Evidence map›Paper›PMID 35297003›Full record

ArticlePharmacological reports : PR2022

Apoptotic and antioxidant effects in HCT-116 colorectal carcinoma cells by a spiro-acridine compound, AMTAC-06.

Sâmia Sousa Duarte, Daiana Karla Frade Silva, Thaís Mangeon Honorato Lisboa, Rawny Galdino Gouveia, Camyla Caroliny Neves de Andrade, Valgrícia Matias de Sousa, Rafael Carlos Ferreira, Ricardo Olimpio de Moura, Joilly Nilce Santana Gomes, Patricia Mirella da Silva and 5 more

Abstract read
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Article in Pharmacological reports : PR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

15 authors at 2 institutions in 1 country.

Sâmia Sousa DuartePostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Daiana Karla Frade SilvaPostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Thaís Mangeon Honorato LisboaPostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Rawny Galdino GouveiaPostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Camyla Caroliny Neves de AndradePostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Valgrícia Matias de SousaPostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Rafael Carlos FerreiraPostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Ricardo Olimpio de MouraDrug Development and Synthesis Laboratory, Department of Pharmacy, State University of Paraíba, João Pessoa, Paraíba, Brazil.
Joilly Nilce Santana GomesDrug Development and Synthesis Laboratory, Department of Pharmacy, State University of Paraíba, João Pessoa, Paraíba, Brazil.
Patricia Mirella da SilvaInvertebrate Immunology and Pathology Laboratory, Department of Molecular Biology, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Fátima de Lourdes Assunção Araújo de AzevedoCardiovascular Pharmacology Laboratory, Postgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Tatjana S L KeesenImmunology of Infectious Diseases Laboratory, Biotechnology Center, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Juan Carlos Ramos GonçalvesDepartment of Pharmaceutical Sciences, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Leônia Maria BatistaPostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Marianna Vieira SobralPostgraduation Program in Bioactive Natural and Synthetic Products, Federal University of Paraíba, João Pessoa, Paraíba, Brazil. mariannavbs@ltf.ufpb.br.ORCID http://orcid.org/0000-0002-7740-034X
Universidade Federal da Paraíba · BRUniversidade Estadual da Paraíba · BR

Funding

CAPES Finance Code 001FAPESQPB Finance Code 013/2018PROPESQ, Universidade Federal da Paraiba PIG13275-2020
6 · The paper itself

Abstract

backgroundAcridine compounds have been described as promising anticancer agents. Previous studies showed that (E)-1'-((4-chlorobenzylidene)amino)-5'-oxo-1',5'-dihydro-10H-spiro[acridine-9,2'-pyrrole]-4'-carbonitrile (AMTAC-06), a spiro-acridine compound, has antitumor activity on Ehrlich tumor and low toxicity. Herein, we investigated its antitumor effect against human cells in vitro.

methodsMTT assay was used to assess cytotoxicity of AMTAC-06 (3.125-200 µM) against tumor and non-tumor cells, and the half-maximal inhibitory concentration (IC

resultsAMTAC-06 showed higher cytotoxicity against colorectal carcinoma HCT-116 cells (IC

conclusionsAMTAC-06 presents anticancer activity against HCT-116 cells by regulating the cell cycle, inducing apoptosis and an antioxidant action.

Indexed as

Antineoplastic AgentsColorectal NeoplasmsSpiro CompoundsAcridinesAntioxidantsApoptosisCell Line, TumorCell ProliferationHCT116 CellsHumansLeukocytes, MononuclearReactive Oxygen SpeciesAcridinesAntineoplastic AgentsAntioxidantsReactive Oxygen SpeciesSpiro CompoundsAntioxidant actionAntitumor activityApoptosisCell cycleColorectal cancerSpiro-acridine

Identifiers

PMID35297003
OpenAlexW4220703955

What OpenQuestion holds

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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.