Evidence map›Paper›PMID 37047289›Full record

ArticleInternational journal of molecular sciences2023

Next Generation of Ovarian Cancer Detection Using Aptamers.

Rayane da Silva Abreu, Deborah Antunes, Aline Dos Santos Moreira, Fabio Passetti, Julia Badaró Mendonça, Natássia Silva de Araújo, Tayanne Felippe Sassaro, Anael Viana Pinto Alberto, Nina Carrossini, Priscila Valverde Fernandes and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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 15% 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, 12 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.

Rayane da Silva AbreuLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.ORCID 0000-0002-3470-1716
Deborah AntunesLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.ORCID 0000-0002-2927-0800
Aline Dos Santos MoreiraLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.ORCID 0000-0002-7979-6376
Fabio PassettiInstituto Carlos Chagas, Fundação Oswaldo Cruz (FIOCRUZ), Curitiba 81350-010, Brazil.ORCID 0000-0001-5672-7848
Julia Badaró MendonçaLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.ORCID 0000-0003-3673-2572
Natássia Silva de AraújoLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.ORCID 0000-0002-0790-0226
Tayanne Felippe SassaroLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.
Anael Viana Pinto AlbertoLaboratório de Tecnologia de Pós, Instituto Nacional de Tecnologia, Rio de Janeiro 20081-312, Brazil.
Nina CarrossiniDivisão de Patologia (DIPAT), Instituto Nacional do Câncer (INCA), Rio de Janeiro 20220-400, Brazil.
Priscila Valverde FernandesDivisão de Patologia (DIPAT), Instituto Nacional do Câncer (INCA), Rio de Janeiro 20220-400, Brazil.
Mayla Abrahim CostaLaboratório de Tecnologia Imunológica, Instituto de Tecnologia em Imunobiológicos, Bio-Manguinhos, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.
Ana Carolina Ramos GuimarãesLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.
Wim Maurits Sylvain DegraveLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.
Mariana Caldas WaghabiLaboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro 21040-900, Brazil.ORCID 0000-0002-1205-9507
Fundação Oswaldo Cruz · BRInstituto Nacional de Câncer - INCA · BRInstituto Nacional de Tecnologia · BR

Funding

INOVA Fiocruz VPPIS 001-FIO-18-58National Council for Scientific and Technological Development 457589/2013-2
6 · The paper itself

Abstract

Ovarian cancer is among the seven most common types of cancer in women, being the most fatal gynecological tumor, due to the difficulty of detection in early stages. Aptamers are important tools to improve tumor diagnosis through the recognition of specific molecules produced by tumors. Here, aptamers and their potential targets in ovarian cancer cells were analyzed by in silico approaches. Specific aptamers were selected by the Cell-SELEX method using Caov-3 and OvCar-3 cells. The five most frequent aptamers obtained from the last round of selection were computationally modeled. The potential targets for those aptamers in cells were proposed by analyzing proteomic data available for the Caov-3 and OvCar-3 cell lines. Overexpressed proteins for each cell were characterized as to their three-dimensional model, cell location, and electrostatic potential. As a result, four specific aptamers for ovarian tumors were selected: AptaC2, AptaC4, AptaO1, and AptaO2. Potential targets were identified for each aptamer through Molecular Docking, and the best complexes were AptaC2-FXYD3, AptaC4-ALPP, AptaO1-TSPAN15, and AptaO2-TSPAN15. In addition, AptaC2 and AptaO1 could detect different stages and subtypes of ovarian cancer tissue samples. The application of this technology makes it possible to propose new molecular biomarkers for the differential diagnosis of epithelial ovarian cancer.

Indexed as

Aptamers, NucleotideOvarian NeoplasmsApoptosisCell Line, TumorFemaleHumansMembrane ProteinsMolecular Docking SimulationNeoplasm ProteinsProteomicsSELEX Aptamer TechniqueAptamers, NucleotideFXYD3 protein, humanMembrane ProteinsNeoplasm Proteinsaptamerscomputational modelingovarian cancer

Identifiers

PMID37047289
PMCPMC10094455
OpenAlexW4361213415

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.