Evidence map›Paper›PMID 10807553›Full record

ReviewEnvironmental health perspectives2000

Mutagenicity of trichloroethylene and its metabolites: implications for the risk assessment of trichloroethylene.

M M Moore, K Harrington-Brock

Open access · diamondAbstract readReview
In one paragraph

Review in Environmental health perspectives, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 65 citations in OpenAlex.

  1. Mutagenicity Assessment to Pesticide Adjuvants of Toluene, Chloroform, and Trichloroethylene by Ames Test.International journal of environmental research and public health · 2021
    Article
  2. Chemical Peels in Skin Cancer: A Review.The Journal of clinical and aesthetic dermatology · 2020
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. In vitro cytogenetic assessment of trichloroacetic acid in human peripheral blood lymphocytes.Environmental science and pollution research international · 2014
    Article
  9. Article
  10. Review
  11. Review
  12. TCE Meta-Analyses: Wartenberg et al.'s Response.Environmental health perspectives · 2000
    Article
  13. Re: "Collision of Evidence and Assumptions: TMI Déjà View"Environmental health perspectives · 2000
    Article
  14. Bisphenol A and Dental Sealants: Olea's Response.Environmental health perspectives · 2000
    Article
  15. Trichloroethylene health risks--state of the science.Environmental health perspectives · 2000
    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

2 authors at 1 institution in 1 country.

M M MooreU.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA. moore.martha@epa.gov
K Harrington-Brock
Environmental Protection Agency · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This article addresses the evidence that trichloroethylene (TCE) or its metabolites might mediate tumor formation via a mutagenic mode of action. We review and draw conclusions from the published mutagenicity and genotoxicity information for TCE and its metabolites, chloral hydrate (CH), dichloroacetic acid (DCA), trichloroacetic acid (TCA), trichloroethanol, S-(1, 2-dichlorovinyl)-l-cysteine (DCVC), and S-(1, 2-dichlorovinyl) glutathione (DCVG). The new U.S. Environmental Protection Agency proposed Cancer Risk Assessment Guidelines provide for an assessment of the key events involved in the development of specific tumors. Consistent with this thinking, we provide a new and general strategy for interpreting genotoxicity data that goes beyond a simple determination that the chemical is or is not genotoxic. For TCE, we conclude that the weight of the evidence argues that chemically induced mutation is unlikely to be a key event in the induction of human tumors that might be caused by TCE itself (as the parent compound) and its metabolites, CH, DCA, and TCA. This conclusion derives primarily from the fact that these chemicals require very high doses to be genotoxic. There is not enough information to draw any conclusions for trichloroethanol and the two trichloroethylene conjugates, DCVC and DCVG. There is some evidence that DCVC is a more potent mutagen than CH, DCA, or TCA. Unfortunately, definitive conclusions as to whether TCE will induce tumors in humans via a mutagenic mode of action cannot be drawn from the available information. More research, including the development and use of new techniques, is required before it is possible to make a definitive assessment as to whether chemically induced mutation is a key event in any human tumors resulting from exposure to TCE.

Indexed as

AnimalsCarcinogens, EnvironmentalDose-Response Relationship, DrugGenesHumansMutagensNeoplasmsRisk AssessmentTrichloroethyleneUnited StatesUnited States Environmental Protection AgencyCarcinogens, EnvironmentalMutagensTrichloroethylene

Identifiers

PMID10807553
PMCPMC1637765
OpenAlexW2017258713

What OpenQuestion holds

Textmetadata
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.