Evidence map›Paper›PMID 36014389›Full record

ArticleMolecules (Basel, Switzerland)2022

Pro-Apoptotic Antitumoral Effect of Novel Acridine-Core Naphthoquinone Compounds against Oral Squamous Cell Carcinoma.

Bruna Costa Zorzanelli, Gabriel Ouverney, Fernanda P Pauli, Anna Carolina Carvalho da Fonseca, Elan Cardozo Paes de Almeida, Danielle Gonçalves de Carvalho, Patricia Abrão Possik, Vitor Won-Held Rabelo, Paula Alvarez Abreu, Bruno Pontes and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 20 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

14 authors at 3 institutions in 1 country.

Bruna Costa ZorzanelliDepartamento de Química Orgânica, Instituto de Química, Campus do Valonguinho, Universidade Federal Fluminense, Niterói CEP 24020-141, Brazil.
Gabriel OuverneyDepartamento de Ciência Básica, Campus Universitário de Nova Friburgo, Universidade Federal Fluminense, Nova Friburgo CEP 28625-650, Brazil.
Fernanda P PauliDepartamento de Química Orgânica, Instituto de Química, Campus do Valonguinho, Universidade Federal Fluminense, Niterói CEP 24020-141, Brazil.
Anna Carolina Carvalho da FonsecaPrograma de Pós-graduação em Odontologia, Instituto de Saúde de Nova Friburgo, Universidade Federal Fluminense, Nova Friburgo CEP 28625-650, Brazil.ORCID 0000-0002-8366-3146
Elan Cardozo Paes de AlmeidaDepartamento de Ciência Básica, Campus Universitário de Nova Friburgo, Universidade Federal Fluminense, Nova Friburgo CEP 28625-650, Brazil.
Danielle Gonçalves de CarvalhoProgram of Immunology and Tumor Biology, Brazilian National Cancer Institute, Division of Experimental and Translational Research, Rio de Janeiro CEP 20231-050, Brazil.
Patricia Abrão PossikProgram of Immunology and Tumor Biology, Brazilian National Cancer Institute, Division of Experimental and Translational Research, Rio de Janeiro CEP 20231-050, Brazil.
Vitor Won-Held RabeloInstituto de Biodiversidade e Sustentabilidade, Universidade Federal do Rio de Janeiro, Macaé CEP 27965-045, Brazil.ORCID 0000-0001-5303-6814
Paula Alvarez AbreuInstituto de Biodiversidade e Sustentabilidade, Universidade Federal do Rio de Janeiro, Macaé CEP 27965-045, Brazil.ORCID 0000-0003-2204-3012
Bruno PontesInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro CEP 21941-902, Brazil.ORCID 0000-0002-0831-1204
Vitor Francisco FerreiraDepartamento de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Fluminense, Niterói CEP 24241-000, Brazil.ORCID 0000-0002-2166-766X
Luana da Silva Magalhães ForeziDepartamento de Química Orgânica, Instituto de Química, Campus do Valonguinho, Universidade Federal Fluminense, Niterói CEP 24020-141, Brazil.
Fernando de Carvalho da SilvaDepartamento de Química Orgânica, Instituto de Química, Campus do Valonguinho, Universidade Federal Fluminense, Niterói CEP 24020-141, Brazil.ORCID 0000-0002-2042-3778
Bruno Kaufmann RobbsDepartamento de Ciência Básica, Campus Universitário de Nova Friburgo, Universidade Federal Fluminense, Nova Friburgo CEP 28625-650, Brazil.
Universidade Federal Fluminense · BRUniversidade Federal do Rio de Janeiro · BRInstituto Nacional de Câncer - INCA · BR

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior Finance Code 001Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/010.001318/2019Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/010.002127/2019Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/10.002250/2019Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/200.870/2021Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/201.369/2021Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/202.787/2019Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/210.002/2020Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/210.068/2021Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/210.085/2022Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/211.343/2021National Council for Scientific and Technological Development 301873/2019-4National Council for Scientific and Technological Development 306011/2020-4National Council for Scientific and Technological Development 404587/2021-6
6 · The paper itself

Abstract

Oral squamous cell carcinoma (OSCC) is a global public health problem with high incidence and mortality. The chemotherapeutic agents used in the clinic, alone or in combination, usually lead to important side effects. Thus, the discovery and development of new antineoplastic drugs are essential to improve disease prognosis and reduce toxicity. In the present study, acridine-core naphthoquinone compounds were synthesized and evaluated for their antitumor activity in OSCC cells. The mechanism of action, pharmacokinetics, and toxicity parameters of the most promising compound was further analyzed using in silico, in vitro, and in vivo methods. Among the derivatives, compound

Indexed as

Antineoplastic AgentsCarcinoma, Squamous CellHead and Neck NeoplasmsMouth NeoplasmsNaphthoquinonesAcridinesAnimalsApoptosisCell Line, TumorCell ProliferationMolecular Docking SimulationSquamous Cell Carcinoma of Head and NeckAcridinesAntineoplastic AgentsNaphthoquinonesacridinesnaphthoquinonesoral squamous cell carcinomapyruvate kinase m2selectivity

Identifiers

PMID36014389
PMCPMC9415509
OpenAlexW4291891419

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.