Evidence map›Paper›PMID 25226522›Full record

ArticlePloS one2014

Endoplasmic reticulum stress induces different molecular structural alterations in human dilated and ischemic cardiomyopathy.

Ana Ortega, Esther Roselló-Lletí, Estefanía Tarazón, Maria Micaela Molina-Navarro, Luis Martínez-Dolz, José Ramón González-Juanatey, Francisca Lago, Jose David Montoro-Mateos, Antonio Salvador, Miguel Rivera and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

48 citing papers in PubMed, 77 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

11 authors at 1 institution in 1 country.

Ana OrtegaCardiocirculatory Unit, Health Research Institute of La Fe University Hospital, Valencia, Spain.
Esther Roselló-LletíCardiocirculatory Unit, Health Research Institute of La Fe University Hospital, Valencia, Spain.
Estefanía TarazónCardiocirculatory Unit, Health Research Institute of La Fe University Hospital, Valencia, Spain.
Maria Micaela Molina-NavarroCardiocirculatory Unit, Health Research Institute of La Fe University Hospital, Valencia, Spain.
Luis Martínez-DolzHeart Failure and Transplantation Unit, Cardiology Department, La Fe University Hospital, Valencia, Spain.
José Ramón González-JuanateyCellular and Molecular Cardiology Research Unit, Department of Cardiology and Institute of Biomedical Research, University Clinical Hospital, Santiago de Compostela, Spain.
Francisca LagoCellular and Molecular Cardiology Research Unit, Department of Cardiology and Institute of Biomedical Research, University Clinical Hospital, Santiago de Compostela, Spain.
Jose David Montoro-MateosCardiocirculatory Unit, Health Research Institute of La Fe University Hospital, Valencia, Spain.
Antonio SalvadorHeart Failure and Transplantation Unit, Cardiology Department, La Fe University Hospital, Valencia, Spain.
Miguel RiveraCardiocirculatory Unit, Health Research Institute of La Fe University Hospital, Valencia, Spain.
Manuel PortolésCardiocirculatory Unit, Health Research Institute of La Fe University Hospital, Valencia, Spain.
Hospital Universitari i Politècnic La Fe · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe endoplasmic reticulum (ER) is a multifunctional organelle responsible for the synthesis and folding of proteins as well as for signalling and calcium storage, that has been linked to the contraction-relaxation process. Perturbations of its homeostasis activate a stress response in diseases such as heart failure (HF). To elucidate the alterations in ER molecular components, we analyze the levels of ER stress and structure proteins in human dilated (DCM) and ischemic (ICM) cardiomyopathies, and its relationship with patient's functional status. METHODS AND

resultsWe examined 52 explanted human hearts from DCM (n = 21) and ICM (n = 21) subjects and 10 non-failing hearts as controls. Our results showed specific changes in stress (IRE1, p<0.05; p-IRE1, p<0.05) and structural (Reticulon 1, p<0.01) protein levels. The stress proteins GRP78, XBP1 and ATF6 as well as the structural proteins RRBP1, kinectin, and Nogo A and B, were upregulated in both DCM and ICM patients. Immunofluorescence results were concordant with quantified Western blot levels. Moreover, we show a novel relationship between stress and structural proteins. RRBP1, involved in procollagen synthesis and remodeling, was related with left ventricular function.

conclusionsIn the present study, we report the existence of alterations in ER stress response and shaping proteins. We show a plausible effect of the ER stress on ER structure in a suitable sample of DCM and ICM subjects. Patients with higher values of RRBP1 had worse left ventricular function.

Indexed as

Endoplasmic Reticulum StressAdultCardiomyopathy, DilatedEndoplasmic ReticulumEndoplasmic Reticulum Chaperone BiPFemaleHeart VentriclesHumansMaleMiddle AgedMyocardial IschemiaProtein TransportProteomeEndoplasmic Reticulum Chaperone BiPHSPA5 protein, humanProteome

Identifiers

PMID25226522
PMCPMC4166610
OpenAlexW2014301106

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Registered trials

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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.