Evidence map›Paper›PMID 41447430›Full record

ArticleDiscover oncology2025

CTHRC1/TGF-β/Smad axis serves as therapeutic targets in inhibiting oral squamous cell carcinoma by mediating ferroptosis.

Shihao Huang, Yiming Jiao, Yongchun Chang, Yu Feng, Guixian Mu, Linli Xie

Abstract read
In one paragraph

Article in Discover oncology, 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

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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

1 citing paper in PubMed.

  1. 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

6 authors.

Shihao HuangAcupuncture and Tuina Academy, Beijing University of Chinese Medicine, Beijing, 100029, China.
Yiming JiaoDepartment of Acupuncture, Dongguan Affiliated Hospital of Guangzhou, University of Chinese Medicine, Dongguan, 523000, Guangdong, China.
Yongchun ChangDepartment of Stomatology, Jinan Shizhong District People's Hospital, Jinan, 250002, Shandong, China.
Yu FengDepartment of Nephrology and Endocrinology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, 100000, China.
Guixian MuSchool of Public Health, Shandong Second Medical University, Weifang, 261000, Shandong, China.
Linli XieDepartment of Traditional Chinese Medicine Internal Medicine, Huguosi Traditional Chinese Medicine Hospital, Beijing University of Chinese Medicine, No. 83 Cotton Hutong, Beijing, 100035, China. linlixie1979@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCollagen triple helix repeat containing 1 (CTHRC1) is an oncogene in numerous human cancers including oral squamous cell carcinoma (OSCC). However, whether and how CTHRC1 influences OSCC progression through ferroptosis has not been completely clarified.

methodsqRT-PCR were conducted to assess CTHRC1 expression in OSCC. The proliferation of OSCC cells were assessed through 5-ethynyl-2'-deoxyuridine (EdU) assay, colony formation, and CCK-8 assays. Flow cytometry was used to analyze the apoptotic cells of OSCC cells. Ferroptosis was assessed based on the amounts of MDA, lipid ROS, intracellular Fe

resultsPronounced overexpression of CTHRC1 was observed in OSCC cell lines (SCC-9, CAL-27 and SCC-25). Knockdown CTHRC1 overtly inhibited cell proliferation but induced apoptosis in OSCC cells. Moreover, silencing of CTHRC1 could stimulate ferroptosis, as well as inhibit the activation of TGF-β/Smad pathway. Treatment with SRI-011381, a TGF-β/Smad pathway specific agonist, significantly reversed the promoting effect of CTHRC1 silencing on ferroptosis in OSCC cells.

conclusionsOur findings indicate that knockdown of CTHRC1 stimulates ferroptosis in OSCC through inhibiting TGF-β/Smad pathway, which provides important experimental data and theoretical basis for the management, diagnosis, and treatment of OSCC.

Indexed as

CTHRC1FerroptosisOral squamous cell carcinomaTGF-β/Smad

Identifiers

PMID41447430
PMCPMC12847467

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