Evidence map›Paper›PMID 42386920›Full record

ArticleScientific reports2026

Integrated metabolomic, cytotoxic, and computational investigation of Caralluma tuberculata extract in breast cancer cells.

Amir Ali, Rodolfo Moreno-Castillo, Luis Cordova-Bahena, Carlos Martín Cerda-García-Rojas, Zia-Ur-Rehman Mashwani, Edgar Hernández-Martínez, Juan Pedro Luna-Arias

Abstract read
In one paragraph

Article in Scientific reports, 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

7 authors.

Amir AliNanoscience and Nanotechnology PhD Program, Department of Research and Multidisciplinary Studies, Center for Research and Advanced Studies (Cinvestav), Av. IPN 2508, Col. San Pedro Zacatenco, Alcaldía Gustavo A. Madero, C.P. 07360, Mexico City, Mexico.
Rodolfo Moreno-CastilloDepartment of Cell Biology, Center for Research and Advanced Studies (Cinvestav), Av. IPN 2508, Col. San Pedro Zacatenco, Alcaldía Gustavo A. Madero, C.P. 07360, Mexico City, Mexico.
Luis Cordova-BahenaFaculty of Medicine, National Autonomous University of Mexico (Universidad Nacional Autónoma de México, UNAM), 04510, Mexico City, Mexico.
Carlos Martín Cerda-García-RojasDepartment of Chemistry, Center for Research and Advanced Studies (Cinvestav), Av. IPN 2508, Col. San Pedro Zacatenco, Alcaldía Gustavo A. Madero, C.P. 07360, Mexico City, Mexico.
Zia-Ur-Rehman MashwaniDepartment of Botany, Pir Mehr Ali Shah Arid (PMAS) Agriculture University, Arid Agriculture University Rawalpindi, Rawalpindi, Pakistan.
Edgar Hernández-MartínezDepartment of Cell Biology, Center for Research and Advanced Studies (Cinvestav), Av. IPN 2508, Col. San Pedro Zacatenco, Alcaldía Gustavo A. Madero, C.P. 07360, Mexico City, Mexico.
Juan Pedro Luna-AriasNanoscience and Nanotechnology PhD Program, Department of Research and Multidisciplinary Studies, Center for Research and Advanced Studies (Cinvestav), Av. IPN 2508, Col. San Pedro Zacatenco, Alcaldía Gustavo A. Madero, C.P. 07360, Mexico City, Mexico. jpluna@cinvestav.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Caralluma tuberculata, belonging to the family Apocynaceae, is widely used in folk medicine for the management of diseases such as diabetes and cancer, owing to its rich secondary metabolite profile. This study aimed to explore the metabolites of C. tuberculata and evaluate their anti-breast cancer activity using high-performance liquid chromatography (HPLC), Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS), and the MTT assay. HPLC and LC-ESI-MS/MS analyses revealed major bioactive peaks at 17-22 and 45-80 min, indicating a high diversity of phytoconstituents. Metabolomic analysis identified 60 phytochemicals, highlighting the plant as a rich source of compounds with potential pharmacological relevance. Moreover, the extract exhibited selective cytotoxicity against MDA-MB-231 breast cancer cells (44% reduction in viability) while exerting comparatively lower effects on non-tumorigenic MCF-12F breast cells (22%), suggesting its potential as a source of bioactive compounds. To explore potential molecular targets associated with these effects, the identified metabolites were evaluated for their interactions with carnitine palmitoyltransferase 1A (CPT1A) using molecular docking. Among them, diosmetin and luteolin showed the strongest binding affinities and favorable safety profiles. Molecular dynamics simulations of these selected compounds further supported the stability of their interactions with CPT1A. These findings highlight diosmetin and luteolin as promising candidates for further investigation as potential modulators of CPT1A in breast cancer.

Indexed as

Antineoplastic Agents, PhytogenicApocynaceaeBreast NeoplasmsMetabolomicsPlant ExtractsCarnitine O-PalmitoyltransferaseCell Line, TumorCell SurvivalChromatography, High Pressure LiquidFemaleHumansMDA-MB-231 CellsMolecular Docking SimulationTandem Mass SpectrometryAntineoplastic Agents, PhytogenicCarnitine O-PalmitoyltransferasePlant ExtractsBreast cancerCaralluma tuberculataCPT1ADiosmetinFlavonoidsLC–ESI–MS/MSLuteolinMetabolomicsMolecular dockingMolecular dynamics

Identifiers

PMID42386920
PMCPMC13482624

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.