Evidence map›Paper›PMID 30696442›Full record

ArticleRespiratory research2019

NLRP3 deletion inhibits inflammation-driven mouse lung tumorigenesis induced by benzo(a)pyrene and lipopolysaccharide.

Li Huang, Shuyin Duan, Hua Shao, Aihua Zhang, Shuang Chen, Peng Zhang, Na Wang, Wei Wang, Yongjun Wu, Jing Wang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Therapeutic Significance of NLRP3 Inflammasome in Cancer: Friend or Foe?International journal of molecular sciences · 2024
    Review
  4. Article
  5. Review
  6. Pyroptosis: A promising target for lung cancer therapy.Chinese medical journal pulmonary and critical care medicine · 2023
    Review
  7. Review
  8. Article
  9. Article
  10. Long-term exposure to house dust mites accelerates lung cancer development in mice.Journal of experimental & clinical cancer research : CR · 2023
    Article
  11. Article
  12. Benzo[Frontiers in immunology · 2023
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. 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

14 authors at 5 institutions in 1 country.

Li HuangDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Shuyin DuanDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Hua ShaoDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Aihua ZhangDepartment of Nephrology, the Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Shuang ChenInstitute of Pediatrics, Nanjing Medical University, Nanjing, Jiangsu, China.
Peng ZhangDepartment of Bone and Soft Tissue Cancer, Cancer, the Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), Zhengzhou, Henan, China.
Na WangDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Wei WangDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Yongjun WuDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Jing WangDepartment of Pulmonary Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Hong LiuDepartment of Pulmonary Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Wu YaoDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Qiao ZhangDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China.
Feifei FengDepartment of Toxicology, College of Public Health, Zhengzhou University, No.100 Kexue Avenue, Zhengzhou, 450001, Henan province, China. feifeifeng@zzu.edu.cn.
Zhengzhou University · CNFirst Affiliated Hospital of Zhengzhou University · CNHenan Cancer Hospital · CNNanjing Medical University · CNSecond Affiliated Hospital of Nanjing Medical University · CN

Funding

the grant from Henan Department of Education 14A330001the grants from Henan Department of Science and Technology, China 162102310319the grants from Henan Department of Science and Technology, China 162102310602the National Natural Science Foundation of China 81402712the outstanding youth grant of Zhengzhou University 1421329082the program of scientific and technological innovation talents of Henan Province 154200510015the training grant of Zhengzhou University 2017ZDGGJS039
6 · The paper itself

Abstract

backgroundInflammatory micro-environment has been proposed to play a critical role in lung tumorigenesis. NLRP3 is known as an intracellular receptor involving inflammation and has been reported which is increasingly associated with tumor development, but the role in inflammation-driven lung cancer has not been fully clarified. In this study, we investigated whether lipopolysaccharide (LPS)-induced pulmonary inflammation could contribute to lung tumorigenesis induced by benzo(a)pyrene [B(a)p] in C57BL/6J mice and the role of NLRP3 in the pathogenesis.

methodsNLRP3-/- mice and C57BL/6J mice (wide-type, WT) were instilled intratracheally with B(a)p (1 mg/mouse) once a week for 4 times [the week of the last time of B(a)p treatment named Week 0], and mice were then instilled intratracheally with LPS at Week 3, 2.5 μg/mouse, once every three weeks for 5 times. At Week 30, the incidence, number, size and histopathology of lung tumor were analyzed.

resultsMice exposed to B(a)p or B(a)p plus LPS could induce lung tumors, whereas LPS or vehicles treatment could not induce lung tumorigenesis. In WT mice, B(a)p plus LPS exposure significantly increased tumor incidence, mean tumor count and tumor size of visible tumors of lungs compared with B(a)p treatment alone, and NLRP3 deletion inhibited lung tumorigenesis induced by B(a)p or B(a)p plus LPS. Histopathological examination found LPS-induced pulmonary inflammatory changes enhanced lung tumorigenesis induced by B(a)p in WT mice, deletion of NLRP3 improved the inflammatory changes induced by LPS and the number and size of pathological tumor nests induced by B(a)p or B(a)p plus LPS. In addition, we found B(a)p treatment and B(a)p plus LPS treatment predominately induced the development of adenoma.

conclusionLPS enhanced B(a)p-induced lung tumorigenesis in WT and NLRP3-/- mice of C57BL/6J strain, and NLRP3 deletion inhibits lung tumorigenesis induced by B(a)p or B(a)p plus LPS.

Indexed as

AnimalsBenzo(a)pyreneCarcinogenesisFemaleLipopolysaccharidesLung NeoplasmsMaleMiceMice, Inbred C57BLMice, KnockoutNLR Family, Pyrin Domain-Containing 3 ProteinBenzo(a)pyreneLipopolysaccharidesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseBenzo(a)pyreneInflammationLipopolysaccharideLung tumorigenesisNLRP3

Identifiers

PMID30696442
PMCPMC6352353
OpenAlexW2919988733

What OpenQuestion holds

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LicenceCC BY
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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.