Evidence map›Paper›PMID 39991627›Full record

ReviewMedComm2025

Ferroptosis in Pulmonary Disease and Lung Cancer: Molecular Mechanisms, Crosstalk Regulation, and Therapeutic Strategies.

Dandan Guo, Songhua Cai, Lvdan Deng, Wangting Xu, Sentao Fu, Yaling Lin, Tong Jiang, Qing Li, Zhijun Shen, Jian Zhang and 3 more

Abstract readReview
In one paragraph

Review in MedComm, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

13 authors.

Dandan GuoThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
Songhua CaiDepartment of Thoracic Surgery National Cancer Center National Clinical Research Center for Cancer Cancer Hospital & Shenzhen Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Shenzhen Guangdong China.
Lvdan DengThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
Wangting XuDepartment of Respiratory First Affiliated Hospital School of Medicine Zhejiang University Hangzhou Zhejiang China.
Sentao FuThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
Yaling LinThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
Tong JiangThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
Qing LiThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
Zhijun ShenThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
Jian ZhangThe Department of Oncology Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
Peng LuoThe Department of Oncology Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
Bufu TangDepartment of Radiation Oncology Zhongshan Hospital Fudan University Shanghai Shanghai China.
Ling WangThe Department of Oncology First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.ORCID https://orcid.org/0000-0002-5176-7469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is a distinct form of iron-dependent programmed cell death characterized primarily by intracellular iron accumulation and lipid peroxidation. Multiple cellular processes, including amino acid metabolism, iron metabolism, lipid metabolism, various signaling pathways, and autophagy, have been demonstrated to influence the induction and progression of ferroptosis. Recent investigations have elucidated that ferroptosis plays a crucial role in the pathogenesis of various pulmonary disorders, including lung injury, chronic obstructive pulmonary disease, pulmonary fibrosis, and asthma. Ferroptosis is increasingly recognized as a promising novel strategy for cancer treatment. Various immune cells within the tumor microenvironment, including CD8+ T cells, macrophages, regulatory T cells, natural killer cells, and dendritic cells, have been shown to induce ferroptosis in tumor cells and modulate the process through the regulation of iron and lipid metabolism pathways. Conversely, ferroptosis can reciprocally alter the metabolic environment, leading to the activation or inhibition of immune cell functions, thereby modulating immune responses. This paper reviews the molecular mechanism of ferroptosis and describes the tumor immune microenvironment, discusses the connection between ferroptosis and the tumor microenvironment in lung cancer and pulmonary diseases, and discusses the development prospect of their interaction in the treatment of lung cancer and pulmonary diseases.

Indexed as

ferroptosisimmune microenvironmentlung cancermolecular mechanismspulmonary disease

Identifiers

PMID39991627
PMCPMC11847630

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.