Evidence map›Paper›PMID 31020328›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2019

A Novel Open Access Web Portal for Integrating Mechanistic and Toxicogenomic Study Results.

Jeffrey J Sutherland, James L Stevens, Kamin Johnson, Navin Elango, Yue W Webster, Bradley J Mills, Daniel H Robertson

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. A Set of Six Gene Expression Biomarkers Identify Rat Liver Tumorigens in Short-term Assays.Toxicological sciences : an official journal of the Society of Toxicology · 2020
    Article
  4. Article
  5. Assessing Chemical-Induced Liver InjuryFrontiers in genetics · 2019
    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

7 authors at 4 institutions in 1 country.

Jeffrey J SutherlandIndiana Biosciences Research Institute, 1345 W. 16th St. Suite 300, Indianapolis, IN 46202.
James L StevensEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285.
Kamin JohnsonCorteva AgriscienceTM, Agriculture Division of DowDuPontTM, 9330 Zionsville Rd, Indianapolis, Indiana, 46268.
Navin ElangoCorteva AgriscienceTM, Agriculture Division of DowDuPontTM, 9330 Zionsville Rd, Indianapolis, Indiana, 46268.
Yue W WebsterEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285.
Bradley J MillsIndiana Biosciences Research Institute, 1345 W. 16th St. Suite 300, Indianapolis, IN 46202.
Daniel H RobertsonIndiana Biosciences Research Institute, 1345 W. 16th St. Suite 300, Indianapolis, IN 46202.
Indiana Biosciences Research Institute · USCorteva (United States) · USEli Lilly (United States) · USGreenWood Resources (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Applying toxicogenomics to improving the safety profile of drug candidates and crop protection molecules is most useful when it identifies relevant biological and mechanistic information that highlights risks and informs risk mitigation strategies. Pathway-based approaches, such as gene set enrichment analysis, integrate toxicogenomic data with known biological process and pathways. Network methods help define unknown biological processes and offer data reduction advantages. Integrating the 2 approaches would improve interpretation of toxicogenomic information. Barriers to the routine application of these methods in genome-wide transcriptomic studies include a need for "hands-on" computer programming experience, the selection of 1 or more analysis methods (eg pathway analysis methods), the sensitivity of results to algorithm parameters, and challenges in linking differential gene expression to variation in safety outcomes. To facilitate adoption and reproducibility of gene expression analysis in safety studies, we have developed Collaborative Toxicogeomics, an open-access integrated web portal using the Django web framework. The software, developed with the Python programming language, is modular, extensible and implements "best-practice" methods in computational biology. New study results are compared with over 4000 rodent liver experiments from Drug Matrix and open TG-GATEs. A unique feature of the software is the ability to integrate clinical chemistry and histopathology-derived outcomes with results from gene expression studies, leading to relevant mechanistic conclusions. We describe its application by analyzing the effects of several toxicants on liver gene expression and exemplify application to predicting toxicity study outcomes upon chronic treatment from expression changes in acute-duration studies.

Indexed as

Access to InformationInternetToxicogeneticsBenzbromaroneBenzofuransHumansLiverOmeprazolePhenotypeTranscriptomeTriglyceridesBenzbromaronebenziodaroneBenzofuransOmeprazoleTriglyceridesgene expression analysismechanism inferencesystems biologytoxicity predictiontoxicogenomics

Identifiers

PMID31020328
PMCPMC6657575
OpenAlexW2942183044

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.