Evidence map›Paper›PMID 25751783›Full record

ArticleMolecules (Basel, Switzerland)2015

Assessing chemical constituents of Mimosa caesalpiniifolia stem bark: possible bioactive components accountable for the cytotoxic effect of M. caesalpiniifolia on human tumour cell lines.

Nayana Bruna Nery Monção, Bruno Quirino Araújo, Jurandy do Nascimento Silva, Daisy Jereissati Barbosa Lima, Paulo Michel Pinheiro Ferreira, Flavia Pereira da Silva Airoldi, Cláudia Pessoa, Antonia Maria das Graças Lopes Citó

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

7 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  3. Review
  4. Review
  5. Article
  6. Article
  7. Acylphloroglucinol Derivatives fromMolecules (Basel, Switzerland) · 2018
    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 at 3 institutions in 1 country.

Nayana Bruna Nery MonçãoDepartment of Chemistry, Federal University of Piauí, Teresina 64049-550, PI, Brazil. nayaninhanery@hotmail.com.
Bruno Quirino AraújoDepartment of Chemistry, Federal University of Piauí, Teresina 64049-550, PI, Brazil. bquirinoa@hotmail.com.
Jurandy do Nascimento SilvaPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina 64049-550, PI, Brazil. jurandy@ifpi.edu.br.
Daisy Jereissati Barbosa LimaDepartment of Physiology and Pharmacology, Federal University of Ceará, Fortaleza 60430-270, CE, Brazil. daisylima@gmail.com.
Paulo Michel Pinheiro FerreiraPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina 64049-550, PI, Brazil. pmifepe@yahoo.com.br.
Flavia Pereira da Silva AiroldiLaboratory of Organic Geochemistry, University of Campinas, São Paulo 13083-970, SP, Brazil. flavia_aguayo@yahoo.com.br.
Cláudia PessoaDepartment of Physiology and Pharmacology, Federal University of Ceará, Fortaleza 60430-270, CE, Brazil. cpessoa@ufc.br.
Antonia Maria das Graças Lopes CitóDepartment of Chemistry, Federal University of Piauí, Teresina 64049-550, PI, Brazil. gracacito@gmail.com.
Universidade Federal do Piauí · BRUniversidade Federal do Ceará · BRUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mimosa caesalpiniifolia is a native plant of the Brazilian northeast, and few studies have investigated its chemical composition and biological significance. This work describes the identification of the first chemical constituents in the ethanolic extract and fractions of M. caesalpiniifolia stem bark based on NMR, GC-qMS and HRMS analyses, as well as an assessment of their cytotoxic activity. GC-qMS analysis showed fatty acid derivatives, triterpenes and steroid substances and confirmed the identity of the chemical compounds isolated from the hexane fraction. Metabolite biodiversity in M. caesalpiniifolia stem bark revealed the differentiated accumulation of pentacyclic triterpenic acids, with a high content of betulinic acid and minor amounts of 3-oxo and 3β-acetoxy derivatives. Bioactive analysis based on total phenolic and flavonoid content showed a high amount of these compounds in the ethanolic extract, and ESI-(-)-LTQ-Orbitrap-MS identified caffeoyl hexose at high intensity, as well as the presence of phenolic acids and flavonoids. Furthermore, the evaluation of the ethanolic extract and fractions, including betulinic acid, against colon (HCT-116), ovarian (OVCAR-8) and glioblastoma (SF-295) tumour cell lines showed that the crude extract, hexane and dichloromethane fractions possessed moderate to high inhibitory activity, which may be related to the abundance of betulinic acid. The phytochemical and biological study of M. caesalpiniifolia stem bark thus revealed a new alternative source of antitumour compounds, possibly made effective by the presence of betulinic acid and by chemical co-synergism with other compounds.

Indexed as

Antineoplastic Agents, PhytogenicBetulinic AcidCell SurvivalFlavonoidsHumansMimosaNeoplasmsPentacyclic TriterpenesPhenolsPlant BarkPlant ExtractsTriterpenesTumor Cells, CulturedAntineoplastic Agents, PhytogenicBetulinic AcidFlavonoidsPentacyclic TriterpenesPhenolsPlant ExtractsTriterpenes

Identifiers

PMID25751783
PMCPMC6272184
OpenAlexW2118696847

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.