Evidence map›Paper›PMID 31117938›Full record

ArticleBMC genomics2019

Trans-chalcone activity against Trichophyton rubrum relies on an interplay between signaling pathways related to cell wall integrity and fatty acid metabolism.

Tamires Aparecida Bitencourt, Claudia Macedo, Matheus Eloy Franco, Marina Campos Rocha, Igor Sawasaki Moreli, Bruna Aline Micheloto Cantelli, Pablo Rodrigo Sanches, Rene Oliveira Beleboni, Iran Malavazi, Geraldo Aleixo Passos and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Biology · 2025
    Article
  3. Review
  4. Exploring the Therapeutic Potential ofInternational journal of molecular sciences · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Anti-Fungal Efficacy and Mechanisms of Flavonoids.Antibiotics (Basel, Switzerland) · 2020
    Review
  9. The Transcriptional Profile ofPathogens (Basel, Switzerland) · 2019
    Article
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

12 authors at 3 institutions in 1 country.

Tamires Aparecida BitencourtUnidade de Biotecnologia, Universidade de Ribeirão Preto, Av: Costábile Romano 2201, Ribeirão Preto, SP, 14096-900, Brazil.
Claudia MacedoDepartamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.
Matheus Eloy FrancoUnidade de Biotecnologia, Universidade de Ribeirão Preto, Av: Costábile Romano 2201, Ribeirão Preto, SP, 14096-900, Brazil.
Marina Campos RochaDepartamento de Genética e Evolução, Centro de Ciências Biológicas e da Saúde (CCBS), Universidade Federal de São Carlos, São Carlos, Brazil.
Igor Sawasaki MoreliUnidade de Biotecnologia, Universidade de Ribeirão Preto, Av: Costábile Romano 2201, Ribeirão Preto, SP, 14096-900, Brazil.
Bruna Aline Micheloto CantelliUnidade de Biotecnologia, Universidade de Ribeirão Preto, Av: Costábile Romano 2201, Ribeirão Preto, SP, 14096-900, Brazil.
Pablo Rodrigo SanchesDepartamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.
Rene Oliveira BeleboniUnidade de Biotecnologia, Universidade de Ribeirão Preto, Av: Costábile Romano 2201, Ribeirão Preto, SP, 14096-900, Brazil.
Iran MalavaziDepartamento de Genética e Evolução, Centro de Ciências Biológicas e da Saúde (CCBS), Universidade Federal de São Carlos, São Carlos, Brazil.
Geraldo Aleixo PassosDepartamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.
Mozart MarinsUnidade de Biotecnologia, Universidade de Ribeirão Preto, Av: Costábile Romano 2201, Ribeirão Preto, SP, 14096-900, Brazil.
Ana Lúcia FachinUnidade de Biotecnologia, Universidade de Ribeirão Preto, Av: Costábile Romano 2201, Ribeirão Preto, SP, 14096-900, Brazil. afachin@unaerp.br.
Universidade de Ribeirão Preto · BRUniversidade Federal de São Carlos · BRUniversidade de São Paulo · BR

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/02920-7 and 2015/23435-8Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/16881Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/22701-9
6 · The paper itself

Abstract

backgroundTrichophyton rubrum is the main etiological agent of skin and nail infections worldwide. Because of its keratinolytic activity and anthropophilic nature, infection models based on the addition of protein substrates have been employed to assess transcriptional profiles and to elucidate aspects related to host-pathogen interactions. Chalcones are widespread compounds with pronounced activity against dermatophytes. The toxicity of trans-chalcone towards T. rubrum is not fully understood but seems to rely on diverse cellular targets. Within this context, a better understanding of the mode of action of trans-chalcone may help identify new strategies of antifungal therapy and reveal new chemotherapeutic targets. This work aimed to assess the transcriptional profile of T. rubrum grown on different protein sources (keratin or elastin) to mimic natural infection sites and exposed to trans-chalcone in order to elucidate the mechanisms underlying the antifungal activity of trans-chalcone.

resultsOverall, the use of different protein sources caused only slight differences in the transcriptional profile of T. rubrum. The main differences were the modulation of proteases and lipases in gene categories when T. rubrum was grown on keratin and elastin, respectively. In addition, some genes encoding heat shock proteins were up-regulated during the growth of T. rubrum on keratin. The transcriptional profile of T. rubrum exposed to trans-chalcone included four main categories: fatty acid and lipid metabolism, overall stress response, cell wall integrity pathway, and alternative energy metabolism. Consistently, T. rubrum Mapk was strongly activated during the first hours of trans-chalcone exposure. Noteworthy, trans-chalcone inhibited genes involved in keratin degradation. The results also showed effects of trans-chalcone on fatty acid synthesis and metabolic pathways involved in acetyl-CoA supply.

conclusionOur results suggest that the mode of action of trans-chalcone is related to pronounced changes in fungal metabolism, including an imbalance between fatty acid synthesis and degradation that interferes with cell membrane and cell wall integrity. In addition, this compound exerts activity against important virulence factors. Taken together, trans-chalcone acts on targets related to dermatophyte physiology and the infection process.

Indexed as

Antifungal AgentsCell WallChalconeElastinFatty AcidsFungal ProteinsGene Expression ProfilingGene Expression Regulation, FungalHumansKeratinsSignal TransductionTineaTrichophytonVirulence FactorsAntifungal AgentsChalconeElastinFatty AcidsFungal ProteinsKeratinsVirulence FactorsChalconeCWIDermatophyteElastinKeratinTranscriptional profile

Identifiers

PMID31117938
PMCPMC6532161
OpenAlexW2947909391

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.