Propionate metabolism-related genes demonstrate the potential to serve as prognostic and immunotherapeutic markers in osteosarcoma

  • 0Department of Orthopedics, The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230601, P.R. China.

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Summary

This summary is machine-generated.

This study identifies propionate metabolism genes, ABAT and ALDH7A1, as novel prognostic indicators for osteosarcoma (OS). These genes predict patient outcomes and immune response, offering potential therapeutic targets for OS treatment.

Area Of Science

  • Oncology
  • Metabolic Research
  • Bioinformatics

Background

  • Osteosarcoma (OS) metabolic processes are crucial for developing diagnostics and therapeutics.
  • Propionate metabolism plays a significant role in certain cancers, suggesting its relevance in OS.

Purpose Of The Study

  • To identify novel prognostic indicators for OS using gene expression and clinical data.
  • To explore the role of propionate metabolism in OS and its association with patient prognosis and immune response.

Main Methods

  • Analysis of public datasets to identify differentially expressed genes (DEGs) and propionate metabolism-associated genes.
  • Construction of a risk model using LASSO-Cox regression, followed by immune cell infiltration and immunotherapy response assessment.
  • Development of a prognostic nomogram and validation through cell assays for key identified genes.

Main Results

  • Identified 18 DEGs related to propionate metabolism in OS.
  • Developed a risk model based on two prognostic genes: 4-aminobutyrate aminotransferase (ABAT) and aldehyde dehydrogenase 7 family member A1 (ALDH7A1).
  • Demonstrated significant differences in immune infiltration between high- and low-risk groups, impacting immunotherapy response. Knockdown of ABAT promoted OS cell growth and invasion.

Conclusions

  • Propionate metabolism is relevant in OS, with ABAT and ALDH7A1 serving as novel gene signatures for clinical outcome prediction.
  • The identified gene signature can distinguish OS patients with different clinical outcomes and tumor microenvironments.
  • ABAT and ALDH7A1 show potential as therapeutic targets for osteosarcoma.

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