Evidence map›Paper›PMID 38731832›Full record

ArticleInternational journal of molecular sciences2024

Cytotoxic Potential of the Monoterpene Isoespintanol against Human Tumor Cell Lines.

Orfa Inés Contreras-Martínez, Alberto Angulo-Ortíz, Gilmar Santafé Patiño, Fillipe Vieira Rocha, Karine Zanotti, Dario Batista Fortaleza, Tamara Teixeira, Jesus Sierra Martinez

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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

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

1 citing paper in PubMed.

  1. Article
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.

Orfa Inés Contreras-MartínezBiology Department, Faculty of Basic Sciences, University of Córdoba, Montería 230002, Colombia.ORCID 0000-0001-5056-4355
Alberto Angulo-OrtízChemistry Department, Faculty of Basic Sciences, University of Córdoba, Montería 230002, Colombia.
Gilmar Santafé PatiñoChemistry Department, Faculty of Basic Sciences, University of Córdoba, Montería 230002, Colombia.ORCID 0000-0002-9235-3844
Fillipe Vieira RochaChemistry Department, Federal University of São Carlos, São Carlos 13565-905, Brazil.ORCID 0000-0002-5117-871X
Karine ZanottiChemistry Department, Federal University of São Carlos, São Carlos 13565-905, Brazil.ORCID 0000-0003-1121-8366
Dario Batista FortalezaChemistry Department, Federal University of São Carlos, São Carlos 13565-905, Brazil.
Tamara TeixeiraChemistry Department, Federal University of São Carlos, São Carlos 13565-905, Brazil.ORCID 0000-0003-3227-9395
Jesus Sierra MartinezGenetics and Evolution Department, Federal University of São Carlos, São Carlos 13565-905, Brazil.ORCID 0000-0002-7799-0212

Funding

Federal University of São Carlos 2022/02876-0 FAPESPUniversity of Córdoba FCB-02-19 project
6 · The paper itself

Abstract

Cancer is a disease that encompasses multiple and different malignant conditions and is among the leading causes of death in the world. Therefore, the search for new pharmacotherapeutic options and potential candidates that can be used as treatments or adjuvants to control this disease is urgent. Natural products, especially those obtained from plants, have played an important role as a source of specialized metabolites with recognized pharmacological properties against cancer, therefore, they are an excellent alternative to be used. The objective of this research was to evaluate the action of the monoterpene isoespintanol (ISO) against the human tumor cell lines MDA-MB-231, A549, DU145, A2780, A2780-cis and the non-tumor line MRC-5. Experiments with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and fluorescence with propidium iodide (PI), 4',6-diamidino-2-phenylindole dilactate (DAPI) and green plasma revealed the cytotoxicity of ISO against these cells; furthermore, morphological and chromogenic studies revealed the action of ISO on cell morphology and the inhibitory capacity on reproductive viability to form colonies in MDA-MB-231 cells. Likewise, 3D experiments validated the damage in these cells caused by this monoterpene. These results serve as a basis for progress in studies of the mechanisms of action of these compounds and the development of derivatives or synthetic analogues with a better antitumor profile.

Indexed as

MonoterpenesAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCell SurvivalHumansAntineoplastic AgentsMonoterpenesantitumor activitycell linesisoespintanolmonoterpene

Identifiers

PMID38731832
PMCPMC11083712

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.