Evidence map›Paper›PMID 28965321›Full record

ArticleMolecular neurobiology2018

Pro-necrotic Activity of Cationic Mastoparan Peptides in Human Glioblastoma Multiforme Cells Via Membranolytic Action.

Annielle Mendes Brito da Silva, Laíz Costa Silva-Gonçalves, Fernando Augusto Oliveira, Manoel Arcisio-Miranda

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 48 citations in OpenAlex.

  1. Artificial intelligence catalyzes antimicrobial peptide design.Synthetic and systems biotechnology · 2027
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  6. Anti-Tumor Effects ofToxins · 2024
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  18. The Antimicrobial Peptide MPX Can KillFrontiers in veterinary science · 2022
    Article
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

Annielle Mendes Brito da SilvaLaboratório de Neurobiologia Estrutural e Funcional (LaNEF), Departamento de Biofísica, Escola Paulista de Medicina, Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brazil.
Laíz Costa Silva-GonçalvesLaboratório de Neurobiologia Estrutural e Funcional (LaNEF), Departamento de Biofísica, Escola Paulista de Medicina, Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brazil.
Fernando Augusto OliveiraLaboratório de Neurobiologia Celular e Molecular (LaNeC), Centro de Matemática, Computação e Cognição, Universidade Federal do ABC (UFABC), São Bernardo do Campo, São Paulo, SP, Brazil.
Manoel Arcisio-MirandaLaboratório de Neurobiologia Estrutural e Funcional (LaNEF), Departamento de Biofísica, Escola Paulista de Medicina, Universidade Federal de São Paulo (Unifesp), São Paulo, SP, Brazil. arcisio.miranda@unifesp.br.ORCID http://orcid.org/0000-0002-1086-086X
Universidade Federal de São Paulo · BRUniversidade Federal do ABC · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 142066/2014-1Conselho Nacional de Desenvolvimento Científico e Tecnológico 477780/2010-5Fundação de Amparo à Pesquisa do Estado de São Paulo 2009/53840-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/02065-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/50336-2Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/13368-4
6 · The paper itself

Abstract

Glioblastoma multiforme is the most common and lethal malignant brain tumor. Because of its complexity and heterogeneity, this tumor has become resistant to conventional therapies and the available treatment produces multiple side effects. Here, using multiple experimental approaches, we demonstrate that three mastoparan peptides-Polybia-MP1, Mastoparan X, and HR1-from solitary wasp venom exhibit potent anticancer activity toward human glioblastoma multiforme cells. Importantly, the antiglioblastoma action of mastoparan peptides occurs by membranolytic activity, leading to necrosis. Our data also suggest a direct relation between mastoparan membranolytic potency and the presence of negatively charged phospholipids like phosphatidylserine. Collectively, these data may warrant additional studies for mastoparan peptides as new agents for the treatment of glioblastoma multiforme brain tumor.

Indexed as

Amino Acid SequenceCalciumCationsCell Line, TumorCell MembraneCell NucleusCell ShapeCell SurvivalGlioblastomaHumansIntercellular Signaling Peptides and ProteinsMembrane Potential, MitochondrialNecrosisPeptidesProtein Structure, SecondaryWasp VenomsCalciumCationsIntercellular Signaling Peptides and ProteinsmastoparanPeptidesWasp VenomsCationic peptideGlioblastomaMastoparanNecrosisPhosphatidylserine

Identifiers

PMID28965321
OpenAlexW2759912632

What OpenQuestion holds

Textmetadata
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.