Assessing the mechanism of osteosarcoma induced by long-term PET exposure: prediction from combined network toxicology, machine learning and molecular docking

This study reveals that PET may play a critical role in OS development by regulating hub genes and signaling pathways. Molecular docking analysis demonstrates that PET can tightly bind to specific target proteins, suggesting a potential molecular mechanism underlying OS progression. These findings provide a scientific basis for further evaluating PET-related health risks and offer theoretical support for the development of future prevention and treatment strategies.

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Publication Details

Journal
Journal of bone oncology
Published
2025-09-23
DOI
https://doi.org/10.1016/j.jbo.2025.100714
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
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article

Assessing the mechanism of osteosarcoma induced by long-term PET exposure: prediction from combined network toxicology, machine learning and molecular docking

Rüdiger von Eisenhart‐Rothe, Anna Curto, Yu Qiao, Fahu Yuan et al.
Journal of bone oncology
Computational Drug Discovery Methods
article

Assessing the mechanism of osteosarcoma induced by long-term PET exposure: prediction from combined network toxicology, machine learning and molecular docking

Rüdiger von Eisenhart‐Rothe, Anna Curto, Yu Qiao, Fahu Yuan, Florian Hinterwimmer
article en

Abstract

This study reveals that PET may play a critical role in OS development by regulating hub genes and signaling pathways. Molecular docking analysis demonstrates that PET can tightly bind to specific target proteins, suggesting a potential molecular mechanism underlying OS progression. These findings provide a scientific basis for further evaluating PET-related health risks and offer theoretical support for the development of future prevention and treatment strategies.

Journal of bone oncologyVol. 55
Jianghan University (CN), Technical University of Munich (DE)
Openalex Percentile: Top 70%
Computational Drug Discovery Methods
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