Evidence map›Paper›PMID 25352952›Full record

ArticleGenes & cancer2014

miR-155 induced transcriptome changes in the MCF-7 breast cancer cell line leads to enhanced mitogen activated protein kinase signaling.

Elizabeth C Martin, Adrienne E Krebs, Hope E Burks, Steven Elliott, Melody Baddoo, Bridgette M Collins-Burow, Erik K Flemington, Matthew E Burow

Abstract read
In one paragraph

Article in Genes & cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. miR-155: An Important Role in Inflammation Response.Journal of immunology research · 2022
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Role of miR-155 in drug resistance of breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    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

8 authors.

Elizabeth C MartinDepartment of Medicine-Section of Hematology and Medical Oncology, Tulane University, New Orleans, LA.
Adrienne E KrebsDepartment of Medicine-Section of Hematology and Medical Oncology, Tulane University, New Orleans, LA.
Hope E BurksDepartment of Medicine-Section of Hematology and Medical Oncology, Tulane University, New Orleans, LA.
Steven ElliottDepartment of Medicine-Section of Hematology and Medical Oncology, Tulane University, New Orleans, LA.
Melody BaddooTulane Cancer Center, Tulane University, New Orleans, LA ; Department of Pathology, Tulane University, New Orleans, LA.
Bridgette M Collins-BurowDepartment of Medicine-Section of Hematology and Medical Oncology, Tulane University, New Orleans, LA.
Erik K FlemingtonTulane Cancer Center, Tulane University, New Orleans, LA ; Department of Pathology, Tulane University, New Orleans, LA.
Matthew E BurowDepartment of Medicine-Section of Hematology and Medical Oncology, Tulane University, New Orleans, LA ; Tulane Cancer Center, Tulane University, New Orleans, LA ; Department of Pharmacology, Tulane University, New Orleans, LA.

Funding

UNCOVERING THE MECHANISMS OF OSTEOSARCOMA METASTASIS SUPPRESSION BY MTBPP20RR020152 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI FORTGANG, ILANA · 2004 to 2011
$17.0M
Mentoring a Cancer Genetics ProgramP20GM103518 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI DEININGER, PRESCOTT L. · 2012 to 2013
$4.3M
Epstein Barr virus antisense transcriptionR01AI106676 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI FLEMINGTON, ERIK K · 2014 to 2018
$1.9M
Intercellular communication in Epstein Barr virus reactivationR01AI101046 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI FLEMINGTON, ERIK K · 2012 to 2016
$1.9M
Role of the cellular microRNA, miR-155, in EBV type III latency signalingR01CA138268 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI FLEMINGTON, ERIK K · 2009 to 2013
$1.5M
MEK5-Erk5 in breast cancer resistanceR01CA125806 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI BUROW, MATTHEW E. · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA125806NCI NIH HHS R01 CA138268NCRR NIH HHS P20 RR020152NIAID NIH HHS R01 AI101046NIAID NIH HHS R01 AI106676NIGMS NIH HHS P20 GM103518
6 · The paper itself

Abstract

A single microRNA (miRNA) has the potential to regulate thousands of genes and thus govern multiple signaling pathways at once. miR-155 is an oncogenic miRNA which regulates many cellular pathways, designating it as a multifaceted regulator of proliferation, chemo-resistance, and apoptosis. While many singular targeted effects of miR-155 have been defined and an oncogenic role has been attributed to miR-155 expression, the global effect of miR-155 on the cellular transcriptomes of an ER(+) breast cancer cell line has yet to be determined. Here we demonstrate that miR-155 expression increases tumorigenesis in vivo and we determine miR-155 mediated transcriptome changes through next generation sequencing analysis. miR-155 expression alters many signaling pathways, with the chief altered pathway being the MAPK signaling cascade and miR-155 induces shortening of target mRNA 3'UTRs and alternative isoform expression of MAPK related genes. In addition there is an observed increase in protein phosphorylation of components of MAPK signaling including ERK1/2 and AP-1 complex members (Fra-1 and c-Fos) as well as elevated gene expression of MAPK regulated genes Zeb1, Snail, Plaur, and SerpinE1.

Indexed as

3′UTRbreast cancerMAPKmicroRNA-155p38RNA-seq

Identifiers

PMID25352952
PMCPMC4209600

What OpenQuestion holds

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LicenceCC BY
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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.