Evidence map›Paper›PMID 41697297›Full record

ArticleDie Naturwissenschaften2026

Potent anticancer activity of phenolic-enriched extracts from endemic plants supported by in vitro pharmacological analyses and in silico molecular docking.

Bugrahan Emsen, Mustafa Cicek, Burak Surmen, Hacer Sibel Karapinar

Abstract read
In one paragraph

Article in Die Naturwissenschaften, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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.

Bugrahan EmsenDepartment of Biology, Kamil Özdağ Faculty of Science, Karamanoğlu Mehmetbey University, Karaman, Türkiye. bugrahanemsen@gmail.com.
Mustafa CicekDepartment of Biology, Kamil Özdağ Faculty of Science, Karamanoğlu Mehmetbey University, Karaman, Türkiye.
Burak SurmenDepartment of Biology, Kamil Özdağ Faculty of Science, Karamanoğlu Mehmetbey University, Karaman, Türkiye.
Hacer Sibel KarapinarDepartment of Chemistry, Kamil Özdağ Faculty of Science, Karamanoğlu Mehmetbey University, Karaman, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the present study, methanol and aqueous extracts obtained from two endemic plants, Dianthus elegans var. actinopetalus (Fenzl) Reeve and Linum ciliatum Hayek, were investigated for their phenolic composition, antioxidant activities, cytotoxic potential, and supported by in silico molecular docking analysis. High-performance liquid chromatography revealed distinct phenolic acid and flavonoid profiles among the extracts, with the methanol extract of L. ciliatum (LME) exhibiting the richest phenolic content. Consistently, LME showed the highest total phenol (314.69 µg/mg) and total flavonoid (91.61 µg/mg) levels. Antioxidant capacity was evaluated using DPPH radical scavenging and metal chelation assays, in which LME demonstrated the strongest activity with the lowest IC₅₀ values (45.49 and 40.10 µg/mL, respectively), highlighting the influence of extraction solvent on bioactivity. Cytotoxic effects were assessed on Mahlavu and MCF-7 cell lines at 24, 48, and 72 h. Both methanol and aqueous extracts of L. ciliatum exhibited time-dependent cytotoxicity, with LME showing a remarkably low IC₅₀ value of 0.66 µg/mL on MCF-7 cells after 72 h. To gain insight into the molecular basis of the observed cytotoxic effects, in silico molecular docking was performed using the anti-apoptotic Bcl-2 protein as a target. The major phenolic compounds, particularly chlorogenic acid, quercetin, and naringenin, exhibited strong binding affinities toward Bcl-2, suggesting a possible involvement of apoptosis-related pathways. In contrast, none of the extracts showed antibacterial activity against the tested Gram-positive or Gram-negative bacteria. Overall, the findings indicate that methanol extraction is more effective for obtaining phenolic-rich extracts with pronounced antioxidant and anticancer potential.

Indexed as

Antineoplastic AgentsAntineoplastic Agents, PhytogenicMolecular Docking SimulationPhenolsPlant ExtractsAntioxidantsCell Line, TumorFlavonoidsHumansMCF-7 CellsAntineoplastic AgentsAntineoplastic Agents, PhytogenicAntioxidantsFlavonoidsPhenolsPlant ExtractsBioactive compoundsPharmaceutical potentialPhytochemicalsPhytotherapyPolyphenols

Identifiers

PMID41697297
PMCPMC12909422

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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.