Evidence map›Paper›PMID 29249802›Full record

ArticleOncogene2018

A CREB3-regulated ER-Golgi trafficking signature promotes metastatic progression in breast cancer.

Breege V Howley, Laura A Link, Simon Grelet, Maya El-Sabban, Philip H Howe

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

51 citing papers in PubMed, 70 citations in OpenAlex.

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  16. Membrane trafficking alterations in breast cancer progression.Frontiers in cell and developmental biology · 2024
    Review
  17. Review
  18. Review
  19. Article
  20. USO1 expression is dysregulated in non-small cell lung cancer.Translational lung cancer research · 2022
    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

5 authors at 2 institutions in 1 country.

Breege V HowleyDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.
Laura A LinkDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.
Simon GreletDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.
Maya El-SabbanDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.
Philip H HoweDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA. howep@musc.edu.ORCID 0000-0002-1358-1313
Medical University of South Carolina · USKent State University · US

Funding

South Carolina IDeA Networks of Biomedical Research (SC INBRE V)P20GM103499 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI EDIE C GOLDSMITH · 2012 to 2026
$61.0M
Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
SC COBRE for Developmentally Based Cardiovascular DiseasesP30GM103342 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KERN, MICHAEL J · 2012 to 2016
$5.5M
Pilot and Feasibility Project ProgramP30GM103331 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KIRKWOOD, KEITH L · 2012 to 2016
$5.2M
TGF-regulated EMTR01CA154663 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Philip H Howe · 2011 to 2026
$5.1M
TRANSFORMING GROWTH FACTOR BETA SIGNALING PATHWAYSR01CA055536 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HOWE, PHILIP H · 1997 to 2017
$5.0M
NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA055536NCI NIH HHS R01 CA154663NIGMS NIH HHS P20 GM103499NIGMS NIH HHS P30 GM103331NIGMS NIH HHS P30 GM103342
6 · The paper itself

Abstract

In order to better understand the process of breast cancer metastasis, we have generated a mammary epithelial progression series of increasingly aggressive cell lines that metastasize to lung. Here we demonstrate that upregulation of an endoplasmic reticulum (ER) to Golgi trafficking gene signature in metastatic cells enhances transport kinetics, which promotes malignant progression. We observe increased ER-Golgi trafficking, an altered secretome and sensitivity to the retrograde transport inhibitor brefeldin A (BFA) in cells that metastasize to lung. CREB3 was identified as a transcriptional regulator of upregulated ER-Golgi trafficking genes ARF4, COPB1, and USO1, and silencing of these genes attenuated the metastatic phenotype in vitro and lung colonization in vivo. Furthermore, high trafficking gene expression significantly correlated with increased risk of distant metastasis and reduced relapse-free and overall survival in breast cancer patients, suggesting that modulation of ER-Golgi trafficking plays an important role in metastatic progression.

Indexed as

AnimalsBreast NeoplasmsCyclic AMP Response Element-Binding ProteinDisease ProgressionEndoplasmic ReticulumFemaleGene Expression Regulation, NeoplasticGolgi ApparatusHEK293 CellsHumansMCF-7 CellsMiceMice, Inbred NODMice, SCIDMice, TransgenicMicroarray AnalysisCREB3 protein, humanCyclic AMP Response Element-Binding Protein

Identifiers

PMID29249802
PMCPMC5844805
OpenAlexW2774649052

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.