Evidence map›Paper›PMID 37353536›Full record

ArticleScientific reports2023

The potential of phenothiazinium dyes as cytotoxicity markers in cisplatin-treated cells.

Luiz Miguel Pereira, Gisele Bulhões Portapilla, Guilherme Thomaz Pereira Brancini, Bruna Possato, Cássia Mariana Bronzon da Costa, Péricles Gama Abreu-Filho, Mark Wainwright, Ana Patrícia Yatsuda, Gilberto Úbida Leite Braga

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Luiz Miguel PereiraFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil.
Gisele Bulhões PortapillaFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil.
Guilherme Thomaz Pereira BranciniFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil.
Bruna PossatoFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil.
Cássia Mariana Bronzon da CostaFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil.
Péricles Gama Abreu-FilhoFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil.
Mark WainwrightDepartment of Biology, Edge Hill University, Ormskirk, L39 4QP, UK.
Ana Patrícia YatsudaFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil. ayatsuda@fcfrp.usp.br.
Gilberto Úbida Leite BragaFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Av do Café, sn/n, Ribeirão Preto, SP, 14040-903, Brazil. gbraga@fcfrp.usp.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Assessing the in vitro toxicity of compounds on cell cultures is an important step during the screening of candidate molecules for diverse applications. Among the strategies employed to determine cytotoxicity, MTT, neutral red, and resazurin are commonly used. Methylene blue (MB), a phenothiazinium salt, has several uses, such as dye, redox indicator, and even as treatment for human disease and health conditions, such as malaria and methemoglobinemia. However, MB has only been sparsely used as a cellular toxicity indicator. As a viability indicator, MB is mostly applied to fixed cultures at high concentrations, especially when compared to MTT or neutral red. Here we show that MB and its related compounds new methylene blue (NMB), toluidine blue O (TBO), and dimethylmethylene blue (DMMB) can be used as cytotoxicity indicators in live (non-fixed) cells treated for 72 h with DMSO and cisplatin. We compared dye uptake between phenothiazinium dyes and neutral red by analyzing supernatant and cell content via visible spectra scanning and microscopy. All dyes showed a similar ability to assess cell toxicity compared to either MTT or neutral red. Our method represents a cost-effective alternative to in vitro cytotoxicity assays using cisplatin or DMSO, indicating the potential of phenothiazinium dyes for the screening of candidate drugs and other applications.

Indexed as

Coloring AgentsPhenothiazinesCisplatinDimethyl SulfoxideHumansMethylene BlueNeutral RedCisplatinColoring AgentsDimethyl SulfoxideMethylene BlueNeutral RedPhenothiazines

Identifiers

PMID37353536
PMCPMC10290130

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Registered trials

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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.