Evidence map›Paper›PMID 35513806›Full record

ArticleGenes & nutrition2022

Impact of anthocyanin on genetic stability in mammary adenocarcinoma-induced mice treated with methotrexate.

Abeer A Khamis, Rana M Ibrahim, Gad B El-Hefnawy, Wafaa M Ibrahim, Ehab M Ali

Open access · goldAbstract read
In one paragraph

Article in Genes & nutrition, 2022. 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
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0citing papers in PubMed
–field-weighted citation impact, top 93% 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, 0 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

5 authors at 2 institutions in 2 countries.

Abeer A KhamisBiochemistry Division, Chemistry Department, Faculty of Science, Tanta University, Tanta, Egypt. abeer.khamis@science.tanta.edu.eg.ORCID https://orcid.org/0000-0001-5216-2712
Rana M IbrahimBiochemistry Division, Chemistry Department, Faculty of Science, Tanta University, Tanta, Egypt.
Gad B El-HefnawyBiochemistry Department, Faculty of Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Wafaa M IbrahimChemistry Department, Faculty of Science, Tanta University, Tanta, Egypt.
Ehab M AliBiochemistry Department, Faculty of Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Tanta University · EGKing Abdulaziz University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenetic instability leads to genome mutations, changes in nucleotide sequences, rearrangements, and gains or losses of part of the chromosomes. This instability can initiate and develop cancer. This study evaluated genomic stability in methotrexate and anthocyanin-treated mammary adenocarcinoma model. Seventy albino mice were divided into seven groups: negative control, anthocyanin, methotrexate, Ehrlich's solid tumor; Ehrlich's solid tumor and methotrexate; Ehrlich's solid tumor and anthocyanin; and Ehrlich's solid tumor, methotrexate, and anthocyanin groups.

resultsTumor weight and size were evaluated. Serum arylesterase activity was low in all the induced tumors and those treated with anthocyanin, methotrexate, or both. Poly[adenosine diphosphate (ADP)-ribose] polymerase activity was high, and glutathione S-transferase activity was low in the tumors treated with anthocyanin, methotrexate, or both, compared with that of the untreated tumor. There was an increase in DNA damage in the mice with solid tumors and those injected with methotrexate or methotrexate and anthocyanin, compared with that in the untreated mice.

conclusionsThere was a decrease in genetic instability and DNA damage in the tumor-bearing mice treated with anthocyanin, with a concomitant increase in nuclear poly[adenosine diphosphate (ADP)-ribose] polymerase activity, compared with those of the untreated group. Anthocyanin exerted positive effects in the treatment of mammary adenocarcinoma.

Indexed as

Antitumor drugDetoxifying enzymeDNA damageEhrlich’s solid tumorFlavonoidsPoly[adenosine diphosphate (ADP)-ribose] polymerase

Identifiers

PMID35513806
PMCPMC9074366
OpenAlexW4229042428

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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.