Evidence map›Paper›PMID 42773735›Full record

ArticleChemistry & biodiversity2026

Phytochemical Analysis Using LC-MS/MS and Anticancer Activity of Asphodelus tenuifolius Roots: Cell Cycle Arrest, Apoptosis, and In Silico Insights.

Racha Lydia Bouchouka, Farida Larit, Zahia Kabouche, Marlène Debiossat, Laurent Riou, Catherine Ghezzi, Francisco León, Ahmed Kabouche

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 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.

Racha Lydia BouchoukaLaboratoire D'obtention de Substances Thérapeutiques (LOST), Université Constantine 1-Frères Mentouri, Constantine, Algeria.ORCID https://orcid.org/0000-0002-0561-2415
Farida LaritLaboratoire D'obtention de Substances Thérapeutiques (LOST), Université Constantine 1-Frères Mentouri, Constantine, Algeria.ORCID https://orcid.org/0000-0002-1396-0719
Zahia KaboucheLaboratoire D'obtention de Substances Thérapeutiques (LOST), Université Constantine 1-Frères Mentouri, Constantine, Algeria.
Marlène DebiossatUniversité de Grenoble Alpes, Grenoble, France.ORCID https://orcid.org/0009-0005-1361-8023
Laurent RiouUniversité de Grenoble Alpes, Grenoble, France.ORCID https://orcid.org/0000-0002-9240-4680
Catherine GhezziUniversité de Grenoble Alpes, Grenoble, France.ORCID https://orcid.org/0000-0001-6840-400X
Francisco LeónDepartment of Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina, Columbia, South Carolina, USA.ORCID https://orcid.org/0000-0002-5064-2381
Ahmed KaboucheLaboratoire D'obtention de Substances Thérapeutiques (LOST), Université Constantine 1-Frères Mentouri, Constantine, Algeria.ORCID https://orcid.org/0000-0002-3738-6387

Funding

Laboratoire Radiopharmaceutiques Biocliniques LRB France
6 · The paper itself

Abstract

Asphodelus tenuifolius Cav. (Asphodelaceae) is traditionally used in North African ethnomedicine for inflammatory and oxidative stress-related disorders. In this study, the hydroethanolic root extract was investigated by LC-HRMS/MS, leading to the identification of 58 metabolites, mainly flavonoids, anthraquinones, and cinnamic acid derivatives. Major constituents included luteolin, emodin, luteolin-7-O-β-D-glucoside, subaphyllin (N-trans-feruloylputrescine), and N-trans-feruloyltyramine. The extract showed moderate antiproliferative activity against MDA-MB-231 and PC-3 cells, while flow cytometry revealed pronounced apoptosis induction (up to 85%) and significant G0/G1 cell-cycle arrest. Molecular docking and target prediction suggested multitarget modulation of ERα, AR, AKT1, CDK2, and BCL-2, particularly by aglycone metabolites. ADMET analysis indicated favorable drug-likeness and safety profiles. These findings provide the first mechanistic evidence supporting the multitarget anticancer potential of A. tenuifolius roots and highlight their value as a source of bioactive anticancer scaffolds.

Indexed as

Antineoplastic Agents, PhytogenicApoptosisAsphodelaceaeCell Cycle CheckpointsPhytochemicalsPlant ExtractsPlant RootsCell Line, TumorCell ProliferationChromatography, LiquidDrug Screening Assays, AntitumorHumansMolecular Docking SimulationTandem Mass SpectrometryAntineoplastic Agents, PhytogenicPhytochemicalsPlant Extractsanticancer activityapoptosisAsphodelus tenuifoliusLC–HRMS/MSmolecular docking

Identifiers

PMID42773735
PMCPMC13598352

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.