Evidence map›Paper›PMID 19654875›Full record

ArticlePloS one2009

Blocking TLR2 activity attenuates pulmonary metastases of tumor.

Hong-Zhen Yang, Bing Cui, Han-Zhi Liu, Su Mi, Jun Yan, Hui-Min Yan, Fang Hua, Heng Lin, Wen-Feng Cai, Wen-Jie Xie and 5 more

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. The HSP Immune Network in Cancer.Frontiers in immunology · 2021
    Review
  11. Review
  12. Review
  13. Exposition to Biological Control AgentFrontiers in cellular and infection microbiology · 2020
    Article
  14. Association between small intestinal bacterial overgrowth and toll-like receptor 4 in patients with pancreatic carcinoma and cholangiocarcinoma.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2019
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Molecular mechanisms involved in dendritic cell dysfunction in cancer.Cellular and molecular life sciences : CMLS · 2017
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Hong-Zhen YangMolecular Immunology and Pharmacology Laboratory, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Bing Cui
Han-Zhi Liu
Su Mi
Jun Yan
Hui-Min Yan
Fang Hua
Heng Lin
Wen-Feng Cai
Wen-Jie Xie
Xiao-Xi Lv
Xiao-Xing Wang
Bing-Mu Xin
Qi-Min Zhan
Zhuo-Wei Hu
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastasis is the most pivotal cause of mortality in cancer patients. Immune tolerance plays a crucial role in tumor progression and metastasis. METHODS AND

findingsIn this study, we investigated the potential roles and mechanisms of TLR2 signaling on tumor metastasis in a mouse model of intravenously injected B16 melanoma cells. Multiple subtypes of TLRs were expressed on B16 cells and several human cancer cell lines; TLR2 mediated the invasive activity of these cells. High metastatic B16 cells released more heat shock protein 60 than poor metastatic B16-F1 cells. Importantly, heat shock protein 60 released by tumor cells caused a persistent activation of TLR2 and was critical in the constitutive activation of transcription factor Stat3, leading to the release of immunosuppressive cytokines and chemokines. Moreover, targeting TLR2 markedly reduced pulmonary metastases and increased the survival of B16-bearing mice by reversing B16 cells induced immunosuppressive microenvironment and restoring tumor-killing cells such as CD8(+) T cells and M1 macrophages. Combining an anti-TLR2 antibody and a cytotoxic agent, gemcitabine, provided a further improvement in the survival of tumor-bearing mice. CONCLUSIONS AND SIGNIFICANCE: Our results demonstrate that TLR2 is an attractive target against metastasis and that targeting immunosuppressive microenvironment using anti-TLR2 antibody is a novel therapeutic strategy for combating a life-threatening metastasis.

Indexed as

AnimalsChaperonin 60ChemokinesCytokinesLung NeoplasmsMelanoma, ExperimentalMiceNeoplasm MetastasisToll-Like Receptor 2Chaperonin 60ChemokinesCytokinesTlr2 protein, mouseToll-Like Receptor 2

Identifiers

PMID19654875
PMCPMC2716531
OpenAlexW2124310819

What OpenQuestion holds

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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.