Evidence map›Paper›PMID 24658642›Full record

ArticleCancer biology & therapy2014

Systemic inflammation promotes lung metastasis via E-selectin upregulation in mouse breast cancer model.

Man Jiang, Xiaoya Xu, Yuli Bi, Jiying Xu, Chengyong Qin, Mingyong Han

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Cell-cell communication characteristics in breast cancer metastasis.Cell communication and signaling : CCS · 2024
    Review
  6. Article
  7. Article
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  11. Article
  12. Article
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  15. Article
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  18. Review
  19. Far-reaching effects from carbon nanotubes.Nature nanotechnology · 2019
    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

6 authors at 4 institutions in 1 country.

Man JiangCancer Therapy and Research Center; Shandong Provincial Hospital; Shandong University; Jinan, PR China.
Xiaoya XuCancer Therapy and Research Center; Shandong Provincial Hospital; Shandong University; Jinan, PR China.
Yuli BiCancer Therapy and Research Center; Shandong Provincial Hospital; Shandong University; Jinan, PR China.
Jiying XuCancer Therapy and Research Center; Shandong Provincial Hospital; Shandong University; Jinan, PR China.
Chengyong QinCancer Therapy and Research Center; Shandong Provincial Hospital; Shandong University; Jinan, PR China.
Mingyong HanCancer Therapy and Research Center; Shandong Provincial Hospital; Shandong University; Jinan, PR China.
Shandong Tumor Hospital · CNShandong University · CNShandong First Medical University · CNShandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic inflammation might modulate the microenvironment in the lungs and promotes metastasis. E-selectin, an inflammation inducible endothelial cell adhesion molecule, has been reported to play an important role in homing metastatic cancer cells. To study the effects of E-selectin expression induced by systemic inflammation on breast cancer metastasis, we first treated BALB/c mice with lipopolysaccharide (LPS) to induce systemic inflammation. Pulmonary tissues were analyzed by wet/dry ratio, hematoxylin and eosin (H&E) staining and immunohistochemistry. Then 4T1 cells were injected via tail vein. Lung surface metastasis was counted and detected by histological analysis. LPS-induced E-selectin expression and tumor cells adhesion were assessed by western blotting and immunofluorescence. The circulating levels of proinflammatory cytokines in sera were evaluated by ELISA. Our results showed that a significant increase in breast cancer metastasis to lungs was observed in LPS-treated mice vs. the PBS-treated mice, accompanying with an increased E-selectin expression in pulmonary tissue of LPS-treated mice. In vitro studies showed a significant elevation of E-selectin production in MPVECs which enhanced the adhesion activity of 4T1 cells. Treatment with anti-E-selectin antibody significantly reduced the development of metastasis in vivo, and significantly reduced the adhesion of 4T1 cells to MPVECs in vitro. Our results suggest that systemic inflammation may increase the expression of E-selectin which mediated the lung metastasis of breast cancer in mouse model.

Indexed as

Up-RegulationAnimalsCell AdhesionCell Line, TumorCell ProliferationCoculture TechniquesEndothelium, VascularE-SelectinFemaleGene ExpressionHumansInflammationLipopolysaccharidesLung NeoplasmsMammary Neoplasms, ExperimentalMice, Inbred BALB CE-SelectinLipopolysaccharidesbreast cancerE-selectininflammationLPSlungmetastasismicroenvironment

Identifiers

PMID24658642
PMCPMC4049794
OpenAlexW2073111061

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.