# Global research landscape and multisystem health mechanisms of luteolin: a comprehensive bibliometric and network pharmacology study

**Authors:** Huina Guo, Xiyan Tian, Haiyan Wang, Kexin Wang, Qi Han, Yujia Guo, Xiaoya Guan, Zhongxun Li, Xin Wen, Bohui Wu, Liting Zhao, Ying Wang, Hongliang Liu, Chunming Zhang

PMC · DOI: 10.3389/fnut.2026.1758832 · Frontiers in Nutrition · 2026-01-28

## TL;DR

This study maps luteolin research trends and mechanisms from 2000 to 2025, revealing its potential for health benefits and disease prevention through multiple biological pathways.

## Contribution

The study introduces a comprehensive bibliometric and network pharmacology analysis of luteolin's mechanisms and research trends.

## Key findings

- Luteolin research has shown sustained growth, especially after 2021, with a shift in focus to metabolic health and immune regulation.
- Network pharmacology identified 239 potential targets, including TP53 and TNF, enriched in key pathways like p53 and PI3K–Akt.
- Luteolin is associated with potential therapeutic effects in neurological, immune, and metabolic disorders, as well as multiple tumors.

## Abstract

This study employs bibliometric and network pharmacology methods to systematically analyze the development trends, knowledge structure, and potential biological mechanisms of luteolin research from 2000 to 2025, providing insights for its application in nutritional health and disease prevention.

Based on the Web of Science Core Collection (WoSCC), combined with Bibliometrix, VOSviewer, and citespace, we conducted analyses of publication characteristics, keywords, journals, and co-citation networks. Simultaneously, integrating TM-MC, string, and Cytoscape, we constructed a luteolin target-pathway-disease network and performed core target and KEGG enrichment analyses.

Luteolin research exhibits sustained growth, with a significant increase after 2021. Research focus has expanded from early antioxidant and anti-inflammatory mechanisms to metabolic health, immune regulation, tumor suppression, and multisystem protection. Network pharmacology identified 239 potential targets, with core targets including TP53, TNF, STAT3, and EGFR, significantly enriched in p53, PI3K–Akt, TNF, and IL-17 pathways. Disease association networks indicate luteolin’s potential to intervene in neurological, circulatory, metabolic, immune, digestive, respiratory disorders, and multiple tumors, exhibiting typical multi-target comprehensive regulatory characteristics.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], TNF (tumor necrosis factor) [NCBI Gene 7124], STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774], EGFR (epidermal growth factor receptor) [NCBI Gene 1956]
- **Chemicals:** luteolin (PubChem CID 5280445)

## Full-text entities

- **Genes:** IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** , respiratory disorders (MESH:D012131), tumor (MESH:D009369), inflammatory (MESH:D007249)
- **Chemicals:** luteolin (MESH:D047311)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12890652/full.md

## References

74 references — full list in the complete paper: https://tomesphere.com/paper/PMC12890652/full.md

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Source: https://tomesphere.com/paper/PMC12890652