Evidence map›Paper›PMID 40822624›Full record

ArticleCytotechnology2025

Salidroside alleviates the progression of idiopathic pulmonary fibrosis by regulating ferroptosis.

Homood Alharbi, Mohammad Ahmad, Liya Tu, Chunxiao He

Abstract read
In one paragraph

Article in Cytotechnology, 2025. 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. Review
  2. 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

4 authors.

Homood AlharbiDepartment of Medical Surgical Nursing, College of Nursing, King Saud University, 11421 Riyadh, Saudi Arabia.
Mohammad AhmadDepartment of Medical Surgical Nursing, College of Nursing, King Saud University, 11421 Riyadh, Saudi Arabia.
Liya TuDepartment of Pharmacy, Third People's Hospital of Hangzhou, Hangzhou, 310009 Zhejiang China.
Chunxiao HeDepartment of Pharmacy, Third People's Hospital of Hangzhou, Hangzhou, 310009 Zhejiang China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive interstitial pneumonia of unknown etiology, characterized by recurrent acute lung injury. This leads to worsening dyspnea and lung function decline. Patients with idiopathic pulmonary fibrosis (IPF) generally have a poor prognosis, often succumbing within 2-3 years of diagnosis, and the five-year survival rate is below 40%. Analysis of gene differences between raw and normal samples in the database, along with gene ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, suggests that ferroptosis may play a role in the development of pulmonary fibrosis. To test this hypothesis, transforming growth factor beta 1 (TGF-β1) was used to induce fibrosis in vitro, and levels of pulmonary fibrosis markers such as alpha-smooth muscle actin (α-SMA), fibronectin (FSN), and collagen (COL) were measured by enzyme-linked immunosorbent assay (ELISA). The results confirmed successful establishment of the pulmonary fibrosis model in vitro and indicated increased levels of ferroptosis markers, including glutathione (GSH) and iron accumulation. Salidroside, an extract from

Indexed as

FerroptosisIdiopathic pulmonary fibrosisPLA2G4ASalidroside

Identifiers

PMID40822624
PMCPMC12354939

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.