Evidence map›Paper›PMID 41078164›Full record

ArticleJournal of cellular and molecular medicine2025

Centipede Polypeptide Affects the Inflammatory Reaction and Ferroptosis of Liver Cancer Cells Through the p53/TRAIL Pathway.

Xingru Xing, Linzhu Lu, Zhen Huang, Jiawei Wang, Lihuai Wang, Yuxing Hu, Shan Yin, Sha Tian

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

8 authors.

Xingru XingDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine of Hunan University of Chinese Medicine, Changsha, Hunan, China.ORCID 0009-0006-8293-3331
Linzhu LuDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Zhen HuangDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Jiawei WangDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Lihuai WangThe First Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Yuxing HuDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Shan YinDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Sha TianDepartment of Internal Medicine, College of Integrated Chinese and Western Medicine of Hunan University of Chinese Medicine, Changsha, Hunan, China.

Funding

Chinese Medicine Scientific Research Program of Hunan Province 2021235Excellent Youth Program of Hunan Provincial Education Department 21B0384Natural Science Foundation of Hunan Province 2021JJ40405Regional Joint Fund of Natural Science Foundation of Hunan Province 2025JJ70640Scientific Research Programme of Hunan Provincial Health and Wellness Commissio B202319017574
6 · The paper itself

Abstract

Various extracts from centipedes have therapeutic effects on liver cancer. This study aims to illustrate the impact and mechanism of centipede polypeptide (CP) on liver cancer. The suitable CP concentration and liver cancer cells were screened through CCK-8 analysis. The expression of proteins was analysed by Western blot. The level of cytokines and markers was measured by ELISA and biochemical kits. The apoptosis rate of cells was analysed by TUNEL staining and flow cytometry. Histopathological changes were observed by HE staining. The expression of Ki-67 and caspase-3 was assessed by IHC staining. The combination of CP and p53 was simulated by molecular docking. 200 μg/mL CP and HepG2 cells were applied in experiments. CP significantly upregulated p53, TNF-associated apoptosis-inducing ligand (TRAIL), TRADD and TRAF expression in HepG2 cells and tumour tissues (p < 0.05), suggesting p53-dependent activation of the TRAIL pathway. CP raised the levels of IL-6, IL-1β, TNF-α, MDA and ROS, and decreased those of IL-10, TGF-β1 and SOD in HepG2 cell supernatant and serum of nude mice (p < 0.05). CP promoted cell apoptosis and reduced the levels of ALT and AST to inhibit the progression of cancer. Molecular docking showed that CP could bind stably to p53 (p < 0.05). Silencing of p53 restrained the activation of the p53/TRAIL pathway and reduced the level of inflammatory reaction and ferroptosis, thus reversing the therapeutic effect of CP on liver cancer (p < 0.05). CP affected the inflammatory reaction and ferroptosis of liver cancer cells through the p53/TRAIL pathway.

Indexed as

FerroptosisInflammationLiver NeoplasmsPeptidesSignal TransductionTNF-Related Apoptosis-Inducing LigandTumor Suppressor Protein p53AnimalsApoptosisHep G2 CellsHumansMaleMiceMice, NudeMolecular Docking SimulationPeptidesTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanTP53 protein, humanTumor Suppressor Protein p53centipede polypeptideferroptosisinflammatory reactionliver cancerp53/TRAIL pathway

Identifiers

PMID41078164
PMCPMC12516244

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Registered trials

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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.