# A prognostic model correlated with fatty acid metabolism in Ewing’s sarcoma based on bioinformatics analysis

**Authors:** Xianwei Chen, Yuqi Yang, Dongqi Li, En Ye, Bingjian He, Mingshu Yu, Jiankai Luo, Jing Zhang

PMC · DOI: 10.1515/med-2025-1238 · 2025-08-07

## TL;DR

This study develops a prognostic model for Ewing’s sarcoma based on fatty acid metabolism genes, identifying PPT1 and ACOT7 as potential predictors of patient survival.

## Contribution

The novel contribution is the construction of a fatty acid metabolism-based prognostic model for Ewing’s sarcoma using bioinformatics analysis.

## Key findings

- A risk model with seven fatty acid metabolism-related genes showed good predictive accuracy with AUC values ≥0.7 at 3 and 5 years.
- High- and low-risk groups differed significantly in fatty acid metabolism pathway enrichment and immune cell infiltration.
- PPT1 and ACOT7 protein expression was associated with progression-free survival in EWS patients.

## Abstract

Ewing’s sarcoma (EWS) is a highly aggressive malignant tumor that originates from bone or soft tissue. To date, there is no established prognostic model for EWS tumor. This study aims to identify prognostic genes and develop a predictive model associated with fatty acid metabolism in EWS using bioinformatics analysis.

We analyzed the GSE17679 dataset and identified 25 differentially expressed genes related to fatty acid metabolism in EWS. A risk model composed of ACADM, ADH5, ACSL1, ELOVL4, ECI1, PPT1, and ACOT7 gene signatures was constructed. The AUC values at 3 and 5 years were both ≥0.7, indicating good predictive accuracy. GSVA analysis revealed significant differences in fatty acid metabolism pathway enrichment between high- and low-risk groups. Differential genes were primarily enriched in pathways such as fatty acid oxidation, lipid oxidation, lipid modification, and fatty acid degradation. Immune infiltration analysis showed significant differences in memory B cells, activated NK cells, and neutrophils between the two groups. Additionally, significant differences were observed in the expression of immune checkpoints such as HAVCR2 and LDHB. Immunohistochemistry and survival analysis further demonstrated that the expression of PPT1 and ACOT7 proteins was associated with the progression-free survival of EWS patients.

We successfully constructed a prognostic model for EWS related to fatty acid metabolism genes. PPT1 and ACOT7 may serve as promising predictors for EWS prognosis.

## Linked entities

- **Genes:** ACADM (acyl-CoA dehydrogenase medium chain) [NCBI Gene 34], ADH5 (alcohol dehydrogenase 5 (class III), chi polypeptide) [NCBI Gene 128], ACSL1 (acyl-CoA synthetase long chain family member 1) [NCBI Gene 2180], ELOVL4 (ELOVL fatty acid elongase 4) [NCBI Gene 6785], ECI1 (enoyl-CoA delta isomerase 1) [NCBI Gene 1632], PPT1 (palmitoyl-protein thioesterase 1) [NCBI Gene 5538], ACOT7 (acyl-CoA thioesterase 7) [NCBI Gene 11332], HAVCR2 (hepatitis A virus cellular receptor 2) [NCBI Gene 84868], LDHB (lactate dehydrogenase B) [NCBI Gene 3945]
- **Proteins:** PPT1 (palmitoyl-protein thioesterase 1), ACOT7 (acyl-CoA thioesterase 7)
- **Diseases:** Ewing’s sarcoma (MONDO:0012817)

## Full-text entities

- **Genes:** ACADM (acyl-CoA dehydrogenase medium chain) [NCBI Gene 34] {aka ACAD1, MCAD, MCADH}, ACSL1 (acyl-CoA synthetase long chain family member 1) [NCBI Gene 2180] {aka ACS1, FACL1, FACL2, LACS, LACS1, LACS2}, HAVCR2 (hepatitis A virus cellular receptor 2) [NCBI Gene 84868] {aka CD366, HAVcr-2, KIM-3, SPTCL, TIM3, TIMD-3}, ACOT7 (acyl-CoA thioesterase 7) [NCBI Gene 11332] {aka ACH1, ACT, BACH, CTE-II, LACH, LACH1}, ECI1 (enoyl-CoA delta isomerase 1) [NCBI Gene 1632] {aka DCI}, PPT1 (palmitoyl-protein thioesterase 1) [NCBI Gene 5538] {aka CLN1, INCL, PPT}, LDHB (lactate dehydrogenase B) [NCBI Gene 3945] {aka HEL-S-281, LDH-B, LDH-H, LDHBD, TRG-5}, ELOVL4 (ELOVL fatty acid elongase 4) [NCBI Gene 6785] {aka ADMD, CT118, ISQMR, SCA34, STGD2, STGD3}, ADH5 (alcohol dehydrogenase 5 (class III), chi polypeptide) [NCBI Gene 128] {aka ADH-3, ADHX, AMEDS, BMFS7, FALDH, FDH}
- **Diseases:** EWS (MESH:D012512), malignant tumor (MESH:D009369)
- **Chemicals:** fatty acid (MESH:D005227), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12355353/full.md

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Source: https://tomesphere.com/paper/PMC12355353