Evidence map›Paper›PMID 26552463›Full record

ArticleThe Korean journal of internal medicine2015

The effects of nonyl phenoxypolyethoxyl ethanol on cell damage pathway gene expression in SK-NSH cells.

Samel Park, Il-woong Hwang, Jin-sheon Kim, Hyo-chul Kang, Su-Yeon Park, Hyo-wook Gil, Ho-yeon Song, Sae-yong Hong

Open access · goldAbstract readCase Reports
In one paragraph

Article in The Korean journal of internal medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

8 authors at 1 institution in 1 country.

Samel ParkDepartment of Internal Medicine, Soonchunhyang University College of Medicine, Cheonan, Korea.
Il-woong HwangPesticide Intoxication Institute, Soonchunhyang University College of Medicine, Cheonan, Korea.
Jin-sheon KimPesticide Intoxication Institute, Soonchunhyang University College of Medicine, Cheonan, Korea.
Hyo-chul KangDepartment of Internal Medicine, Soonchunhyang University College of Medicine, Cheonan, Korea.
Su-Yeon ParkBiostatistical Consulting Unit, Soonchunhyang University College of Medicine, Cheonan, Korea.
Hyo-wook GilDepartment of Internal Medicine, Soonchunhyang University College of Medicine, Cheonan, Korea.
Ho-yeon SongDepartment of Microbiology, Soonchunhyang University College of Medicine, Cheonan, Korea.
Sae-yong HongDepartment of Internal Medicine, Soonchunhyang University College of Medicine, Cheonan, Korea.
Soonchunhyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsMost pesticide formulations contain both chief and additive ingredients. But, the additives may not have been tested as thoroughly as the chief ingredients. The surfactant, nonyl phenoxypolyethoxylethanol (NP40), is an additive frequently present in pesticide formulations. We investigated the effects of NP40 and other constituents of a validamycin pesticide formulation on cell viability and on the expression of genes involved in cell damage pathways.

methodsThe effects of validamycin pesticide ingredients on cell viability and of NP40 on the mRNA expression of 80 genes involved in nine key cellular pathways were examined in the human neuroblastoma SK-N-SH cell line.

resultsThe chemicals present in the validamycin pesticide formulation were cytotoxic to SK-N-SH cells and NP40 showed the greatest cytotoxicity. A range of gene expression changes were identified, with both up- and down-regulation of genes within the same pathway. However, all genes tested in the necrosis signaling pathway were down-regulated and all genes tested in the cell cycle checkpoint/arrest pathway were up-regulated. The median fold-change in gene expression was significantly higher in the cell cycle checkpoint/arrest pathway than in the hypoxia pathway category (p = 0.0064). The 70 kDa heat shock protein 4 gene, within the heat shock protein/unfolded protein response category, showed the highest individual increase in expression (26.1-fold).

conclusionsNP40 appeared to be particularly harmful, inducing gene expression changes that indicated genotoxicity, activation of the cell death (necrosis signaling) pathway, and induction of the 70 kDa heat shock protein 4 gene.

Indexed as

AgedCell Cycle CheckpointsCell Line, TumorCell SurvivalDose-Response Relationship, DrugFemaleGene Expression RegulationGenes, cdcHSP110 Heat-Shock ProteinsHumansInositolNecrosisNeuronsNonoxynolPesticidesRNA, MessengerHSP110 Heat-Shock ProteinsHSPA4 protein, humanInositolNonoxynolPesticidesRNA, MessengerSurface-Active AgentsvalidamycinsCell damage pathwaysGene expressionNonyl phenoxypolyethoxylethanolSurface-active agentsValidamycins

Identifiers

PMID26552463
PMCPMC4642017
OpenAlexW2198304039

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.