Evidence map›Paper›PMID 23479725›Full record

ArticleThe Journal of biological chemistry2013

MicroRNA-584 and the protein phosphatase and actin regulator 1 (PHACTR1), a new signaling route through which transforming growth factor-β Mediates the migration and actin dynamics of breast cancer cells.

Nadège Fils-Aimé, Meiou Dai, Jimin Guo, Mayada El-Mousawi, Bora Kahramangil, Jean-Charles Neel, Jean-Jacques Lebrun

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.9field-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

41 citing papers in PubMed, 77 citations in OpenAlex.

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  5. Insight into the Role of the miR-584 Family in Human Cancers.International journal of molecular sciences · 2024
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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

7 authors at 2 institutions in 1 country.

Nadège Fils-AiméDivision of Medical Oncology, Department of Medicine, McGill University Health Center, Royal Victoria Hospital, Montreal, Quebec H3A 1A1, Canada.
Meiou Dai
Jimin Guo
Mayada El-Mousawi
Bora Kahramangil
Jean-Charles Neel
Jean-Jacques Lebrun
McGill University · CARoyal Victoria Hospital · CA

Funding

Canadian Institutes of Health Research MOP-114904
6 · The paper itself

Abstract

TGF-β plays an important role in breast cancer progression as a prometastatic factor, notably through enhancement of cell migration. It is becoming clear that microRNAs, a new class of small regulatory molecules, also play crucial roles in mediating tumor formation and progression. We found TGF-β to down-regulate the expression of the microRNA miR-584 in breast cancer cells. Furthermore, we identified PHACTR1, an actin-binding protein, to be positively regulated by TGF-β in a miR-584-dependent manner. Moreover, we found TGF-β-mediated down-regulation of miR-584 and increased expression of PHACTR1 to be required for TGF-β-induced cell migration of breast cancer cells. Indeed, both overexpression of miR-584 and knockdown of PHACTR1 resulted in a drastic reorganization of the actin cytoskeleton and reduced TGF-β-induced cell migration. Our data highlight a novel signaling route whereby TGF-β silences the expression of miR-584, resulting in enhanced PHACTR1 expression, and further leading to actin rearrangement and breast cancer cell migration.

Indexed as

Cell MovementActinsBreast NeoplasmsCell Line, TumorCytoskeletonFemaleGene Expression Regulation, NeoplasticGene SilencingHumansMicrofilament ProteinsMicroRNAsNeoplasm ProteinsRNA, NeoplasmSignal TransductionTransforming Growth Factor betaActinsMicrofilament ProteinsMicroRNAsMIRN584 microRNA, humanNeoplasm ProteinsPHACTR1 protein, humanRNA, NeoplasmTransforming Growth Factor beta

Identifiers

PMID23479725
PMCPMC3636869
OpenAlexW2046855348

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.