Evidence map›Paper›PMID 37643630›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2023

A mode of action-based probabilistic framework of dose-response assessment for nonmutagenic liver carcinogens: a case study of PCB-126.

Yun Zhou, Qiran Chen, James E Klaunig, Kan Shao

Open access · hybridAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 31% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 1 country.

Yun ZhouDepartment of Environmental and Occupational Health, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana 47405, USA.
Qiran ChenDepartment of Environmental and Global Health, College of Public Health and Health Professions, University of Florida, Gainesville, Florida 32610, USA.
James E KlaunigDepartment of Environmental and Occupational Health, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana 47405, USA.
Kan ShaoDepartment of Environmental and Occupational Health, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana 47405, USA.
Indiana University Bloomington · USUniversity of Florida · US

Funding

Quantitative dose-response characterization for liver carcinogenicity with non-mutagenic modes of actionK25ES030402 · NIEHS · TRUSTEES OF INDIANA UNIVERSITY · PI SHAO, KAN · 2020 to 2024
$764k
NIEHS NIH HHSNIEHS NIH HHS K25 ES030402NIH HHS K25ES030402
6 · The paper itself

Abstract

A main function of dose-response assessment is to estimate a "safe" dose in the target population to support chemical risk assessment. Typically, a "safe" dose is developed differently for cancer and noncancer effects based on a 2-step procedure, ie, point of departure (POD) derivation and low-dose extrapolation. However, the current dose-response assessment framework is criticized for its dichotomized strategy without integrating the mode of action (MOA) information. The objective of this study was, based on our previous work, to develop a MOA-based probabilistic dose-response framework that quantitatively synthesizes a biological pathway in a dose-response modeling process to estimate the risk of chemicals that have carcinogenic potential. 3,3',4,4',5-Pentachlorobiphenyl (PCB-126) was exemplified to demonstrate our proposed approach. There were 4 major steps in the new modeling framework, including (1) key quantifiable events (KQEs) identification and extraction, (2) essential dose calculation, (3) MOA-based POD derivation, and (4) MOA-based probabilistic reference dose (RfD) estimation. Compared with reported PODs and traditional RfDs, the MOA-based estimates derived from our approach were comparable and plausible. One key feature of our approach was the use of overall MOA information to build the dose-response relationship on the entire dose continuum including the low-dose region. On the other hand, by adjusting uncertainty and variability in a probabilistic manner, the MOA-based probabilistic RfDs can provide useful insights of health protection for the specific proportion of population. Moreover, the proposed framework had important potential to be generalized to assess different types of chemicals other than nonmutagenic carcinogens, highlighting its utility to improve current chemical risk assessment.

Indexed as

NeoplasmsCarcinogenesisCarcinogensDose-Response Relationship, DrugHumansLiverPolychlorinated BiphenylsRisk Assessment3,4,5,3',4'-pentachlorobiphenylCarcinogensPolychlorinated BiphenylsMOAnonmutagenic carcinogensPCB-126probabilistic dose-response

Identifiers

PMID37643630
PMCPMC10682966
OpenAlexW4386241072

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.