Evidence map›Paper›PMID 19966854›Full record

ArticleOncogene2010

The role of proto-oncogene Fra-1 in remodeling the tumor microenvironment in support of breast tumor cell invasion and progression.

Y P Luo, H Zhou, J Krueger, C Kaplan, D Liao, D Markowitz, C Liu, T Chen, T-H Chuang, R Xiang and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

55 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. FRA-1 as a Regulator of EMT and Metastasis in Breast Cancer.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Transcriptome Reprogramming of CD11bFrontiers in cell and developmental biology · 2020
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

11 authors at 2 institutions in 2 countries.

Y P LuoDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037, USA. ypluo@scripps.edu
H Zhou
J Krueger
C Kaplan
D Liao
D Markowitz
C Liu
T Chen
T-H Chuang
R Xiang
R A Reisfeld
Scripps Research Institute · USChongqing Medical University · CN

Funding

Cysteine Protease Network in Tumor Progression and TherapyR01CA127535 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI BACCALA, ROBERTO G · 2007 to 2011
$1.8M
Fra-1: A new target for a genomic breast cancer vaccineR01CA115751 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI REISFELD, RALPH A. · 2006 to 2009
$1.3M
NCI NIH HHS CA 115751NCI NIH HHS R01 CA115751NCI NIH HHS R01 CA127535
6 · The paper itself

Abstract

A growing body of evidence indicates that interactions between neoplastic cells and tumor-associated macrophages (TAMs) in the tumor microenvironment (TME) are crucial in promoting tumor cell invasion and progression. Macrophages have an ambiguous role in these processes as this M1 phenotype correlates with tumoricidal capacity, whereas TAMs of M2 phenotype exert tumor-promoting effects. In this study, we provide evidence that interactions between mouse breast tumor cells and TAMs remodel the TME, leading to the upregulation of Fra-1, a member of the FOS family of transcription factor. In turn, this proto-oncogene initiates activation of the IL-6/JAK/Stat3 signaling pathway. This creates a malignant switch in breast tumor cells, leading to increased release of proangiogenic factors MMP-9, vascular endothelial growth factor and transforming growth factor-beta from tumor cells and intensified invasion and progression of breast cancer. Proof of the concept for the crucial role played by transcription factor Fra-1 in regulating these processes was established by specific knockdown of Fra-1 with small interfering RNA, which resulted in a marked suppression of tumor cell invasion, angiogenesis and metastasis in a mouse breast cancer model. Such a strategy could eventually lead to future efficacious treatments of metastatic breast cancer.

Indexed as

AnimalsBlotting, WesternBreast NeoplasmsCell CommunicationCell SeparationDisease ProgressionFemaleFlow CytometryFluorescent Antibody TechniqueFos-Related Antigen 1MacrophagesMiceNeoplasm InvasivenessNeovascularization, PathologicProto-Oncogene Proteins c-fosReverse Transcriptase Polymerase Chain ReactionFos-Related Antigen 1Proto-Oncogene Proteins c-fosRNA, Small Interfering

Identifiers

PMID19966854
PMCPMC3032566
OpenAlexW1990435106

What OpenQuestion holds

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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.