Evidence map›Paper›PMID 39109780›Full record

ArticleActa cirurgica brasileira2024

Anticancer, anti-inflammatory and analgesic activities of aminoalcohol-based quinoxaline small molecules.

Jannyely Moreira Neri, Paula Emília Apolônio Siqueira, Ana Luiza Cabral de Sá Leitão Oliveira, Renata Mendonça Araújo, Raimundo Fernandes de Araújo Júnior, Agnes Andrade Martins, Isabelle de Lima Marques, Rafaela Alcindo Silva, Aurigena Antunes de Araújo, Fabrício Gava Menezes

Abstract read
In one paragraph

Article in Acta cirurgica brasileira, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

10 authors.

Jannyely Moreira NeriUniversidade Federal do Rio Grande do Norte - Instituto de Química - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0003-4405-1523
Paula Emília Apolônio SiqueiraUniversidade Federal do Rio Grande do Norte - Departamento de Biomedicina - Natal (RN) - Brazil.ORCID http://orcid.org/0009-0005-4379-8256
Ana Luiza Cabral de Sá Leitão OliveiraUniversidade Federal do Rio Grande do Norte - Programa de Pós-Graduação em Ciências da Saúde - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0001-8692-9352
Renata Mendonça AraújoUniversidade Federal do Rio Grande do Norte - Instituto de Química - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0001-5514-5192
Raimundo Fernandes de Araújo JúniorUniversidade Federal do Rio Grande do Norte - Programa de Pós-Graduação em Ciências da Saúde - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0003-2349-2354
Agnes Andrade MartinsUniversidade Federal do Rio Grande do Norte - Programa de Pós-Graduação em Ciências Odontológicas - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0001-6245-0742
Isabelle de Lima MarquesUniversidade Federal do Rio Grande do Norte - Departamento de Morfologia - Natal (RN) - Brazil.ORCID http://orcid.org/0009-0005-7731-2867
Rafaela Alcindo SilvaUniversidade Federal do Rio Grande do Norte - Programa de Pós-Graduação em Ciências Odontológicas - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0002-5123-0741
Aurigena Antunes de AraújoUniversidade Federal do Rio Grande do Norte - Programa de Pós-Graduação em Ciências Odontológicas - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0001-9264-4695
Fabrício Gava MenezesUniversidade Federal do Rio Grande do Norte - Instituto de Química - Natal (RN) - Brazil.ORCID http://orcid.org/0000-0003-2153-1647

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBioactive molecules are relevant to fight cancer and associated conditions. Quinoxaline is a privileged N-heterocycle, notably as anticancer agents. Herein, we report the evaluation of the quinoxaline derivatives DEQX and OAQX as anticancer agents, as well as in function of their anti-inflammatory and analgesic activities.

methodsQuinoxalines were synthesized and tested as anticancer agents based on cell viability and Annexin V-FITC apoptosis. Anti-inflammatory activity was evaluated from mouse carrageenan peritonitis and levels of interleukin (IL)-1β and tumor necrosis factor (TNF)-alfa for enzyme-linked immunosorbent assay. Hot-plate and acetic acid-induced writing test were employed to investigate analgesia.

resultsBoth reduced the Ht-29 cell viability in a dependent-concentration manner (p < 0.001). Total apoptosis was detected for cells treated with 12.5 and 25 µg/mL of both the compounds for 24 and 48 h (all doses, p < 0.0001). DEQX (all doses, p < 0.01) and OAQX (all doses, p < 0.001) acted in leukocyte migration and decreased the IL-1β and TNF-β levels (p < 0.05). DEQX (all doses, p < 0.05) and OAQX (5mg/kg, p < 0.001) showed peripheral analgesic effect.

conclusionsIn-vitro and in-vivo results suggest that these quinoxalines are promising for application in pharmacological area due to their anticancer, anti-inflammatory, and peripheric analgesia.

Indexed as

AnalgesicsAnti-Inflammatory AgentsAntineoplastic AgentsApoptosisCell SurvivalQuinoxalinesAnimalsEnzyme-Linked Immunosorbent AssayHT29 CellsHumansInterleukin-1betaMaleMicePeritonitisTumor Necrosis Factor-alphaAnalgesicsAnti-Inflammatory AgentsAntineoplastic AgentsInterleukin-1betaQuinoxalinesTumor Necrosis Factor-alpha

Identifiers

PMID39109780
PMCPMC11299385

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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.