Evidence map›Paper›PMID 34771470›Full record

ArticleCancers2021

The Pseudokinase TRIB3 Negatively Regulates the HER2 Receptor Pathway and Is a Biomarker of Good Prognosis in Luminal Breast Cancer.

Alba Orea-Soufi, Sonia Castillo-Lluva, Nélida Salvador-Tormo, Paola Martín-Cabrera, Silvia Recuero, Estíbaliz Gabicagogeascoa, Manuel Moreno-Valladares, Marina Mendiburu-Eliçabe, Adrián Blanco-Gómez, José Miguel Ramos-Pittol and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
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

17 authors at 7 institutions in 2 countries.

Alba Orea-SoufiDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.
Sonia Castillo-LluvaDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.ORCID 0000-0001-5357-7178
Nélida Salvador-TormoDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.
Paola Martín-CabreraDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.
Silvia RecueroDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.
Estíbaliz GabicagogeascoaDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.
Manuel Moreno-ValladaresOsakidetza Basque Health Service, Donostia University Hospital, 20014 San Sebastian, Spain.
Marina Mendiburu-EliçabeDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.ORCID 0000-0003-2573-8709
Adrián Blanco-GómezInstituto de Biología Molecular y Celular del Cáncer (IBMCC-CIC), Universidad de Salamanca/CSIC, 37007 Salamanca, Spain.ORCID 0000-0002-1956-088X
José Miguel Ramos-PittolInstitute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck 6020, Austria.ORCID 0000-0003-3753-5394
Elena García-TaboadaDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.
Alberto OcañaExperimental Therapeutics Unit, Hospital Clínico San Carlos (HCSC), Instituto de Investigaciones Sanitarias San Carlos (IdISSC), 28040 Madrid, Spain.ORCID 0000-0002-1067-9630
Francisco J CimasTranslational Research Unit, Translational Oncology Laboratory, Albacete University Hospital, Universidad de Castilla La Mancha (UCLM), 13071 Albacete, Spain.
Ander MatheuDepartment of Oncology, Biodonostia Health Research Institute, 20014 San Sebastián, Spain.
Isabel Álvarez-LópezOsakidetza Basque Health Service, Donostia University Hospital, 20014 San Sebastian, Spain.
Guillermo VelascoDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.ORCID 0000-0002-1994-2386
Mar LorenteDepartment of Biochemistry and Molecular Biology, School of Biology, Complutense University, 28040 Madrid, Spain.ORCID 0000-0003-0982-0956
Universidad Complutense de Madrid · ESBiogipuzkoa Health Research Institute · ESIkerbasque · ESInstituto de Investigación Sanitaria del Hospital Clínico San Carlos · ESUniversidad de Salamanca · ESUniversität Innsbruck · ATUniversity of Castilla-La Mancha · ES

Funding

Breast Cancer Now 2012NovSP033European Commission ITN-308 2016 721532Instituto de Salud Carlos III PI18/00442Ministry of Economy, Industry and Competitiveness RTI2018-094130-B-100
6 · The paper itself

Abstract

backgroundTribbles pseudokinase 3 (TRIB3) has been proposed to both promote and restrict cancer generation and progression. However, the precise mechanisms that determine this dual role of TRIB3 in cancer remain to be understood. In this study we aimed to investigate the role of TRIB3 in luminal breast cancer, the most frequent subtype of this malignancy.

methodsWe genetically manipulated TRIB3 expression in a panel of luminal breast cancer cell lines and analyzed its impact on cell proliferation, and the phosphorylation, levels, or subcellular localization of TRIB3 and other protein regulators of key signaling pathways in luminal breast cancer. We also analyzed TRIB3 protein expression in samples from luminal breast cancer patients and performed bioinformatic analyses in public datasets.

resultsTRIB3 enhanced the proliferation and AKT phosphorylation in luminal A (HER2-) but decreased them in luminal B (HER2+) breast cancer cell lines. TRIB3 negatively regulated the stability of HER2 in luminal B breast cancer cell lines. TRIB3 expression was associated with increased disease-free survival and a better response to therapy in luminal breast cancer patients.

conclusionsOur findings support the exploration of TRIB3 as a potential biomarker and therapeutic target in luminal breast cancer.

Indexed as

AKTcell signalingHER2Luminal breast cancertissue microarraysTRIB3

Identifiers

PMID34771470
PMCPMC8582533
OpenAlexW3208025119

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.