Evidence map›Paper›PMID 30846532›Full record

ArticleGenome research2019

Experimental and pan-cancer genome analyses reveal widespread contribution of acrylamide exposure to carcinogenesis in humans.

Maria Zhivagui, Alvin W T Ng, Maude Ardin, Mona I Churchwell, Manuraj Pandey, Claire Renard, Stephanie Villar, Vincent Cahais, Alexis Robitaille, Liacine Bouaoun and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
–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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 88 citations in OpenAlex.

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  20. Assessment of the genotoxicity of acrylamide.EFSA journal. European Food Safety Authority · 2022
    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

20 authors at 6 institutions in 5 countries.

Maria ZhivaguiMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Alvin W T NgCentre for Computational Biology, Duke-NUS Medical School, Singapore 169857, Singapore.
Maude ArdinMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Mona I ChurchwellDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, Arkansas 72079, USA.
Manuraj PandeyMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Claire RenardMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Stephanie VillarMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Vincent CahaisEpigenetics Group, International Agency for Research on Cancer, Lyon 69008, France.
Alexis RobitailleInfections and Cancer Biology Group, International Agency for Research on Cancer, Lyon 69008, France.
Liacine BouaounEnvironment and Radiation Section, International Agency for Research on Cancer, Lyon 69008, France.
Adriana HeguyDepartment of Pathology and Genome Technology Center, New York University, Langone Medical Center, New York, New York 10016, USA.
Kathryn Z GuytonIARC Monographs Group, International Agency for Research on Cancer, Lyon 69008, France.
Martha R StampferBiological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
James McKayGenetic Cancer Susceptibility Group, International Agency for Research on Cancer, Lyon 69008, France.
Monica HollsteinMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Magali OlivierMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Steven G RozenCentre for Computational Biology, Duke-NUS Medical School, Singapore 169857, Singapore.
Frederick A BelandDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, Arkansas 72079, USA.
Michael KorenjakMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Jiri ZavadilMolecular Mechanisms and Biomarkers Group, International Agency for Research on Cancer, Lyon 69008, France.
Centre international de recherche sur le cancer · FRDuke-NUS Medical School · SGNational Center for Toxicological Research · USLawrence Berkeley National Laboratory · USNYU Langone Health · USUniversity of Leeds · GB

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Modeling mutational landscapes of primary cancers using an in vitro cell immortalization assayR03ES025023 · NIEHS · INTERNATIONAL AGENCY FOR RES ON CANCER · PI OLIVIER, MAGALI · 2015 to 2016
$113k
NCI NIH HHS P30 CA016087NIEHS NIH HHS R03 ES025023World Health Organization 001
6 · The paper itself

Abstract

Humans are frequently exposed to acrylamide, a probable human carcinogen found in commonplace sources such as most heated starchy foods or tobacco smoke. Prior evidence has shown that acrylamide causes cancer in rodents, yet epidemiological studies conducted to date are limited and, thus far, have yielded inconclusive data on association of human cancers with acrylamide exposure. In this study, we experimentally identify a novel and unique mutational signature imprinted by acrylamide through the effects of its reactive metabolite glycidamide. We next show that the glycidamide mutational signature is found in a full one-third of approximately 1600 tumor genomes corresponding to 19 human tumor types from 14 organs. The highest enrichment of the glycidamide signature was observed in the cancers of the lung (88% of the interrogated tumors), liver (73%), kidney (>70%), bile duct (57%), cervix (50%), and, to a lesser extent, additional cancer types. Overall, our study reveals an unexpectedly extensive contribution of acrylamide-associated mutagenesis to human cancers.

Indexed as

Environmental ExposureMutationAcrylamidesAnimalsCarcinogenesisCells, CulturedEpoxy CompoundsGenome, HumanHumansMiceMutagensNeoplasmsTumor Suppressor Protein p53AcrylamidesEpoxy CompoundsglycidamideMutagensTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID30846532
PMCPMC6442384
OpenAlexW2922482538

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.