Evidence map›Paper›PMID 37368176›Full record

ArticleApoptosis : an international journal on programmed cell death2023

Neutrophil extracellular traps mediate TLR9/Merlin axis to resist ferroptosis and promote triple negative breast cancer progression.

Linli Yao, Xiaonan Sheng, Xinrui Dong, Weihang Zhou, Ye Li, Xueyun Ma, Yonggang Song, Huijuan Dai, Yueyao Du

Abstract read
PubMed Publisher
In one paragraph

Article in Apoptosis : an international journal on programmed cell death, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

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

9 authors at 4 institutions in 1 country.

Linli Yao *State Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute, School of Medicine, Ren Ji Hospital, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Xiaonan Sheng *Department of Breast Surgery, School of Medicine, Renji Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.
Xinrui Dong *Department of Breast Surgery, School of Medicine, Renji Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.
Weihang ZhouDepartment of Breast Surgery, School of Medicine, Renji Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.
Ye LiDepartment of Breast Surgery, School of Medicine, Renji Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.
Xueyun MaInstitute of Biomedical Sciences, East China Normal University, Shanghai, People's Republic of China.
Yonggang SongThe Affiliated Huaian Hospital of Xuzhou Medical University, Huaian, People's Republic of China. syg3609@163.com.
Huijuan DaiDepartment of Breast Surgery, School of Medicine, Renji Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China. daihuijuan1988@163.com.
Yueyao DuDepartment of Breast Surgery, School of Medicine, Renji Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China. duyy0456@163.com.
Renji Hospital · CNEast China Normal University · CNSecond People’s Hospital of Huai’an · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophil and neutrophil extracellular traps (NETs) were reported to be associated with tumor development, but the exact role and concrete mechanisms are still poorly understood, especially in triple negative breast cancer (TNBC). In this study, our results exhibited that NETs formation in TNBC tissues was higher than that in non-TNBC tissues, and NETs formation was distinctly correlated with tumor size, ki67 level and lymph node metastasis in TNBC patients. Subsequent in vivo experiments demonstrated that NETs inhibition could suppress TNBC tumor growth and lung metastasis. Further in vitro experiments uncovered that oncogenic function of NETs on TNBC cells were possibly dependent on TLR9 expression. We also found that neutrophils from peripheral blood of TNBC patients with postoperative fever were prone to form NETs and could enhance the proliferation and invasion of TNBC cells. Mechanistically, we revealed that NETs could interact with TLR9 to decrease Merlin phosphorylation which contributed to TNBC cell ferroptosis resistance. Our work provides a novel insight into the mechanism of NETs promoting TNBC progression and blocking the key modulator of NETs might be a promising therapeutic strategy in TNBC.

Indexed as

Extracellular TrapsFerroptosisTriple Negative Breast NeoplasmsApoptosisCell Line, TumorCell ProliferationHumansNeurofibromin 2NeutrophilsToll-Like Receptor 9Neurofibromin 2TLR9 protein, humanToll-Like Receptor 9FerroptosisNeutrophil extracellular trapsTLR9/Merlin signalingTriple negative breast cancer

Identifiers

PMID37368176
OpenAlexW4382182311

What OpenQuestion holds

Textmetadata
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.