Evidence map›Paper›PMID 32187278›Full record

ArticleClinics (Sao Paulo, Brazil)2020

Apoptosis-related gene expression can predict the response of ovarian cancer cell lines to treatment with recombinant human TRAIL alone or combined with cisplatin.

Letícia da Conceição Braga, Nikole Gontijo Gonçales, Rafaela de Souza Furtado, Warne Pedro de Andrade, Luciana Maria Silva, Agnaldo Lopes da Silva Filho

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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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

6 authors at 3 institutions in 1 country.

Letícia da Conceição BragaServico de Biologia Celular da Diretoria de Pesquisa e Desenvolvimento, Fundacao Ezequiel Dias-Funed, Belo Horizonte, MG, BR.
Nikole Gontijo GonçalesServico de Biologia Celular da Diretoria de Pesquisa e Desenvolvimento, Fundacao Ezequiel Dias-Funed, Belo Horizonte, MG, BR.
Rafaela de Souza FurtadoDepartamento de Ginecologia e Obstetricia, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, MG, BR.
Warne Pedro de AndradeDepartamento de Ginecologia e Obstetricia, Faculdade de Ciencias Medicas e Biologicas de Botucatu, Universidade Estadual Paulista, Botucatu, SP, BR.
Luciana Maria SilvaServico de Biologia Celular da Diretoria de Pesquisa e Desenvolvimento, Fundacao Ezequiel Dias-Funed, Belo Horizonte, MG, BR.
Agnaldo Lopes da Silva FilhoDepartamento de Ginecologia e Obstetricia, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, MG, BR.
Ezequiel Dias Foundation · BRUniversidade Federal de Minas Gerais · BRUniversidade Estadual Paulista (Unesp) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objectives of this study were to determine the sensitivity of ovarian cancer (OC) cell lines (TOV-21G and SKOV-3) to cisplatin and to the recombinant human TRAIL (rhTRAIL), and to evaluate the expression profile of TNFRSF10B, TNFRSF10C, TP53TG5, MDM2, BAX, BCL-2 and CASPASE-8 genes and their participation in the resistance/susceptibility mechanism of these tumor cell lines.

methodsTo determine the IC50 values associated with Cisplatin and rhTRAIL, inhibition of cell growth was observed using MTT assays in two human OC cell lines (SKOV-3 and TOV-21G). The analysis of gene expression was performed using quantitative real-time polymerase chain reaction (qRT-PCR).

resultsBoth cell lines had different susceptibility profiles to the tested drugs. In the SKOV-3 cell line, the IC50 values for cisplatin and for rhTRAIL were 270.83 ug/mL and 196.5 ng/mL, respectively. The same concentrations were used for TOV-21G. Different gene expression profiles were observed in each tested cell line. CASPASE-8 and TNFRSF10B expression levels could predict the response of both the cell lines to rhTRAIL alone or the response to a combination of rhTRAIL and cisplatin. In addition, we observed a relationship between BCL-2 and BAX expression that may be helpful in estimating the proliferation rate of the OC cell lines.

conclusionSKOV-3 and TOV-21G respond differently to cisplatin and rhTRAIL exposure, and expression of CASPASE-8 and TNFRSF10B are good predictors of responses to these treatments.

Indexed as

Ovarian NeoplasmsAntineoplastic AgentsApoptosisCell Line, TumorCisplatinFemaleHumansAntineoplastic AgentsCisplatin

Identifiers

PMID32187278
PMCPMC7061320
OpenAlexW3011559775

What OpenQuestion holds

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LicenceCC BY
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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.