Evidence map›Paper›PMID 41505431›Full record

ArticlePloS one2026

Phytochemical profiling and anticancer activity of the n-butanol fraction from Ardisia villosa extract: Inhibition of gastric cancer cell proliferation via cell cycle arrest and senescence induction.

Nguyet Mai Hua, Van Khang Pham, Thi Thanh Huong Le, Son Hiep Pham, Viet Hoang, Thu Huong Trinh, Dinh Quang Hung Can, Van Hung Hoang, Phu Hung Nguyen

Abstract read
In one paragraph

Article in PloS one, 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
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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

9 authors.

Nguyet Mai HuaFaculty of Natural Science and technology, TNU- University of Sciences, Thai Nguyen Province, Vietnam.
Van Khang PhamFaculty of Chemistry, TNU - University of Education, Thai Nguyen Province, Vietnam.
Thi Thanh Huong LeFaculty of Natural Science and technology, TNU- University of Sciences, Thai Nguyen Province, Vietnam.
Son Hiep PhamFaculty of Chemistry, TNU - University of Education, Thai Nguyen Province, Vietnam.
Viet HoangInstitute for Excellence in Education and Research, Thai Nguyen University (TNU), Thai Nguyen Province, Vietnam.
Thu Huong TrinhInstitute for Excellence in Education and Research, Thai Nguyen University (TNU), Thai Nguyen Province, Vietnam.
Dinh Quang Hung CanInstitute for Excellence in Education and Research, Thai Nguyen University (TNU), Thai Nguyen Province, Vietnam.
Van Hung HoangThai Nguyen University, Thai Nguyen province, Vietnam.
Phu Hung NguyenInstitute for Excellence in Education and Research, Thai Nguyen University (TNU), Thai Nguyen Province, Vietnam.ORCID https://orcid.org/0009-0004-3130-6405

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medicinal plants serve as valuable sources for anticancer drug discovery. This study investigated the anticancer potential of the n-butanol fraction from Ardisia villosa extract against breast and gastric cancer cell lines. Phytochemical profiling using UPLC-QToF-MS in both positive and negative ESI modes identified 118 putative compounds, including flavonoids, lignans, alkaloids, triterpenoids, steroids, coumarins, and phenolic acids. The n-butanol fraction exhibited dose-dependent antiproliferative effects, with IC50 values of 60.2 µg/mL (MCF-7), 85.2 µg/mL (MKN45), and 51.7 µg/mL (AGS). In AGS gastric cancer cells, the extract significantly inhibited 3D tumorsphere formation and suppressed cell migration at concentrations as low as 50 µg/mL (p < 0.001). Additionally, n-butanol fraction extract markedly induced cellular senescence (p < 0.01). Mechanistic investigations revealed that the extract induced G0/G1 phase arrest by downregulating critical cell cycle regulators, including CCND1, CCNE1, CDK2, CDK3, CDK6, CDK8, and CDK9, while upregulating tumor suppressor and senescence-related genes such as p21, p53, p16, and p27 (p < 0.01). Molecular docking analyses further supported these findings by demonstrating strong binding affinities of phytochemicals to key cell cycle regulatory proteins, suggesting a direct molecular basis for their antiproliferative effects. In conclusion, the n-butanol fraction of Ardisia villosa displays potent anticancer activity, particularly in gastric cancer cells, through multi-targeted mechanisms involving cell cycle inhibition and senescence induction, and holds promise as a natural source for future anticancer therapeutics.

Indexed as

1-ButanolAntineoplastic Agents, PhytogenicArdisiaCell Cycle CheckpointsCellular SenescencePhytochemicalsPlant ExtractsStomach NeoplasmsCell Line, TumorCell MovementCell ProliferationHumansMolecular Docking Simulation1-ButanolAntineoplastic Agents, PhytogenicPhytochemicalsPlant Extracts

Identifiers

PMID41505431
PMCPMC12782380

What Socratic holds

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LicenceCC BY
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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 Socratic graph.