Evidence map›Paper›PMID 35399564›Full record

ArticleTranslational lung cancer research2022

CircP4HB regulates ferroptosis via SLC7A11-mediated glutathione synthesis in lung adenocarcinoma.

Chun-Feng Pan, Ke Wei, Zi-Jian Ma, Yao-Zhou He, Jing-Jing Huang, Zi-Zhang Guo, Zhi-Peng Chen, Martin P Barr, Rodney E Shackelford, Yang Xia and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Translational lung cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
9.9field-weighted citation impact, top 1% of its field
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

37 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  10. Genetic profile of ferroptosis in non-small cell lung carcinoma and pharmaceutical options for ferroptosis induction.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  11. Review
  12. CircDUSP22 Attenuates the Ferroptosis of Prostate Cancer CellsCombinatorial chemistry & high throughput screening · 2025
    Article
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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

11 authors at 3 institutions in 3 countries.

Chun-Feng Pan *Department of Thoracic Surgery, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Ke Wei *Department of Thoracic Surgery, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Zi-Jian Ma *Department of Thoracic Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Yao-Zhou HeDepartment of Oncology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Jing-Jing HuangDepartment of Thoracic Surgery, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Zi-Zhang GuoDepartment of Thoracic Surgery, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Zhi-Peng ChenDepartment of Thoracic Surgery, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Martin P BarrThoracic Oncology Research Group, School of Medicine, Trinity Translational Medicine Institute, Trinity Centre for Health Sciences, St. James's Hospital and Trinity College Dublin, Dublin, Ireland.
Rodney E ShackelfordDepartment of Pathology, LSU Health Shreveport, Shreveport, LA, USA.
Yang XiaDepartment of Thoracic Surgery, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Jun WangDepartment of Thoracic Surgery, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNLouisiana State University Health Sciences Center Shreveport · USTrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Circular ribonucleic acids (circRNAs) play a key role in the development of different types of cancer. Ferroptosis is a type of programmed cell death that contributes to cancer progression. However, the role of circRNAs in lung adenocarcinoma (LUAD) ferroptosis remains unclear. Methods: The gene expression levels of circRNA P4HB (circP4HB), microRNA-1184 (miR-1184) and Solute carrier family 7 member 11 ( Results: CircP4HB expression levels were increased in LUAD. It triggered glutathione (GSH) synthesis and, therefore protected LUAD cells from ferroptosis induced by erastin. CircP4HB may function as a competing endogenous RNA by modulating miR-1184 to regulate SLC7A11. CircP4HB inhibited ferroptosis by regulating miR-1184/ SLC7A11-mediated GSH synthesis. In vivo, overexpression of circP4HB promoted tumor growth and inhibited ferroptosis. Conclusions: The circRNA, circP4HB acts as a novel ferroptosis suppressor in LUAD. Furthermore, circP4HB protects LUAD from ferroptosis via modulation of the miR-1184/SLC7A11 axis. Our findings identified circP4HB as a novel biomarker in LUAD and warrants further investigation in the early diagnosis and treatment of LUAD.

Indexed as

Circular ribonucleic acids (circRNAs)glutathione (GSH)lung adenocarcinoma (LUAD)miR-1184SLC7A11

Identifiers

PMID35399564
PMCPMC8988082
OpenAlexW4214689105

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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.