Evidence map›Paper›PMID 42983275›Full record

ArticleBiological procedures online2026

Fuzheng Yiai Formula and its Key Components Inhibited PCa by TP53/SLC7A11/GPX4-Induced Ferroptosis.

Wen Sheng, Yingqiu Li, Xiaopeng Yu, Xiaoke Zeng, Yujie Jiang, Qingting Wu, Fanshun Shen, Xiye Ouyang, Qinghu He

Abstract read
In one paragraph

Article in Biological procedures online, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Wen ShengSchool of Traditional Chinese Medicine, Hunan University of Medicine, No. 492 Jinxi South Road, Huaihua, 418000, China.
Yingqiu LiMedical School, Hunan University of Chinese Medicine, Changsha, 410208, China.
Xiaopeng YuAndrology Laboratory, Hunan University of Chinese Medicine, Changsha, 410208, China.
Xiaoke ZengSchool of Traditional Chinese Medicine, Hunan University of Medicine, No. 492 Jinxi South Road, Huaihua, 418000, China.
Yujie JiangSchool of Traditional Chinese Medicine, Hunan University of Medicine, No. 492 Jinxi South Road, Huaihua, 418000, China.
Qingting WuSchool of Traditional Chinese Medicine, Hunan University of Medicine, No. 492 Jinxi South Road, Huaihua, 418000, China.
Fanshun ShenHunan Chunguang Jiuhui Modern Chinese Medicine Co., Ltd., Liuyang, 410300, China.
Xiye OuyangHunan Chunguang Jiuhui Modern Chinese Medicine Co., Ltd., Liuyang, 410300, China.
Qinghu HeSchool of Traditional Chinese Medicine, Hunan University of Medicine, No. 492 Jinxi South Road, Huaihua, 418000, China. qinghu_he3418@hnucm.edu.cn.ORCID https://orcid.org/0000-0003-0838-2720

Funding

Doctoral Scientific Research Starting Foundation of Hunan University of Medicine 202409Hunan Provincial Furong Plan Young Talents for Science and Technology Innovation 2025RC3217Key Project of Hunan Provincial Department of Education 24A0765Natural Science Foundation of Hunan Province 2025JJ70415
6 · The paper itself

Abstract

Fuzheng Yiai Formula (FZYAF) is a traditional Chinese medicine compound, and its key components, ursolic acid (UA) and Anhydroicaritin (AHI), have potential antitumor activity, but their mechanisms of action in Prostate cancer (PCa) remain unclear.Key components and targets of FZYAF were identified by network pharmacology, and the components were further validated by HPLC-MS analysis. PCa cells were treated with UA and AHI to assess their effects on cell proliferation, migration, and ferroptosis. The interaction of UA or AHI with TP53 was assessed by molecular docking and DARTS. In vivo, a PCa mouse model was established, and tumor tissues from FZYAF-treated mice were subjected to metabolomic analysis. Additionally, the anti-tumor effects of FZYAF, UA, and AHI, and their impact on ferroptosis and the TP53 pathway were evaluated.Network pharmacology and HPLC-MS analysis, UA and AHI were identified as the key active components of FZYAF, and TP53 was predicted as a core target. In vitro, UA and AHI inhibited PCa cell proliferation and migration and induced ferroptosis, with their combination showing enhanced efficacy compared to either agent alone. Mechanistically, UA and AHI were bound to and upregulated the TP53 protein. In vivo, FZYAF inhibited tumor growth and induced ferroptosis in PCa mice, which was associated with alterations in lipid metabolism-related pathways, as revealed.UA and AHI, key components of FZYAF, inhibit PCa progression by binding to and upregulating the TP53 protein to induce ferroptosis. This study elucidates the role of FZYAF in developing anti-PCa drugs.

Indexed as

AnhydroicaritinFuzheng Yiai FormulaProstate CancerTP53Ursolic Acid

Identifiers

PMID42983275
PMCPMC13732933

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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.