Evidence map›Paper›PMID 42848143›Full record

ArticleNeurochemical research2026

Characterization and Selective Antiglioma Activity of a Standardized Hydroalcoholic Extract from Yellow Psidium cattleianum Fruits.

Francieli da Silva Dos Santos, Juliane Torchelsen Saraiva, Giulia Bueno de Oliveira da Silva, Natália Pontes Bona, William Sanabria Simões, Jessica Fernanda Hoffmann, Fabio Clasen Chaves, Marcia Vizzotto, Gabriela Nogueira Debom, Elizandra Braganhol and 4 more

Abstract read
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In one paragraph

Article in Neurochemical research, 2026. 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

14 authors.

Francieli da Silva Dos SantosPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0009-0002-9887-8825
Juliane Torchelsen SaraivaPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0009-0008-7124-5183
Giulia Bueno de Oliveira da SilvaPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0009-0006-9221-9406
Natália Pontes BonaPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0000-0001-5944-1968
William Sanabria SimõesPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0009-0000-5291-3336
Jessica Fernanda HoffmannInstituto Tecnológico em Alimentos para a Saúde, Universidade do Vale do Rio dos Sinos, São Leopoldo, 93022-750, Brazil.ORCID http://orcid.org/0000-0002-9185-3820
Fabio Clasen ChavesPrograma de Pós-Graduação em Ciência e Tecnologia de Alimentos, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0000-0002-5773-0800
Marcia VizzottoEmpresa Brasileira de Pesquisa Agropecuária Clima Temperado, Pelotas, 96010-971, RS, Brazil.ORCID http://orcid.org/0000-0002-8071-4980
Gabriela Nogueira DebomPrograma de Pós-Graduação em Biociências, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, 90050-170, RS, Brazil.ORCID http://orcid.org/0000-0002-3921-479X
Elizandra BraganholPrograma de Pós-Graduação em Biociências, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, 90050-170, RS, Brazil.ORCID http://orcid.org/0000-0002-9105-3858
Mayara Sandrielly Soares de AguiarPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil. mspereirasoares@gmail.com.ORCID http://orcid.org/0000-0002-2181-3591
Roselia Maria SpanevelloPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0000-0002-5117-2000
Nathalia Stark PedraPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0000-0001-8662-7661
Francieli Moro StefanelloPrograma de Pós-Graduação em Bioquímica e Bioprospecção, Universidade Federal de Pelotas, Capão do Leão, 96160-000, RS, Brazil.ORCID http://orcid.org/0000-0001-5945-3723

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is an aggressive and prevalent malignant brain tumor and remains a major public health challenge. Prognosis is poor, with median survival of 14-18 months and fewer than 7% of patients surviving beyond five years, reinforcing the need for new therapeutic strategies. Natural products are a traditional source of bioactive substances, and fruits are rich in phenolic constituents with potential anticancer activity. Psidium cattleianum, a Myrtaceae species native to South America, produces red and yellow fruits rich in vitamin C and phenolics, although biological data on the yellow variety are scarce. Preliminary evidence suggests anti-inflammatory, antioxidant, and antineoplastic activities, but studies in glioma models are limited. This study characterized the phenolic profile and evaluated the activity of a hydroalcoholic extract from yellow Psidium cattleianum (YPC) fruits in GBM and non-tumor cells. LC-MS analysis identified ellagic acid, catechin, and gallic acid as major constituents. Biological activity was assessed in glioma cell lines (C6 and U87MG), primary astrocytes, and fibroblast lines (L929 and MRC5). Cells were treated with extract concentrations ranging from 125 to 2000 µg/mL for 2 to 72 h. The extract significantly reduced proliferation, viability, colony formation and reactive oxygen species levels in glioma cells, while increasing glutathione peroxidase activity. In C6 cells, it also inhibited migration. Astrocytes and fibroblasts remained unaffected by cytotoxicity under the evaluated conditions. These findings demonstrate a selective antineoplastic potential of the YPC extract in glioma cells and support its relevance for further investigation in GBM treatment.

Indexed as

Antineoplastic Agents, PhytogenicBrain NeoplasmsFruitGliomaPlant ExtractsPsidiumAnimalsCell Line, TumorCell ProliferationCell SurvivalHumansMiceRatsReactive Oxygen SpeciesAntineoplastic Agents, PhytogenicPlant ExtractsReactive Oxygen SpeciesApoptosisCancerCytotoxicityEllagic acidGlioblastomaNatural products

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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.