Evidence map›Paper›PMID 40059972›Full record

ArticleToxicology research2025

Do the azo food colorings carmoisine and ponceau 4R have a genotoxic potential?

Sadriye Gokce Kara, Deniz Yuzbasioglu, Ece Avuloglu-Yilmaz, Fatma Unal

Abstract read
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Article in Toxicology research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Review
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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.

Sadriye Gokce KaraGazi University, Science Faculty, Department of Biology, Genetic Toxicology Laboratory, Ankara, 06170, Turkey.ORCID https://orcid.org/0000-0002-5177-2911
Deniz YuzbasiogluGazi University, Science Faculty, Department of Biology, Genetic Toxicology Laboratory, Ankara, 06170, Turkey.ORCID https://orcid.org/0000-0003-2756-7712
Ece Avuloglu-YilmazAmasya University, School of Technical Sciences, Department of Health Information Systems, Amasya, 05000, Turkey.ORCID https://orcid.org/0000-0002-5164-3431
Fatma UnalGazi University, Science Faculty, Department of Biology, Genetic Toxicology Laboratory, Ankara, 06170, Turkey.ORCID https://orcid.org/0000-0002-7468-6186

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Today, ready-to-eat foods to which various additives are frequently added are widely consumed. Food colorings constitute an essential part of these additives. Carmoisine (E-122) and Ponceau 4R (E-124) are the most commonly used azo food colorings. This study aimed to investigate the in vitro genotoxic effects of these two food dyes in human peripheral lymphocytes using four different and complementary genotoxicity tests (chromosome aberrations (CAs), sister chromatid exchange (SCEs), cytokinesis block micronucleus cytome (CBMN-Cyt) and comet). When four different concentrations (37.5, 75, 150, and 300 μg/mL) of both food dyes were applied to lymphocytes for 24 and 48 h, it was observed that only the highest concentration significantly increased the frequencies of CA and SCE. The mitotic index (MI) decreased compared to the control at all concentrations except the lowest one in the 24-h treatment of Carmoisine and the two highest concentrations (150, 300 μg/mL) in the 48-h treatment. In the 24-h Ponceau 4R treatment, MI decreased compared to the control at all concentrations except the lowest and all concentrations in the 48-h treatment. In contrast, Carmoisine and Ponceau 4R did not affect MN frequency. In the comet test, Carmoisine increased tail length only at the highest concentration, and Ponceau 4R increased tail length at the two highest concentrations. Ponceau 4R also increased tail moment only at the highest concentration. When the results of these four in vitro genotoxicity tests were evaluated together, it was concluded that both food colors were genotoxic, especially at high concentrations, but not at low concentrations.

Indexed as

Carmoisinegenotoxicityhuman lymphocytesIn vitroPonceau 4R

Identifiers

PMID40059972
PMCPMC11890108

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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.