Evidence map›Paper›PMID 40473597›Full record

ArticleCell death & disease2025

Circular RNA TFRC/SCD1 mRNA interaction regulates ferroptosis and metastasis in gastric cancer.

Zhi Lin, Chonglei Zhong, Ming Shi, Qinpeng Long, Liang Jing, Yang Yu, Jing Chou, Miao Chen, Minhuan Lan, Fei Long

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

10 authors.

Zhi Lin *Department of Pediatrics, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
Chonglei Zhong *Department of Gastrointestinal Surgery, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
Ming ShiDepartment of Gastrointestinal Surgery, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
Qinpeng LongDepartment of Pediatrics, The First Affiliated Hospital of University of South China, Hengyang, Hunan, China.
Liang JingDepartment of Gastrointestional Surgery, Hunan University of Medicine General Hospital, Huaihua, Hunan, China.
Yang YuDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, Guangzhou, Guangdong, China.
Jing ChouDepartment of Gastrointestinal Surgery, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
Miao ChenDepartment of Gastrointestinal Surgery, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
Minhuan LanCollege of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan, China.
Fei LongDepartment of Gastrointestinal Surgery, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China. 984210652@qq.com.ORCID http://orcid.org/0000-0003-4698-9822

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82303255National Natural Science Foundation of China (National Science Foundation of China) 82400213
6 · The paper itself

Abstract

Ferroptosis, an iron-dependent form of programmed cell death, holds promise for cancer treatment. Circular RNAs (circRNAs), widely expressed across tumor types, modulate multiple cellular biological processes, including ferroptosis. However, the regulatory dynamics of circRNAs in gastric cancer (GC)-associated ferroptosis remain poorly understood. Here, circTFRC (circBase ID: hsa_circ_0068606), a novel circRNA, was identified as significantly upregulated in GC tissues and cell lines, with its plasma levels strongly associated with tumor size and metastatic status. Targeted suppression of circTFRC enhanced ferroptotic cell death, resulting in reduced proliferation and motility of GC cells in vitro. At the molecular level, circTFRC bound directly to SCD1 mRNAs, stabilizing and enhancing their translation via recruiting the RNA-binding protein ELAVL1. Elevated SCD1 expression mitigated ferroptosis and promoted oncogenic lipid metabolic reprogramming, thereby driving GC progression. In vivo studies further confirmed that circTFRC silencing promoted ferroptosis and inhibited tumor growth and progression. These results delineate a circTFRC-mediated axis that impairs ferroptosis vulnerability in GC cells and supports malignancy advancement. CircTFRC emerges as a biomarker with diagnostic potential and a candidate for therapeutic intervention targeting ferroptosis in GC.

Indexed as

FerroptosisReceptors, TransferrinRNA, CircularRNA, MessengerStearoyl-CoA DesaturaseStomach NeoplasmsAnimalsAntigens, CDCell Line, TumorCell MovementCell ProliferationELAV-Like Protein 1FemaleGene Expression Regulation, NeoplasticHumansMaleAntigens, CDCD71 antigenELAVL1 protein, humanELAV-Like Protein 1Receptors, TransferrinRNA, CircularRNA, MessengerSCD1 protein, humanStearoyl-CoA Desaturase

Identifiers

PMID40473597
PMCPMC12141735

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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.