Evidence map›Paper›PMID 26865667›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2016

Dose- and Time-Dependent Transcriptional Response of Ishikawa Cells Exposed to Genistein.

Jorge M Naciff, Zubin S Khambatta, Gregory J Carr, Jay P Tiesman, David W Singleton, Sohaib A Khan, George P Daston

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-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

6 citing papers in PubMed, 15 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

7 authors at 2 institutions in 1 country.

Jorge M Naciff*Mason Business Center, The Procter and Gamble Company, Mason, Ohio 45040 naciff.jm@pg.com.
Zubin S Khambatta*Mason Business Center, The Procter and Gamble Company, Mason, Ohio 45040.
Gregory J Carr*Mason Business Center, The Procter and Gamble Company, Mason, Ohio 45040.
Jay P Tiesman*Mason Business Center, The Procter and Gamble Company, Mason, Ohio 45040.
David W SingletonDepartment of Cell Biology, Neurobiology, and Anatomy, Vontz Center for Molecular Studies, University of Cincinnati, Cincinnati, Ohio 45267.
Sohaib A KhanDepartment of Cell Biology, Neurobiology, and Anatomy, Vontz Center for Molecular Studies, University of Cincinnati, Cincinnati, Ohio 45267.
George P Daston*Mason Business Center, The Procter and Gamble Company, Mason, Ohio 45040.
Procter & Gamble (United States) · USUniversity of Cincinnati · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To further define the utility of the Ishikawa cells as a reliable in vitro model to determine the potential estrogenic activity of chemicals of interest, transcriptional changes induced by genistein (GES) in Ishikawa cells at various doses (10 pM, 1 nM, 100 nM, and 10 μM) and time points (8, 24, and 48 h) were identified using a comprehensive microarray approach. Trend analysis indicated that the expression of 5342 unique genes was modified by GES in a dose- and time-dependent manner (P ≤ 0.0001). However, the majority of gene expression changes induced in Ishikawa cells were elicited by the highest dose of GES evaluated (10 μM). The GES' estrogenic activity was identified by comparing the Ishikawa cells' response to GES versus 17 α-ethynyl estradiol (EE, at equipotent doses, ie, 10 μM vs 1 μM, respectively) and was defined by changes in the expression of 284 unique genes elicited by GES and EE in the same direction, although the magnitude of the change for some genes was different. Further, comparing the response of the Ishikawa cells exposed to high doses of GES and EE versus the response of the juvenile rat uterus exposed to EE, we identified 66 unique genes which were up- or down regulated in a similar manner in vivo as well as in vitro Genistein elicits changes in multiple molecular pathways affecting various biological processes particularly associated with cell organization and biogenesis, regulation of translation, cell proliferation, and intracellular transport; processes also affected by estrogen exposure in the uterus of the rat. These results indicate that Ishikawa cells are capable of generating a biologically relevant estrogenic response and offer an in vitro model to assess this mode of action.

Indexed as

AdenocarcinomaAnimalsCell Line, TumorDose-Response Relationship, DrugEndometrial NeoplasmsEstradiolFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGenisteinHumansOligonucleotide Array Sequence AnalysisPhytoestrogensRatsTranscription, GeneticUterusEstradiolGenisteinPhytoestrogensgene expression profilinggenisteinhuman uterus.in vitroIshikawa cellsmicroarrays

Identifiers

PMID26865667
PMCPMC4914796
OpenAlexW2309621810

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.