrence. Necroptosis is a newly discovered cell death method, and its critical role in tumor immunity and therapy has attracted widespread attention. Thus, the emergence of necroptosis may provide bright prospects for the treatment of ES and deserves our further study. Here, based on the random forest algorithm, we identified 6 key necroptosis-related genes (NRGs) and used them to construct an NRG signature with excellent predictive performance. Subsequent analysis showed that NRGs were closely associated with ES tumor immunity, and the signature was also good at predicting immunotherapy and chemotherapy response. Next, a comprehensive analysis of key genes showed that RIPK1, JAK1, and CHMP7 were potential therapeutic targets. The Cancer Dependency Map (DepMap) results showed that CHMP7 is associated with ES cell growth, and the Gene Set Cancer Analysis (GSCALite) results revealed that the JAK1 mutation frequency was the highest. The expression of 3 genes was all negatively correlated with methylation and positively with copy number variation (CNV). Finally, an accurate nomogram was constructed with this signature and clinical traits. In short, this study constructed an accurate prognostic signature and identified 3 novel therapeutic targets against ES.

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