Evidence map›Paper›PMID 36949493›Full record

ArticleGenes and environment : the official journal of the Japanese Environmental Mutagen Society2023

Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila.

Megumi Toyoshima-Sasatani, Fumika Imura, Yuko Hamatake, Akihiro Fukunaga, Tomoe Negishi

Open access · goldFull text read
In one paragraph

Article in Genes and environment : the official journal of the Japanese Environmental Mutagen Society, 2023. 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
0.9field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Megumi Toyoshima-Sasatani *Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Tsushima, 700-8530, Japan.
Fumika Imura *Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Tsushima, 700-8530, Japan.
Yuko HamatakeGraduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Tsushima, 700-8530, Japan.
Akihiro FukunagaSchool of Nursing, Osaka City University, Abeno-Ku, Osaka, 545-0051, Japan.
Tomoe NegishiGraduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Tsushima, 700-8530, Japan. tomoeisaka@gmail.com.ORCID http://orcid.org/0000-0002-3339-0784
Okayama University · JPHiroshima University · JPOsaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApoptotic cell death is an important survival system for multicellular organisms because it removes damaged cells. Mutation is also a survival method for dealing with damaged cells in multicellular and also unicellular organisms, when DNA lesions are not removed. However, to the best of our knowledge, no reports have comprehensively explored the direct relationship between apoptosis and somatic cell mutations induced by various mutagenic factors.

resultsMutation was examined by the wing-spot test, which is used to detect somatic cell mutations, including chromosomal recombination. Apoptosis was observed in the wing discs by acridine orange staining in situ. After treatment with chemical mutagens, ultraviolet light (UV), and X-ray, both the apoptotic frequency and mutagenic activity increased in a dose-dependent manner at non-toxic doses. When we used DNA repair-deficient Drosophila strains, the correlation coefficient of the relationship between apoptosis and mutagenicity, differed from that of the wild-type. To explore how apoptosis affects the behavior of mutated cells, we determined the spot size, i.e., the number of mutated cells in a spot. In parallel with an increase in apoptosis, the spot size increased with MNU or X-ray treatment dose-dependently; however, this increase was not seen with UV irradiation. In addition, BrdU incorporation, an indicator of cell proliferation, in the wing discs was suppressed at 6 h, with peak at 12 h post-treatment with X-ray, and that it started to increase again at 24 h; however, this was not seen with UV irradiation.

conclusionDamage-induced apoptosis and mutation might be coordinated with each other, and the frequency of apoptosis and mutagenicity are balanced depending on the type of DNA damage. From the data of the spot size and BrdU incorporation, it is possible that mutated cells replace apoptotic cells due to their high frequency of cell division, resulting in enlargement of the spot size after MNU or X-ray treatment. We consider that the induction of mutation, apoptosis, and/or cell growth varies in multi-cellular organisms depending on the type of the mutagens, and that their balance and coordination have an important function to counter DNA damage for the survival of the organism.

Indexed as

Acridine orangeAlkylating agentsApoptosisBrdUDrosophilaLarval wing discMutationTobacco smokeUltravioletX-ray

Identifiers

PMID36949493
PMCPMC10035180
OpenAlexW4353046298

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read25
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.