Evidence map›Paper›PMID 38288963›Full record

ReviewToxicologic pathology2023

Toxicogenomics Approaches to Address Toxicity and Carcinogenicity in the Liver.

Arun R Pandiri, Scott S Auerbach, Jim L Stevens, Eric A G Blomme

Abstract readReview
In one paragraph

Review in Toxicologic pathology, 2023. 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
–field-weighted citation impact
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.

  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

4 authors.

Arun R PandiriNational Institute of Environmental Health Sciences, Durham, North Carolina, USA.ORCID 0000-0003-0963-9073
Scott S AuerbachNational Institute of Environmental Health Sciences, Durham, North Carolina, USA.
Jim L StevensUniversiteit Leiden, Leiden, The Netherlands.
Eric A G BlommeAbbVie, North Chicago, Illinois, USA.

Funding

Pathology Services Supporting the Division Translational ToxicologyZICES103376 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI CESTA, MARK · 2022 to 2025
$23.9M
ZIA CARCI Carcinogenicity Health Effects innovation Research ProgramZIAES103383 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI PANDIRI, ARUN KUMAR · 2022 to 2025
$13.0M
Molecular Pathogenesis of Rodent NeoplasiaZIAES103349 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI PANDIRI, ARUN KUMAR · 2020 to 2021
$5.4M
Intramural NIH HHS Z99 ES999999Intramural NIH HHS ZIA ES103349Intramural NIH HHS ZIA ES103383Intramural NIH HHS ZIC ES103376
6 · The paper itself

Abstract

Toxicogenomic technologies query the genome, transcriptome, proteome, and the epigenome in a variety of toxicological conditions. Due to practical considerations related to the dynamic range of the assays, sensitivity, cost, and technological limitations, transcriptomic approaches are predominantly used in toxicogenomics. Toxicogenomics is being used to understand the mechanisms of toxicity and carcinogenicity, evaluate the translational relevance of toxicological responses from in vivo and in vitro models, and identify predictive biomarkers of disease and exposure. In this session, a brief overview of various transcriptomic technologies and practical considerations related to experimental design was provided. The advantages of gene network analyses to define mechanisms were also discussed. An assessment of the utility of toxicogenomic technologies in the environmental and pharmaceutical space showed that these technologies are being increasingly used to gain mechanistic insights and determining the translational relevance of adverse findings. Within the environmental toxicology area, there is a broader regulatory consideration of benchmark doses derived from toxicogenomics data. In contrast, these approaches are mainly used for internal decision-making in pharmaceutical development. Finally, the development and application of toxicogenomic signatures for prediction of apical endpoints of regulatory concern continues to be area of intense research.

Indexed as

LiverToxicogeneticsGene Expression ProfilingProteomicsTranscriptomecarcinogenicitylivermechanismstoxicitytoxicogenomics

Identifiers

PMID38288963
PMCPMC11014763

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.