PLA2-MjTX-II from Bothrops moojeni snake venom exhibits antimetastatic and antiangiogenic effects on human lung cancer cells
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DC Field | Value | Language |
---|---|---|
dc.contributor | Lab. Imunopatologia | pt_BR |
dc.contributor.author | Santos, Luísa Carregosa | pt_BR |
dc.contributor.author | Oliveira, Vinícius Queiroz | pt_BR |
dc.contributor.author | Teixeira, Samuel Cota | pt_BR |
dc.contributor.author | Clissa, Patricia Bianca | pt_BR |
dc.date.accessioned | 2024-06-07T18:08:11Z | - |
dc.date.available | 2024-06-07T18:08:11Z | - |
dc.date.issued | 2024 | pt_BR |
dc.identifier.uri | https://repositorio.butantan.gov.br/handle/butantan/5382 | - |
dc.description.abstract | Phospholipases A2 (PLA2s) from snake venom possess antitumor and antiangiogenic properties. In this study, we evaluated the antimetastatic and antiangiogenic effects of MjTX-II, a Lys49 PLA2 isolated from Bothrops moojeni venom, on lung cancer and endothelial cells. Using in vitro and ex vivo approaches, we demonstrated that MjTX-II reduced cell proliferation and inhibited fundamental processes for lung cancer cells (A549) growth and metastasis, such as adhesion, migration, invasion, and actin cytoskeleton decrease, without significantly interfering with non-tumorigenic lung cells (BEAS-2B). Furthermore, MjTX-II caused cell cycle alterations, increased reactive oxygen species production, modulated the expression of pro- and antiangiogenic genes, and decreased vascular endothelial growth factor (VEGF) expression in HUVECs. Finally, MjTX-II inhibited ex vivo angiogenesis processes in an aortic ring model. Therefore, we conclude that MjTX-II exhibits antimetastatic and antiangiogenic effects in vitro and ex vivo and represents a molecule that hold promise as a pharmacological model for antitumor therapy. | pt_BR |
dc.description.sponsorship | (FAPEMIG) Fundação de Amparo à Pesquisa do Estado de Minas Gerais | pt_BR |
dc.description.sponsorship | (CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico | pt_BR |
dc.description.sponsorship | (CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior | pt_BR |
dc.format.extent | 107742 | pt_BR |
dc.language.iso | English | pt_BR |
dc.relation.ispartof | Toxicon | pt_BR |
dc.rights | Restricted access | pt_BR |
dc.title | PLA2-MjTX-II from Bothrops moojeni snake venom exhibits antimetastatic and antiangiogenic effects on human lung cancer cells | pt_BR |
dc.type | Article | pt_BR |
dc.identifier.doi | 10.1016/j.toxicon.2024.107742 | pt_BR |
dc.identifier.url | https://doi.org/10.1016/j.toxicon.2024.107742 | pt_BR |
dc.contributor.external | (UFBA) Universidade Federal da Bahia | pt_BR |
dc.contributor.external | (UFU) Universidade Federal de Uberlândia | pt_BR |
dc.contributor.external | (UEL) Universidade Estadual de Londrina | pt_BR |
dc.contributor.external | (USP) Universidade de São Paulo | pt_BR |
dc.identifier.citationvolume | 243 | pt_BR |
dc.subject.keyword | MjTX-II | pt_BR |
dc.subject.keyword | lung cancer | pt_BR |
dc.subject.keyword | angiogenic | pt_BR |
dc.subject.keyword | Phospholipases A2 | pt_BR |
dc.subject.keyword | snake venom | pt_BR |
dc.relation.ispartofabbreviated | Toxicon | pt_BR |
dc.identifier.citationabnt | v. 243, 107742, mai. 2024 | pt_BR |
dc.identifier.citationvancouver | 2024 May; 243:107742 | pt_BR |
dc.contributor.butantan | Clissa, Patricia Bianca|:Pesquisador|:Lab. Imunopatologia | pt_BR |
dc.sponsorship.butantan | (FAPEMIG) Fundação de Amparo à Pesquisa do Estado de Minas Gerais¦¦APQ-01401-17 | pt_BR |
dc.sponsorship.butantan | (FAPEMIG) Fundação de Amparo à Pesquisa do Estado de Minas Gerais¦¦465669/2014-0 | pt_BR |
dc.sponsorship.butantan | (CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior¦¦001 | pt_BR |
dc.identifier.bvscc | BR78.1 | pt_BR |
dc.identifier.bvsdb | IBProd | pt_BR |
dc.description.dbindexed | Yes | pt_BR |
item.fulltext | Sem Texto completo | - |
item.languageiso639-1 | English | - |
item.openairetype | Article | - |
item.grantfulltext | none | - |
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crisitem.author.orcid | 000-0002-4213-4053 | - |
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