Evidence map›Paper›PMID 41652272›Full record

ArticleJournal of natural medicines2026

Total flavonoids from Carthamus tinctorius L. inhibit the liver fibrosis progression via Hippo/YAP pathway.

Xiaomei Bao, Xiaolu Zhao, Haisheng Wang, Hongwei Yuan, Rong Jin, Mingqi Li, Yinghe Wang, Yuehong Ma

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of natural medicines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Total Flavonoids fromInternational journal of molecular sciences · 2026
    Article
  2. Review
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.

Xiaomei Bao *College of Pharmacy, Inner Mongolia Medical University, Hohhot, China.
Xiaolu Zhao *School of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot, 010010, China.
Haisheng WangSchool of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot, 010010, China.
Hongwei YuanSchool of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot, 010010, China.
Rong JinSchool of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot, 010010, China.
Mingqi LiSchool of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot, 010010, China.
Yinghe WangSchool of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot, 010010, China.
Yuehong MaSchool of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot, 010010, China. myh19982002@sina.com.ORCID http://orcid.org/0000-0003-1414-0066

Funding

Inner Mongolia Talent Development Fund 22056Inner Mongolia University of Science and Technology YKD2023MS072Key Project of Inner Mongolia Medical University YKD2022ZD019National Natural Science Foundation of China 81960759National Natural Science Foundation of China 82460819Natural Science Foundation of Inner Mongolia Autonomous Region 2019MS08010Natural Science Foundation of Inner Mongolia Autonomous Region 2024LHMS08029Natural Science Foundation of Inner Mongolia Autonomous Region of China 2023MS08043Scientific and Technological Innovation Team of Inner Mongolia Medical University on the Anti-Liver Fibrosis Effect of Mongolian Medicine YKD2022TD039
6 · The paper itself

Abstract

Liver fibrosis is a significant global health threat, and Carthamus tinctorius L., a traditional herb used for liver ailments, contains flavonoids with diverse pharmacological properties. This study explored the effects and mechanisms of total flavonoids from Carthamus tinctorius L. (TFCTL) on hepatic fibrosis in mice and TGF-β1-induced activation of hepatic stellate cells (HSCs). Using LC-MS/MS, TFCTL's composition was characterized, and models of liver fibrosis in mice and HSC-T6 cell activation in vitro were established. Techniques such as CCK-8, Western blotting, RT-qPCR, and immunofluorescence revealed that TFCTL inhibited HSC-T6 activation and proliferation by promoting YAP phosphorylation and degradation via increased MST1 and LATS1 expression, suppressing Hippo pathway target genes. TFCTL also improved liver fibrosis pathology in mice, primarily through the Hippo/YAP pathway. These results underscore the anti-fibrotic potential of TFCTL, establishing it as a highly promising candidate for the treatment of liver fibrosis.

Indexed as

Adaptor Proteins, Signal TransducingCarthamus tinctoriusFlavonoidsLiver CirrhosisProtein Serine-Threonine KinasesAnimalsCell LineCell ProliferationHepatic Stellate CellsHippo Signaling PathwayMaleMiceMice, Inbred C57BLSignal TransductionTranscription FactorsTransforming Growth Factor beta1Adaptor Proteins, Signal TransducingFlavonoidsProtein Serine-Threonine KinasesTranscription FactorsTransforming Growth Factor beta1Yap1 protein, mouseYAP-Signaling ProteinsHepatic fibrosisHepatic stellate cellsHippo/YAPTotal flavonoids from Carthamus tinctorius L.

Identifiers

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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.