Evidence map›Paper›PMID 40493340›Full record

ArticleCell biochemistry and biophysics2025

Cytotoxic, Genotoxic, Apoptotic, and Reactive Oxygen Generating Properties of Bioactive Quinoline Derivatives as Novel Anti Breast Cancer Agents.

Vildan Betul Yenigun, Eray Metin Guler, Abdurrahim Kocyigit, Salih Ökten, Ezgi Balkan, Osman Çakmak

Abstract read
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In one paragraph

Article in Cell biochemistry and biophysics, 2025. 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
0cells of the map it votes in
0citing 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

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.

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

6 authors.

Vildan Betul YenigunBezmialem Vakıf University, Faculty of Medicine, Department of Medical Biochemistry, Istanbul, Türkiye.ORCID http://orcid.org/0000-0002-8021-8629
Eray Metin GulerBezmialem Vakıf University, Faculty of Medicine, Department of Medical Biochemistry, Istanbul, Türkiye.ORCID http://orcid.org/0000-0003-4351-1719
Abdurrahim KocyigitBezmialem Vakıf University, Faculty of Medicine, Department of Medical Biochemistry, Istanbul, Türkiye. akocyigit@bezmialem.edu.tr.ORCID http://orcid.org/0000-0003-2335-412X
Salih ÖktenKırıkkale University, Faculty of Education, Department of Mathematics and Science Education, Division of Science Education, Kırıkkale, Türkiye.ORCID http://orcid.org/0000-0001-9656-1803
Ezgi BalkanBezmialem Vakıf University, Faculty of Medicine, Department of Medical Biochemistry, Istanbul, Türkiye.ORCID http://orcid.org/0000-0002-0760-497X
Osman Çakmakİstanbul Rumeli University, Faculty of Arts and Design, Department of Gastronomy, İstanbul, Türkiye.ORCID http://orcid.org/0000-0001-9293-5572

Funding

Bezmialem Vakif University Scientific Research Projects Units 6.2017/55
6 · The paper itself

Abstract

The heterocyclic aromatic compound quinoline is widely used in pharmaceutical production due to its diverse biological activities, including anticancer properties. This study aimed to investigate the anticancer properties of newly synthesized quinoline derivatives: 5,7-dibromo-8-hydroxyquinoline (MC-5-2), 6,8-dibromotetrahydroquinoline (SO-3-3), nitroquinoline bromide (SO-22), and methoxyhydroxyquinoline bromide (SO-18) against breast cancer. Cytotoxic, genotoxic, apoptotic, and oxidative stress effects were assessed through ATP viability, comet, AO/EB staining, and H2DCF-DA assays using MCF-7 and MDA-MB-231 cancer cells and normal 184A1 breast epithelial cells. Intracellular glutathione levels were analyzed using the luminometric method using a GSH kit, and mitochondrial membrane potential through DiOC6(3) dye. ATP cell viability assay revealed significant reductions in cancer cell vitality with a lower impact on normal cells. MC-5-2 exhibited the highest cytotoxicity on MDA-MB-231 breast cancer cells, with the lowest IC

Indexed as

Antineoplastic AgentsApoptosisBreast NeoplasmsDNA DamageQuinolinesReactive Oxygen SpeciesCell Line, TumorCell SurvivalFemaleGlutathioneHumansMCF-7 CellsMembrane Potential, MitochondrialOxidative StressAntineoplastic AgentsGlutathioneQuinolinesReactive Oxygen SpeciesAnticancer ActivityApoptosisCytotoxicityGenotoxicityQuinolineROS

Identifiers

What OpenQuestion holds

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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.