Evidence map›Paper›PMID 23844004›Full record

ArticlePloS one2013

Exosome-bound WD repeat protein Monad inhibits breast cancer cell invasion by degrading amphiregulin mRNA.

Makio Saeki, Hiroshi Egusa, Yuya Kamano, Yoshito Kakihara, Walid A Houry, Hirofumi Yatani, Shinzaburo Noguchi, Yoshinori Kamisaki

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Makio SaekiDepartment of Pharmacology, Graduate School of Dentistry, Osaka University, Suita, Osaka, Japan. msaeki@dent.osaka-u.ac.jp
Hiroshi Egusa
Yuya Kamano
Yoshito Kakihara
Walid A Houry
Hirofumi Yatani
Shinzaburo Noguchi
Yoshinori Kamisaki
Osaka University · JPUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased stabilization of mRNA coding for key cancer genes can contribute to invasiveness. This is achieved by down-regulation of exosome cofactors, which bind to 3'-UTR in cancer-related genes. Here, we identified amphiregulin, an EGFR ligand, as a target of WD repeat protein Monad, a component of R2TP/prefoldin-like complex, in MDA-MB-231 breast cancer cells. Monad specifically interacted with both the 3'-UTR of amphiregulin mRNA and the RNA degrading exosome, and enhanced decay of amphiregulin transcripts. Knockdown of Monad increased invasion and this effect was abolished with anti-amphiregulin neutralizing antibody. These results suggest that Monad could prevent amphiregulin-mediated invasion by degrading amphiregulin mRNA.

Indexed as

RNA StabilityAmphiregulinApoptosis Regulatory ProteinsAutocrine CommunicationBreast NeoplasmsCarrier ProteinsCell Line, TumorCell ProliferationEGF Family of ProteinsExosomesFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGlycoproteinsHumansIntercellular Signaling Peptides and ProteinsAmphiregulinApoptosis Regulatory ProteinsAREG protein, humanCarrier ProteinsDNAAF10 protein, humanEGF Family of ProteinsGlycoproteinsIntercellular Signaling Peptides and ProteinsRNA, MessengerRPAP3 protein, human

Identifiers

PMID23844004
PMCPMC3701000
OpenAlexW2040885247

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.