Evidence map›Paper›PMID 28524356›Full record

ArticleJournal of applied toxicology : JAT2017

Association between YAP expression in neoplastic and non-neoplastic breast tissue with arsenic urinary levels.

Gladis Michel-Ramirez, Rogelio Recio-Vega, Guadalupe Ocampo-Gomez, Eduardo Palacios-Sanchez, Manuel Delgado-Macias, Manuel Delgado-Gaona, Robert Clark Lantz, Jay Gandolfi, Tania Gonzalez-Cortes

Open access · greenAbstract read
In one paragraph

Article in Journal of applied toxicology : JAT, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 3 institutions in 2 countries.

Gladis Michel-RamirezDepartment of Environmental Health, Biomedical Research Center, School of Medicine, University of Coahuila, Torreon, Coahuila, Mexico.
Rogelio Recio-VegaDepartment of Environmental Health, Biomedical Research Center, School of Medicine, University of Coahuila, Torreon, Coahuila, Mexico.ORCID http://orcid.org/0000-0002-5976-6516
Guadalupe Ocampo-GomezDepartment of Environmental Health, Biomedical Research Center, School of Medicine, University of Coahuila, Torreon, Coahuila, Mexico.
Eduardo Palacios-SanchezDepartment of Gynecologic Oncology, Mexican Institute of Social Security, Torreon, Coahuila, México.
Manuel Delgado-MaciasDepartment of Medical Education, School of Medicine, University of Coahuila, Torreon, Coahuila, México.
Manuel Delgado-GaonaDepartment of Pathology, University General Hospital, Torreon, Coahuila, Mexico.
Robert Clark LantzSouthwest Environmental Health Science Center, University of Arizona, Tucson, AZ, USA.
Jay GandolfiSouthwest Environmental Health Science Center, University of Arizona, Tucson, AZ, USA.
Tania Gonzalez-CortesDepartment of Environmental Health, Biomedical Research Center, School of Medicine, University of Coahuila, Torreon, Coahuila, Mexico.
Universidad Autónoma de Coahuila · MXUniversity of Arizona · USMexican Social Security Institute · MX

Funding

TRANSPORT OF TRACE METALS IN A POLLUTED AQUIFERP42ES004940 · NIEHS · UNIVERSITY OF ARIZONA · PI Jon D Chorover · 1990 to 2026
$68.1M
NIEHS NIH HHS P42 ES004940
6 · The paper itself

Abstract

The Hippo pathway regulates cell proliferation and apoptosis and it has been noted that loss of critical components of this pathway can lead to uncontrolled cell growth. Yes-associated protein (YAP) is an important component of this Hippo pathway because YAP is the nuclear effector of the Hippo tumor suppressor pathway and it is crucial for the response to oxidative stress induced by cellular process and by different xenobiotics, including arsenic. It has been proposed that YAP dysregulation can contribute to a malignant cellular phenotype acting as both a tumor suppressor and an oncogene. The aim of the study was to assess and compare the expression of YAP in neoplastic and non-neoplastic breast tissue of women chronically exposed to arsenic through drinking water. YAP expression was assessed by immunohistochemistry in 120 breast biopsies from women with breast cancer and from women with other non-neoplastic breast pathologies. Arsenic concentration was quantified in urine. The results disclosed a significant lower percentage of cytoplasm YAP expression in cases and that YAP high-intensity staining in the cytoplasm but not in the nucleus decreases the risk for breast cancer. In conclusion, our overall data suggest that YAP may act as a tumor suppressor protein because their reduced expression in cases, which can induce an environment favorable for inhibition of apoptosis and promoting cellular proliferation by increasing genetic instability of cells, which might contribute to the pathogenesis of cancer. Copyright © 2017 John Wiley & Sons, Ltd.

Indexed as

Adaptor Proteins, Signal TransducingAdultAnthropometryArsenicBreastBreast NeoplasmsCell Line, TumorCell NucleusCell ProliferationCross-Sectional StudiesCytoplasmFemaleHumansImmunohistochemistryLife StyleMiddle AgedAdaptor Proteins, Signal TransducingArsenicPhosphoproteinsTranscription FactorsTumor Suppressor ProteinsYAP1 protein, humanYAP-Signaling Proteinsarsenicbreast cancerYAPYes Associated Protein

Identifiers

PMID28524356
PMCPMC5790116
OpenAlexW2615417666

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.