Evidence map›Paper›PMID 26976638›Full record

ArticleMolecular and cellular biology2016

Chordin-Like 1 Suppresses Bone Morphogenetic Protein 4-Induced Breast Cancer Cell Migration and Invasion.

Chanèle Cyr-Depauw, Jason J Northey, Sébastien Tabariès, Matthew G Annis, Zhifeng Dong, Sean Cory, Michael Hallett, Jonathan P Rennhack, Eran R Andrechek, Peter M Siegel

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 72 citations in OpenAlex.

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  9. Expression profiling of luminal B breast tumor in Indian women.Journal of cancer research and clinical oncology · 2023
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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

10 authors at 3 institutions in 2 countries.

Chanèle Cyr-DepauwGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada Department of Biochemistry, McGill University, Montréal, Québec, Canada.
Jason J NortheyGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada Department of Biochemistry, McGill University, Montréal, Québec, Canada.
Sébastien TabarièsGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada Department of Medicine, McGill University, Montréal, Québec, Canada.
Matthew G AnnisGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada Department of Medicine, McGill University, Montréal, Québec, Canada.
Zhifeng DongGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada Department of Medicine, McGill University, Montréal, Québec, Canada.
Sean CoryMcGill Centre for Bioinformatics, Montréal, Québec, Canada.
Michael HallettMcGill Centre for Bioinformatics, Montréal, Québec, Canada.
Jonathan P RennhackDepartment of Physiology, Michigan State University, East Lansing, Michigan, USA.
Eran R AndrechekDepartment of Physiology, Michigan State University, East Lansing, Michigan, USA.
Peter M SiegelGoodman Cancer Research Centre, McGill University, Montréal, Québec, Canada Department of Biochemistry, McGill University, Montréal, Québec, Canada Department of Medicine, McGill University, Montréal, Québec, Canada peter.siegel@mcgill.ca.
McGill University Health Centre · CAMichigan State University · USMcGill University · CA

Funding

The Role of E2F2 in HER2 Positive Breast CancerF99CA212221 · NCI · MICHIGAN STATE UNIVERSITY · PI RENNHACK, JONATHAN · 2016 to 2017
$85k
6 · The paper itself

Abstract

ShcA is an important mediator of ErbB2- and transforming growth factor β (TGF-β)-induced breast cancer cell migration, invasion, and metastasis. We show that in the context of reduced ShcA levels, the bone morphogenetic protein (BMP) antagonist chordin-like 1 (Chrdl1) is upregulated in numerous breast cancer cells following TGF-β stimulation. BMPs have emerged as important modulators of breast cancer aggressiveness, and we have investigated the ability of Chrdl1 to block BMP-induced increases in breast cancer cell migration and invasion. Breast cancer-derived conditioned medium containing elevated concentrations of endogenous Chrdl1, as well as medium containing recombinant Chrdl1, suppresses BMP4-induced signaling in multiple breast cancer cell lines. Live-cell migration assays reveal that BMP4 induces breast cancer migration, which is effectively blocked by Chrdl1. We demonstrate that BMP4 also stimulated breast cancer cell invasion and matrix degradation, in part, through enhanced metalloproteinase 2 (MMP2) and MMP9 activity that is antagonized by Chrdl1. Finally, high Chrdl1 expression was associated with better clinical outcomes in patients with breast cancer. Together, our data reveal that Chrdl1 acts as a negative regulator of malignant breast cancer phenotypes through inhibition of BMP signaling.

Indexed as

Bone Morphogenetic Protein 4Breast NeoplasmsCell Line, TumorCell MovementCulture Media, ConditionedEye ProteinsFemaleGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessNerve Tissue ProteinsPrognosisTransforming Growth Factor betaUp-RegulationBMP4 protein, humanBone Morphogenetic Protein 4CHRDL1 protein, humanCulture Media, ConditionedEye ProteinsNerve Tissue ProteinsTransforming Growth Factor beta

Identifiers

PMID26976638
PMCPMC4859683
OpenAlexW2345509148

What OpenQuestion holds

Textmetadata
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.