Evidence map›Paper›PMID 21190936›Full record

ArticleThe Journal of biological chemistry2011

Extracellular signal-regulated kinase 8 (ERK8) controls estrogen-related receptor α (ERRα) cellular localization and inhibits its transcriptional activity.

Matteo Rossi, David Colecchia, Carlo Iavarone, Angela Strambi, Federica Piccioni, Arturo Verrotti di Pianella, Mario Chiariello

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Atypical MAPKs in cancer.The FEBS journal · 2025
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  15. The Atypical MAP Kinase SWIP-13/ERK8 Regulates Dopamine Transporters through a Rho-Dependent Mechanism.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  16. Article
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  18. The estrogen-related receptors (ERRs): potential targets against bone loss.Cellular and molecular life sciences : CMLS · 2016
    Review
  19. 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

7 authors at 4 institutions in 1 country.

Matteo RossiFrom the Istituto Toscano Tumori-Core Research Laboratory, Signal Transduction Unit, Siena,; the Università degli Studi di Siena, and.
David ColecchiaFrom the Istituto Toscano Tumori-Core Research Laboratory, Signal Transduction Unit, Siena,; the Università degli Studi di Siena, and.
Carlo IavaroneIstituto di Endocrinologia e Oncologia Sperimentale, CNR, Napoli.
Angela StrambiFrom the Istituto Toscano Tumori-Core Research Laboratory, Signal Transduction Unit, Siena.
Federica Piccionithe CEINGE-Biotecnologie Avanzate, Napoli.
Arturo Verrotti di Pianellathe CEINGE-Biotecnologie Avanzate, Napoli,; the Dipartimento di Biochimica e Biotecnologie Mediche, Università degli Studi di Napoli, Napoli, and.
Mario ChiarielloFrom the Istituto Toscano Tumori-Core Research Laboratory, Signal Transduction Unit, Siena,; Istituto di Endocrinologia e Oncologia Sperimentale, CNR, Napoli,; the Istituto di Fisiologia Clinica, Sede di Siena, CNR, Siena, Italy. Electronic address: mario.chiariello@ittumori.it.
Ceinge Biotecnologie Avanzate (Italy) · ITInstitute for Experimental Endocrinology and Oncology · ITUniversity of Siena · ITToscana Life Sciences · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ERK8 (MAPK15) is a large MAP kinase already implicated in the regulation of the functions of different nuclear receptors and in cellular proliferation and transformation. Here, we identify ERRα as a novel ERK8-interacting protein. As a consequence of such interaction, ERK8 induces CRM1-dependent translocation of ERRα to the cytoplasm and inhibits its transcriptional activity. Also, we identify in ERK8 two LXXLL motifs, typical of agonist-bound nuclear receptor corepressors, as necessary features for this MAP kinase to interact with ERRα and to regulate its cellular localization and transcriptional activity. Ultimately, we demonstrate that ERK8 is able to counteract, in immortalized human mammary cells, ERRα activation induced by the EGF receptor pathway, often deregulated in breast cancer. Altogether, these results reveal a novel function for ERK8 as a bona fide ERRα corepressor, involved in control of its cellular localization by nuclear exclusion, and suggest a key role for this MAP kinase in the regulation of the biological activities of this nuclear receptor.

Indexed as

Active Transport, Cell NucleusAmino Acid MotifsAnimalsCell NucleusERRalpha Estrogen-Related ReceptorExportin 1 ProteinExtracellular Signal-Regulated MAP KinasesHEK293 CellsHeLa CellsHumansKaryopherinsMiceReceptors, Cytoplasmic and NuclearReceptors, EstrogenTranscription, GeneticERRalpha Estrogen-Related ReceptorExportin 1 ProteinExtracellular Signal-Regulated MAP KinasesKaryopherinsMAPK15 protein, humanReceptors, Cytoplasmic and NuclearReceptors, Estrogen

Identifiers

PMID21190936
PMCPMC3048734
OpenAlexW1973189169

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.