Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes

Detalhes bibliográficos
Autor(a) principal: Serpeloni, J. M. [UNESP]
Data de Publicação: 2020
Outros Autores: Specian, A. F.L., Ribeiro, D. L., Benício, L. M., Nunes, H. L., Franchi, L. P., Rocha, C. Q., Vilegas, W. [UNESP], Varanda, E. A. [UNESP], Cólus, I. M.S. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1177/0960327119888261
http://hdl.handle.net/11449/199669
Resumo: Fridericia platyphylla (Cham.) L.G. Lohmann (FP) has cytotoxic, anti-inflammatory, and analgesic properties. We aimed to characterize the cytotoxic and antiproliferative effects of FP extract on normal (GAS) and tumor-derived (ACP02 and HepG2) cell lines. The effective concentrations (EC50s) by tetrazolium bromide assay (MTT) were 56.16, 43.68, and 42.57 µg mL−1 and 69.38, 41.73, and 52.39 µg mL−1 by neutral red assay for GAS, ACP02, and HepG2 cells, respectively. The extract decreased nuclear division indices, which was not reflected in cell proliferation curves. Flow cytometric analyses showed that even 30 µg mL−1 extract (shown to be noncytotoxic by MTT assay) increased the sub-G1 population, indicating cell death due to apoptosis and necrosis. A cytokinesis-block micronucleus cytome assay showed that 30 µg mL−1 of the extract increased the frequency of nuclear buds in tumor cells. Real-time quantitative polymerase chain reaction showed CCND1 upregulation in doxorubicin-treated GAS cells and BCL-XL, BIRC5, and MET downregulation in 5 or 30 µg mL−1 in FP extract-treated ACP02 cells. In conclusion, FP extract modulated apoptosis- and cell cycle-related genes and presented selective cytotoxicity toward tumor cells that deserves further investigation by testing other cell types. Our results demonstrated that even medicinal plants exert adverse effects depending on the extract concentrations used and tissues investigated.
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spelling Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genesAntiproliferativeapoptosisFridericia platyphyllagastric cellsNBUDsFridericia platyphylla (Cham.) L.G. Lohmann (FP) has cytotoxic, anti-inflammatory, and analgesic properties. We aimed to characterize the cytotoxic and antiproliferative effects of FP extract on normal (GAS) and tumor-derived (ACP02 and HepG2) cell lines. The effective concentrations (EC50s) by tetrazolium bromide assay (MTT) were 56.16, 43.68, and 42.57 µg mL−1 and 69.38, 41.73, and 52.39 µg mL−1 by neutral red assay for GAS, ACP02, and HepG2 cells, respectively. The extract decreased nuclear division indices, which was not reflected in cell proliferation curves. Flow cytometric analyses showed that even 30 µg mL−1 extract (shown to be noncytotoxic by MTT assay) increased the sub-G1 population, indicating cell death due to apoptosis and necrosis. A cytokinesis-block micronucleus cytome assay showed that 30 µg mL−1 of the extract increased the frequency of nuclear buds in tumor cells. Real-time quantitative polymerase chain reaction showed CCND1 upregulation in doxorubicin-treated GAS cells and BCL-XL, BIRC5, and MET downregulation in 5 or 30 µg mL−1 in FP extract-treated ACP02 cells. In conclusion, FP extract modulated apoptosis- and cell cycle-related genes and presented selective cytotoxicity toward tumor cells that deserves further investigation by testing other cell types. Our results demonstrated that even medicinal plants exert adverse effects depending on the extract concentrations used and tissues investigated.Fundação de Amparo à Pesquisa e ao Desenvolvimento Científico e Tecnológico do MaranhãoLaboratory of Mutagenesis Department of Biological Sciences Faculty of Pharmaceutical Sciences São Paulo State University (UNESP)Laboratory of Mutagenesis and Oncogenetics Department of General Biology Center of Biological Sciences State University of Londrina (UEL)Laboratory of Cytogenetics and Mutagenesis Department of Biology Faculty of Philosophy Sciences and Letters of Ribeirão Preto (FFCLRP)Laboratory of Advanced Studies in Phytomedicines Department of Chemistry Federal University of Maranhão (UFMA)Campus Litoral Paulista São Paulo State University (UNESP)Laboratory of Mutagenesis Department of Biological Sciences Faculty of Pharmaceutical Sciences São Paulo State University (UNESP)Campus Litoral Paulista São Paulo State University (UNESP)Fundação de Amparo à Pesquisa e ao Desenvolvimento Científico e Tecnológico do Maranhão: 00863/16Universidade Estadual Paulista (Unesp)Universidade Estadual de Londrina (UEL)Sciences and Letters of Ribeirão Preto (FFCLRP)Federal University of Maranhão (UFMA)Serpeloni, J. M. [UNESP]Specian, A. F.L.Ribeiro, D. L.Benício, L. M.Nunes, H. L.Franchi, L. P.Rocha, C. Q.Vilegas, W. [UNESP]Varanda, E. A. [UNESP]Cólus, I. M.S. [UNESP]2020-12-12T01:46:10Z2020-12-12T01:46:10Z2020-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article338-354http://dx.doi.org/10.1177/0960327119888261Human and Experimental Toxicology, v. 39, n. 3, p. 338-354, 2020.1477-09030960-3271http://hdl.handle.net/11449/19966910.1177/09603271198882612-s2.0-85075170956Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengHuman and Experimental Toxicologyinfo:eu-repo/semantics/openAccess2024-06-24T13:08:01Zoai:repositorio.unesp.br:11449/199669Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:28:17.486300Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
title Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
spellingShingle Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
Serpeloni, J. M. [UNESP]
Antiproliferative
apoptosis
Fridericia platyphylla
gastric cells
NBUDs
title_short Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
title_full Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
title_fullStr Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
title_full_unstemmed Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
title_sort Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes
author Serpeloni, J. M. [UNESP]
author_facet Serpeloni, J. M. [UNESP]
Specian, A. F.L.
Ribeiro, D. L.
Benício, L. M.
Nunes, H. L.
Franchi, L. P.
Rocha, C. Q.
Vilegas, W. [UNESP]
Varanda, E. A. [UNESP]
Cólus, I. M.S. [UNESP]
author_role author
author2 Specian, A. F.L.
Ribeiro, D. L.
Benício, L. M.
Nunes, H. L.
Franchi, L. P.
Rocha, C. Q.
Vilegas, W. [UNESP]
Varanda, E. A. [UNESP]
Cólus, I. M.S. [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Estadual de Londrina (UEL)
Sciences and Letters of Ribeirão Preto (FFCLRP)
Federal University of Maranhão (UFMA)
dc.contributor.author.fl_str_mv Serpeloni, J. M. [UNESP]
Specian, A. F.L.
Ribeiro, D. L.
Benício, L. M.
Nunes, H. L.
Franchi, L. P.
Rocha, C. Q.
Vilegas, W. [UNESP]
Varanda, E. A. [UNESP]
Cólus, I. M.S. [UNESP]
dc.subject.por.fl_str_mv Antiproliferative
apoptosis
Fridericia platyphylla
gastric cells
NBUDs
topic Antiproliferative
apoptosis
Fridericia platyphylla
gastric cells
NBUDs
description Fridericia platyphylla (Cham.) L.G. Lohmann (FP) has cytotoxic, anti-inflammatory, and analgesic properties. We aimed to characterize the cytotoxic and antiproliferative effects of FP extract on normal (GAS) and tumor-derived (ACP02 and HepG2) cell lines. The effective concentrations (EC50s) by tetrazolium bromide assay (MTT) were 56.16, 43.68, and 42.57 µg mL−1 and 69.38, 41.73, and 52.39 µg mL−1 by neutral red assay for GAS, ACP02, and HepG2 cells, respectively. The extract decreased nuclear division indices, which was not reflected in cell proliferation curves. Flow cytometric analyses showed that even 30 µg mL−1 extract (shown to be noncytotoxic by MTT assay) increased the sub-G1 population, indicating cell death due to apoptosis and necrosis. A cytokinesis-block micronucleus cytome assay showed that 30 µg mL−1 of the extract increased the frequency of nuclear buds in tumor cells. Real-time quantitative polymerase chain reaction showed CCND1 upregulation in doxorubicin-treated GAS cells and BCL-XL, BIRC5, and MET downregulation in 5 or 30 µg mL−1 in FP extract-treated ACP02 cells. In conclusion, FP extract modulated apoptosis- and cell cycle-related genes and presented selective cytotoxicity toward tumor cells that deserves further investigation by testing other cell types. Our results demonstrated that even medicinal plants exert adverse effects depending on the extract concentrations used and tissues investigated.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T01:46:10Z
2020-12-12T01:46:10Z
2020-03-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1177/0960327119888261
Human and Experimental Toxicology, v. 39, n. 3, p. 338-354, 2020.
1477-0903
0960-3271
http://hdl.handle.net/11449/199669
10.1177/0960327119888261
2-s2.0-85075170956
url http://dx.doi.org/10.1177/0960327119888261
http://hdl.handle.net/11449/199669
identifier_str_mv Human and Experimental Toxicology, v. 39, n. 3, p. 338-354, 2020.
1477-0903
0960-3271
10.1177/0960327119888261
2-s2.0-85075170956
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Human and Experimental Toxicology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 338-354
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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