Evidence map›Paper›PMID 27941878›Full record

ArticleOncogene2017

The molecular mechanisms underlying the ERα-36-mediated signaling in breast cancer.

S Omarjee, J Jacquemetton, C Poulard, N Rochel, A Dejaegere, Y Chebaro, I Treilleux, E Marangoni, L Corbo, M Le Romancer

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  10. Estrogen Receptors-Mediated Apoptosis in Hormone-Dependent Cancers.International journal of molecular sciences · 2022
    Review
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  16. The Role of ERα36 in Development and Tumor Malignancy.International journal of molecular sciences · 2020
    Review
  17. Review
  18. Article
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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 7 institutions in 2 countries.

S OmarjeeUniversité Lyon 1, Lyon, France.
J JacquemettonUniversité Lyon 1, Lyon, France.
C PoulardUniversité Lyon 1, Lyon, France.
N RochelInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
A DejaegereInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Y ChebaroInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
I TreilleuxUniversité Lyon 1, Lyon, France.
E MarangoniInstitut Curie, Translational Research Department, Paris, France.
L CorboUniversité Lyon 1, Lyon, France.
M Le RomancerUniversité Lyon 1, Lyon, France.
Centre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Strasbourg · FRCentre de Recherche en Cancérologie de Lyon · FRCentre Léon Bérard · FRInserm · FRInstitut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alterations in estrogen-mediated cellular signaling have largely been implicated in the pathogenesis of breast cancer. Here, we investigated the signaling regulation of a splice variant of the estrogen receptor, namely estrogen receptor (ERα-36), associated with a poor prognosis in breast cancers. Coupling in vitro and in vivo approaches we determined the precise sequential molecular events of a new estrogen signaling network in an ERα-negative cell line and in an original patient-derived xenograft. After estrogen treatment, ERα-36 rapidly associates with Src at the level of the plasma membrane, initiating downstream cascades, including MEK1/ERK activation and paxillin phosphorylation on S126, which in turn triggers a higher expression of cyclin D1. Of note, the direct binding of ERα-36 to ERK2 prevents its dephosphorylation by MKP3 and enhances the downstream signaling. These findings improve our understanding of the regulation of non-genomic estrogen signaling and open new avenues for personalized therapeutic approaches targeting Src or MEK in ERα-36-positive patients.

Indexed as

AnimalsBreast NeoplasmsEstrogen Receptor alphaFemaleHumansMAP Kinase Kinase 1MCF-7 CellsMiceOncogene Protein pp60(v-src)Protein IsoformsSignal TransductionXenograft Model Antitumor AssaysESR1 protein, humanEstrogen Receptor alphaMAP2K1 protein, humanMAP Kinase Kinase 1Oncogene Protein pp60(v-src)Protein Isoforms

Identifiers

PMID27941878
PMCPMC5422711
OpenAlexW2565361814

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.