Evidence map›Paper›PMID 22364742›Full record

ArticleMolecular cell2012

IL6-mediated suppression of miR-200c directs constitutive activation of inflammatory signaling circuit driving transformation and tumorigenesis.

Matjaz Rokavec, Weilin Wu, Jun-Li Luo

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
11.3field-weighted citation impact, top 1% 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

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 143 citations in OpenAlex.

  1. Pooled it
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  8. Review
  9. Article
  10. HER2-driven breast cancer suppression by the JNK signaling pathway.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Review
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  13. Article
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  17. Article
  18. Role of Exosomal Non-Coding RNAs in Bone-Related Diseases.Frontiers in cell and developmental biology · 2021
    Review
  19. Epigenetic Signaling of Cancer Stem Cells During Inflammation.Frontiers in cell and developmental biology · 2021
    Review
  20. Review

27 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Matjaz RokavecDepartment of Cancer Biology, The Scripps Research Institute, Jupiter, FL 33458, USA.
Weilin Wu
Jun-Li Luo
Scripps Research Institute · US

Funding

Immune-inflammatory signaling and hormone-refractory prostate cancer evolution.R01CA140956 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI LUO, JUN-LI · 2011 to 2015
$2.0M
NCI NIH HHS 1R01CA140956-01NCI NIH HHS R01 CA140956
6 · The paper itself

Abstract

Abnormal inflammatory signaling activation occurs commonly in cancer cells. However, how it is initiated and maintained and its roles in early stages of tumorigensis are largely unknown. Here, we report that the monocyte-derived MCP-1-induced transformation of immortal breast epithelial cells is triggered by transient activation of MEK/ERK and IKK/NF-κB pathways and maintained by constitutive activation of a feed-forward inflammatory signaling circuit composed of miR-200c, p65, JNK2, HSF1, and IL6. Suppression of miR-200c by IL6 constitutively activates p65/RelA and JNK2, and the latter phosphorylates and activates HSF1. In turn, HSF1 triggers demethylation of the IL6 promoter that facilitates the binding of p65 and c-Jun, which together drive constitutive IL6 transcription. Importantly, this signaling circuit is manifest in human cancer cells and in a mouse model of ErbB2-driven breast cancer, where IL6 loss significantly impairs tumorigenesis. Therefore, targeting this signaling circuit represents an effective therapeutic avenue for breast cancer prevention and treatment.

Indexed as

AnimalsBreastCell Transformation, NeoplasticChemokine CCL2DNA-Binding ProteinsEpithelial CellsEstrogen Receptor alphaFemaleHeat Shock Transcription FactorsHumansInflammationInterleukin-6JNK Mitogen-Activated Protein KinasesMiceMice, TransgenicMicroRNAsCCL2 protein, humanChemokine CCL2DNA-Binding ProteinsESR1 protein, humanEstrogen Receptor alphaHeat Shock Transcription FactorsHsf1 protein, mouseInterleukin-6JNK Mitogen-Activated Protein KinasesMicroRNAsMIRN200 microRNA, humanMitogen-Activated Protein Kinase 9Mitogen-Activated Protein Kinase KinasesNF-kappa BRela protein, mouseSTAT3 protein, humanSTAT3 Transcription FactorTranscription Factor RelATranscription Factors

Identifiers

PMID22364742
PMCPMC3319241
OpenAlexW1965334406

What OpenQuestion holds

Textmetadata
LicenceTDM
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.