Evidence map›Paper›PMID 28924161›Full record

ArticleScientific reports2017

Molecular mechanisms involved in the non-monotonic effect of bisphenol-a on ca2+ entry in mouse pancreatic β-cells.

Sabrina Villar-Pazos, Juan Martinez-Pinna, Manuel Castellano-Muñoz, Paloma Alonso-Magdalena, Laura Marroqui, Ivan Quesada, Jan-Ake Gustafsson, Angel Nadal

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 89 citations in OpenAlex.

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  17. Endocrine disruptors in plastics alter β-cell physiology and increase the risk of diabetes mellitus.American journal of physiology. Endocrinology and metabolism · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 3 countries.

Sabrina Villar-PazosCIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM) and Institute of Bioenginering, Miguel Hernández University of Elche, Elche, Alicante, Spain.
Juan Martinez-PinnaDepartamento de Fisiología, Genética y Microbiología, Universidad de Alicante, Alicante, Spain.
Manuel Castellano-MuñozCIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM) and Institute of Bioenginering, Miguel Hernández University of Elche, Elche, Alicante, Spain.
Paloma Alonso-MagdalenaCIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM) and Institute of Bioenginering, Miguel Hernández University of Elche, Elche, Alicante, Spain.
Laura MarroquiCIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM) and Institute of Bioenginering, Miguel Hernández University of Elche, Elche, Alicante, Spain.
Ivan QuesadaCIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM) and Institute of Bioenginering, Miguel Hernández University of Elche, Elche, Alicante, Spain.
Jan-Ake GustafssonDepartment of Cell Biology and Biochemistry, Center for Nuclear Receptors and Cell Signaling, University of Houston, Houston, Texas, USA.
Angel NadalCIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM) and Institute of Bioenginering, Miguel Hernández University of Elche, Elche, Alicante, Spain. nadal@umh.es.ORCID 0000-0003-4178-2152
Universitat de Miguel Hernández d'Elx · ESKarolinska Institutet · SEUniversity of Alicante · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In regulatory toxicology, the dose-response relationship is a key element towards fulfilling safety assessments and satisfying regulatory authorities. Conventionally, the larger the dose, the greater the response, following the dogma "the dose makes the poison". Many endocrine disrupting chemicals, including bisphenol-A (BPA), induce non-monotonic dose response (NMDR) relationships, which are unconventional and have tremendous implications in risk assessment. Although several molecular mechanisms have been proposed to explain NMDR relationships, they are largely undemonstrated. Using mouse pancreatic β-cells from wild-type and oestrogen receptor ERβ-/- mice, we found that exposure to increasing doses of BPA affected Ca

Indexed as

AnimalsBenzhydryl CompoundsBisphenol A CompoundsCalciumCalcium Channels, R-TypeCalcium SignalingCation Transport ProteinsDose-Response Relationship, DrugEstrogen Receptor betaGene Expression RegulationInsulin-Secreting CellsMaleMiceMice, KnockoutPhenolsBenzhydryl Compoundsbisphenol ABisphenol A CompoundsCacna1e protein, mouseCalciumCalcium Channels, R-TypeCation Transport ProteinsEstrogen Receptor betaPhenols

Identifiers

PMID28924161
PMCPMC5603522
OpenAlexW2755182163

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.