Evidence map›Paper›PMID 42666318›Full record

ArticleFrontiers in pharmacology2026

Anticancer potential of

Julia Sroka, Mikołaj Jacyno, Dariusz Nowicki, Wojciech Makowski, Agnieszka Szopa, Paweł Kubica, Aleksandra Królicka, Małgorzata Stasiłojć

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. 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

8 authors.

Julia SrokaLaboratory of Biologically Active Compounds, Intercollegiate Faculty of Biotechnology UG and MUG, University of Gdansk, Gdansk, Poland.
Mikołaj JacynoDepartment of Immunology, Mossakowski Medical Research Institute, Polish Academy of Sciences, Warsaw, Poland.
Dariusz NowickiDepartment of Bacterial Molecular Genetics, Faculty of Biology, University of Gdansk, Gdansk, Poland.
Wojciech MakowskiDepartment of Botany, Physiology and Plant Protection, Faculty of Biotechnology and Horticulture, University of Agriculture in Kraków, Kraków, Poland.
Agnieszka SzopaDepartment of Medicinal Plant and Mushroom Biotechnology, Jagiellonian University Medical College, Kraków, Poland.
Paweł KubicaDepartment of Medicinal Plant and Mushroom Biotechnology, Jagiellonian University Medical College, Kraków, Poland.
Aleksandra KrólickaLaboratory of Biologically Active Compounds, Intercollegiate Faculty of Biotechnology UG and MUG, University of Gdansk, Gdansk, Poland.
Małgorzata StasiłojćDepartment of Cell Biology and Immunology, Intercollegiate Faculty of Biotechnology UG and MUG, Medical University of Gdansk, Gdansk, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Plant-derived polyphenols, including catechins, have been extensively studied for their anticancer properties for years. However, complex plant extracts may exhibit enhanced activity compared to isolated compounds owing to synergistic/additive phytochemical interactions. To date, the anticancer potential of extracts from Purpose: This study aimed to evaluate the anticancer activity of Methods: Methanolic root extracts and pure catechins were tested against five human cancer cell lines (A549, MDA-MB-231, Ramos, Namalwa, Raji) and human fibroblasts (BJ) as a control using the MTT assay. The mode of cell death was assessed by flow cytometry and Annexin V-FITC/PI staining. Results: The root extract induced a reduction in cancer cell viability comparable to that observed for isolated catechins, despite containing substantially lower concentrations of these compounds. This effect was most pronounced in lymphoma cells, which showed the highest sensitivity to extract treatment. Flow cytometric analysis indicated that the extract predominantly triggered apoptotic cell death. Conclusion: Despite its low catechin concentration, the extract from roots of

Indexed as

apoptosiscatechinsGalleria mellonellaJapanese knotweedlymphomasecondary metabolites

Identifiers

PMID42666318
PMCPMC13522145

What OpenQuestion holds

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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.