Evidence map›Paper›PMID 38769295›Full record

ArticleNature communications2024

Targeting SOX13 inhibits assembly of respiratory chain supercomplexes to overcome ferroptosis resistance in gastric cancer.

Hui Yang, Qingqing Li, Xingxing Chen, Mingzhe Weng, Yakai Huang, Qiwen Chen, Xiaocen Liu, Haoyu Huang, Yanhuizhi Feng, Hanyu Zhou and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

  1. Article
  2. Targeting ferroptosis to overcome drug resistance in gastrointestinal cancers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

21 authors.

Hui Yang *Central Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.ORCID http://orcid.org/0000-0002-3938-9530
Qingqing Li *Anhui Province Key Laboratory of Non-coding RNA Basic and Clinical Transformation, Wuhu, Anhui, China.ORCID http://orcid.org/0000-0002-9115-3621
Xingxing Chen *Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0003-1759-3159
Mingzhe Weng *Department of General Surgery, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.ORCID http://orcid.org/0000-0002-4856-7925
Yakai Huang *Department of Gastric Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Qiwen ChenMinimally Invasive Therapy Center, Department of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xiaocen LiuAnhui Province Key Laboratory of Non-coding RNA Basic and Clinical Transformation, Wuhu, Anhui, China.ORCID http://orcid.org/0000-0002-7420-9670
Haoyu HuangCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.
Yanhuizhi FengDepartment of Implantology, Stomatological Hospital and Dental School of Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai, 200072, China.
Hanyu ZhouCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.ORCID http://orcid.org/0000-0003-2419-1780
Mengying ZhangCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.
Weiya PeiCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.
Xueqin LiCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.
Qingsheng FuDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.ORCID http://orcid.org/0000-0003-1933-1654
Liangyu ZhuCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.ORCID http://orcid.org/0000-0001-6804-0349
Yingying WangDepartment of Nuclear Medicine, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.
Xiang KongCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China.ORCID http://orcid.org/0000-0003-1734-5171
Kun LvCentral Laboratory, The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College), Wuhu, Anhui, China. lvkun315@126.com.ORCID http://orcid.org/0000-0002-1895-6700
Yan ZhangAnhui Province Key Laboratory of Non-coding RNA Basic and Clinical Transformation, Wuhu, Anhui, China. yanyan0921@sina.com.ORCID http://orcid.org/0000-0001-8843-6156
Yangbai SunDepartment of Musculoskeletal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China. drsunyb@fudan.edu.cn.
Mingzhe MaDepartment of Gastric Surgery, Fudan University Shanghai Cancer Center, Shanghai, China. mmz666@163.com.ORCID http://orcid.org/0000-0001-8858-0983

Funding

Natural Science Foundation of Shanghai (Natural Science Foundation of Shanghai Municipality) 22ZR1412700
6 · The paper itself

Abstract

Therapeutic resistance represents a bottleneck to treatment in advanced gastric cancer (GC). Ferroptosis is an iron-dependent form of non-apoptotic cell death and is associated with anti-cancer therapeutic efficacy. Further investigations are required to clarify the underlying mechanisms. Ferroptosis-resistant GC cell lines are constructed. Dysregulated mRNAs between ferroptosis-resistant and parental cell lines are identified. The expression of SOX13/SCAF1 is manipulated in GC cell lines where relevant biological and molecular analyses are performed. Molecular docking and computational screening are performed to screen potential inhibitors of SOX13. We show that SOX13 boosts protein remodeling of electron transport chain (ETC) complexes by directly transactivating SCAF1. This leads to increased supercomplexes (SCs) assembly, mitochondrial respiration, mitochondrial energetics and chemo- and immune-resistance. Zanamivir, reverts the ferroptosis-resistant phenotype via directly targeting SOX13 and promoting TRIM25-mediated ubiquitination and degradation of SOX13. Here we show, SOX13/SCAF1 are important in ferroptosis-resistance, and targeting SOX13 with zanamivir has therapeutic potential.

Indexed as

Drug Resistance, NeoplasmFerroptosisStomach NeoplasmsAnimalsCell Line, TumorElectron TransportGene Expression Regulation, NeoplasticHumansMiceMitochondriaMolecular Docking SimulationUbiquitin-Protein LigasesUbiquitin-Protein Ligases

Identifiers

PMID38769295
PMCPMC11106335

What OpenQuestion holds

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LicenceCC BY
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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.