Evidence map›Paper›PMID 39582546›Full record

ArticleFrontiers in oncology2024

Mechanism of luteolin against non-small-cell lung cancer: a study based on network pharmacology, molecular docking, molecular dynamics simulation, and

Jihang Zhang, Changling Li, Wenyi Li, Zhenpeng Shi, Zhenguo Liu, Junyu Zhou, Jing Tang, Zixuan Ren, Yun Qiao, Deshan Liu

Abstract read
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Integrated Network Pharmacology and Molecular Dynamics Reveal Luteolin fromInternational journal of molecular sciences · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Exploration of the Mechanism of Action ofJournal of hepatocellular carcinoma · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Jihang ZhangThe First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Changling LiDepartment of Traditional Chinese Medicine, Qilu Hospital of Shandong University, Jinan, China.
Wenyi LiThe First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Zhenpeng ShiThe First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Zhenguo LiuThe First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Junyu ZhouThe First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Jing TangThe First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Zixuan RenThe First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Yun QiaoDepartment of Traditional Chinese Medicine, Qilu Hospital of Shandong University, Jinan, China.
Deshan LiuDepartment of Traditional Chinese Medicine, Qilu Hospital of Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Luteolin, a naturally occurring flavonoid compound, demonstrates promising anti-cancer properties. However, its mechanism against non-small-cell lung cancer (NSCLC) remains unknown. This study employed network pharmacology, molecular docking, molecular dynamics simulation (MDS), and Methods: Initially, the potential targets of luteolin and NSCLC-related targets were identified from public databases such as TCMSP, GeneCards, OMIM, DrugBank, and TTD. Subsequently, the protein-protein interaction (PPI) network screening and Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were conducted. The binding affinity and stability of luteolin with the core targets were assessed using molecular docking and MDS. Finally, the results were validated by Results: A total of 56 luteolin targets and 2145 NSCLC-related targets were identified. Six core targets, TP53, EGFR, AKT1, TNF, JUN, and CASP3, were screened via the PPI network. The GO and KEGG analyses indicated that luteolin's activity against NSCLC potentially involves PI3K-Akt, NF-kappa B, and other signaling pathways. Molecular docking revealed that luteolin had high binding affinity with the core targets. MDS confirmed the stable interaction between luteolin and key proteins TP53 and AKT1. Conclusion: Luteolin had a good anti-NSCLC effect, and the apoptosis-inducing effect might be related to the Akt/MDM2/p53 signaling pathway.

Indexed as

Akt/MDM2/p53 signaling pathwayin vitro experimentsluteolinnetwork pharmacologynon-small-cell lung cancer

Identifiers

PMID39582546
PMCPMC11582065

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.