Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais
Autor(a) principal: | |
---|---|
Data de Publicação: | 2018 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6433179 https://repositorio.unifesp.br/handle/11600/53054 |
Resumo: | Introduction: The bone marrow microenvironment is a milieu complex of various types of stromal and hematopoietic cells involved in the selfrenewal and differentiation of stem cells and hematopoietic progenitors (HSPC). Several soluble and membranebound factors produced by endothelial cells (EC) and perivascular stroma are crucial signals to maintain quiescence and facilitate the return to homeostasis after myeloablative chemotherapy. In addition, several studies have shown a relationship between HSPCs and ECs, pointing to hemangioblastic activity in HSPCs, both in the generation of cells and blood vessels. Considering the relationships between HSPCs and CSs in the bone marrow, it is possible to implicate CDEs in the establishment and progression of malignant HSPCs such as acute and chronic myeloid leukemias. In fact, in leukemias, studies have shown that angiogenesis also contributes to its pathogenesis, with an increase in bone marrow vascularization, associated with elevated levels of angiogenic factors. Thus, therapeutic strategies that aim to inhibit the angiogenic process may aid in the treatment of leukemia. OBJECTIVE: The objective of this study was to investigate the antiangiogenic effect of violacein on rabbit aortic endothelial cell (RAEC) and leukemic cells from the K562 and Lucena1 (K562 with MDR1 phenotype) lines. Results: It was observed that violacein, at concentrations lower than its IC 50, is able to inhibit capillary tube formation, proliferation, migration and invasion of ECs, with IC50 of RAEC cells (5.0 μM) higher than IC 50 Of the leukemic cells (3.5 μM). When RAEC cells were cocultured with leukemia cells in direct contact, in the presence of inserts or with the conditioned medium of the leukemic cells, an increase in proliferation, capillary formation, migration and invasion of RAEC cells was observed. In addition, the increase in these parameters was higher in cocultures with the Lucena1 lineage. In contrast, pretreatment of leukemic cells with violacein significantly reduced these effects, with inhibition of the VEGFR2 / PI3K / AKT and VEGFR2 / Src / MAPK pathways in the studied strains (ECs and leukemias). Taken together, the results show the importance of soluble factors in the modulation of the events associated with the angiogenic process and demonstrate the antiangiogenic potential of violacein with action in important ways of regulating angiogenesis and cell proliferation. |
id |
UFSP_92ffc87e16e3945d7c5cf4e9d923a224 |
---|---|
oai_identifier_str |
oai:repositorio.unifesp.br/:11600/53054 |
network_acronym_str |
UFSP |
network_name_str |
Repositório Institucional da UNIFESP |
repository_id_str |
3465 |
spelling |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliaisInvestigation of antitumor and antiangiogênica activity of violacein in coculture of leucemic cells and endothelial cellsL LeukemiaCancerLLeucemiaAngiogeneseCâncerViolaceínaViolaceinAngiogenesisIntroduction: The bone marrow microenvironment is a milieu complex of various types of stromal and hematopoietic cells involved in the selfrenewal and differentiation of stem cells and hematopoietic progenitors (HSPC). Several soluble and membranebound factors produced by endothelial cells (EC) and perivascular stroma are crucial signals to maintain quiescence and facilitate the return to homeostasis after myeloablative chemotherapy. In addition, several studies have shown a relationship between HSPCs and ECs, pointing to hemangioblastic activity in HSPCs, both in the generation of cells and blood vessels. Considering the relationships between HSPCs and CSs in the bone marrow, it is possible to implicate CDEs in the establishment and progression of malignant HSPCs such as acute and chronic myeloid leukemias. In fact, in leukemias, studies have shown that angiogenesis also contributes to its pathogenesis, with an increase in bone marrow vascularization, associated with elevated levels of angiogenic factors. Thus, therapeutic strategies that aim to inhibit the angiogenic process may aid in the treatment of leukemia. OBJECTIVE: The objective of this study was to investigate the antiangiogenic effect of violacein on rabbit aortic endothelial cell (RAEC) and leukemic cells from the K562 and Lucena1 (K562 with MDR1 phenotype) lines. Results: It was observed that violacein, at concentrations lower than its IC 50, is able to inhibit capillary tube formation, proliferation, migration and invasion of ECs, with IC50 of RAEC cells (5.0 μM) higher than IC 50 Of the leukemic cells (3.5 μM). When RAEC cells were cocultured with leukemia cells in direct contact, in the presence of inserts or with the conditioned medium of the leukemic cells, an increase in proliferation, capillary formation, migration and invasion of RAEC cells was observed. In addition, the increase in these parameters was higher in cocultures with the Lucena1 lineage. In contrast, pretreatment of leukemic cells with violacein significantly reduced these effects, with inhibition of the VEGFR2 / PI3K / AKT and VEGFR2 / Src / MAPK pathways in the studied strains (ECs and leukemias). Taken together, the results show the importance of soluble factors in the modulation of the events associated with the angiogenic process and demonstrate the antiangiogenic potential of violacein with action in important ways of regulating angiogenesis and cell proliferation.Introdução: O microambiente da medula óssea é um complexo milieu de diversos tipos de células estromais e hematopoéticas envolvidas na autorenovação e diferenciação das célulastronco e progenitoras hematopoéticas (HSPC). Vários fatores solúveis e ligados à membrana produzidos pelas células endoteliais (EC) e pelo estroma perivascular constituem sinais cruciais para manter a quiescência e facilitar o retorno à homeostase após quimioterapia mieloablativa. Além disso, vários trabalhos demonstram uma relação entre HSPCs e ECs, apontando atividade hemangioblástica às HSPCs, tanto na geração das células como dos vasos sanguíneos. Considerando as relações entre HSPCs e ECs na medula óssea, é possível implicar as ECs no estabelecimento e progressão de HSPCs malignas como as leucemias mieloides aguda e crônica. De fato, nas leucemias, estudos demonstram que a angiogênese também contribui para sua patogênese, havendo um aumento na vascularização da medula óssea, associado a níveis elevados de fatores angiogênicos. Desta forma, as estratégias terapêuticas que visam inibir o processo angiogênico podem auxiliar o tratamento da leucemia. Objetivo: este estudo tem como objetivo investigar o efeito antiangiogênico da violaceína em sistemas de cocultura de células endoteliais de aorta de coelho (RAEC) e células leucêmicas das linhagens K562 e Lucena1 (K562 com fenótipo MDR1). Resultados: Observouse que a violaceína, em concentrações inferiores ao seu IC50, é capaz de inibir a formação de tubo capilar, a proliferação, migração e invasão de ECs, sendo o IC50 das células RAEC (5,0 μM) superior ao IC50 das células leucêmicas (3,5 μM). Quando as células RAEC foram cocultivadas com células de leucemia em contato direto, na presença de insertos ou com o meio condicionado das células leucêmicas, observouse um aumento na proliferação, formação capilar, migração e invasão das células RAEC. Além disso, o aumento nestes parâmetros foi maior em coculturas com a linhagem Lucena1. Em contrapartida, o prétratamento das células leucêmicas com violaceína reduziu significativamente estes efeitos, com inibição das vias VEGFR2/PI3K/AKT e VEGFR2/Src/MAPK nas linhagens estudadas (ECs e leucemias). Em conjunto, os resultados obtidos apontam a importância de fatores solúveis na modulação dos eventos associados ao processo angiogênico e demonstram o potencial antiangiogênico da violaceína com ação em vias importantes de regulação da angiogênese e proliferação celularDados abertos - Sucupira - Teses e dissertações (2018)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Universidade Federal de São Paulo (UNIFESP)Justo, Giselle Zenker [UNIFESP]Regatieri, Juliana Luporini Dreyfuss [UNIFESP]http://lattes.cnpq.br/2390066977030420http://lattes.cnpq.br/9147445236159161http://lattes.cnpq.br/0828096610832474Universidade Federal de São Paulo (UNIFESP)Palladino, Marcelly Valle [UNIFESP]2020-03-25T12:10:53Z2020-03-25T12:10:53Z2018-10-25info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion130 f.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=64331792018-0999.pdfhttps://repositorio.unifesp.br/handle/11600/53054porSão Pauloinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-10T16:55:05Zoai:repositorio.unifesp.br/:11600/53054Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-10T16:55:05Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais Investigation of antitumor and antiangiogênica activity of violacein in coculture of leucemic cells and endothelial cells |
title |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais |
spellingShingle |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais Palladino, Marcelly Valle [UNIFESP] L Leukemia Cancer LLeucemia Angiogenese Câncer Violaceína Violacein Angiogenesis |
title_short |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais |
title_full |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais |
title_fullStr |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais |
title_full_unstemmed |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais |
title_sort |
Investigação da atividade antitumoral e anti-angiogênica da violaceína em co-culturas de células leucêmicas e células endoteliais |
author |
Palladino, Marcelly Valle [UNIFESP] |
author_facet |
Palladino, Marcelly Valle [UNIFESP] |
author_role |
author |
dc.contributor.none.fl_str_mv |
Justo, Giselle Zenker [UNIFESP] Regatieri, Juliana Luporini Dreyfuss [UNIFESP] http://lattes.cnpq.br/2390066977030420 http://lattes.cnpq.br/9147445236159161 http://lattes.cnpq.br/0828096610832474 Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Palladino, Marcelly Valle [UNIFESP] |
dc.subject.por.fl_str_mv |
L Leukemia Cancer LLeucemia Angiogenese Câncer Violaceína Violacein Angiogenesis |
topic |
L Leukemia Cancer LLeucemia Angiogenese Câncer Violaceína Violacein Angiogenesis |
description |
Introduction: The bone marrow microenvironment is a milieu complex of various types of stromal and hematopoietic cells involved in the selfrenewal and differentiation of stem cells and hematopoietic progenitors (HSPC). Several soluble and membranebound factors produced by endothelial cells (EC) and perivascular stroma are crucial signals to maintain quiescence and facilitate the return to homeostasis after myeloablative chemotherapy. In addition, several studies have shown a relationship between HSPCs and ECs, pointing to hemangioblastic activity in HSPCs, both in the generation of cells and blood vessels. Considering the relationships between HSPCs and CSs in the bone marrow, it is possible to implicate CDEs in the establishment and progression of malignant HSPCs such as acute and chronic myeloid leukemias. In fact, in leukemias, studies have shown that angiogenesis also contributes to its pathogenesis, with an increase in bone marrow vascularization, associated with elevated levels of angiogenic factors. Thus, therapeutic strategies that aim to inhibit the angiogenic process may aid in the treatment of leukemia. OBJECTIVE: The objective of this study was to investigate the antiangiogenic effect of violacein on rabbit aortic endothelial cell (RAEC) and leukemic cells from the K562 and Lucena1 (K562 with MDR1 phenotype) lines. Results: It was observed that violacein, at concentrations lower than its IC 50, is able to inhibit capillary tube formation, proliferation, migration and invasion of ECs, with IC50 of RAEC cells (5.0 μM) higher than IC 50 Of the leukemic cells (3.5 μM). When RAEC cells were cocultured with leukemia cells in direct contact, in the presence of inserts or with the conditioned medium of the leukemic cells, an increase in proliferation, capillary formation, migration and invasion of RAEC cells was observed. In addition, the increase in these parameters was higher in cocultures with the Lucena1 lineage. In contrast, pretreatment of leukemic cells with violacein significantly reduced these effects, with inhibition of the VEGFR2 / PI3K / AKT and VEGFR2 / Src / MAPK pathways in the studied strains (ECs and leukemias). Taken together, the results show the importance of soluble factors in the modulation of the events associated with the angiogenic process and demonstrate the antiangiogenic potential of violacein with action in important ways of regulating angiogenesis and cell proliferation. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-10-25 2020-03-25T12:10:53Z 2020-03-25T12:10:53Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/doctoralThesis |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
doctoralThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6433179 2018-0999.pdf https://repositorio.unifesp.br/handle/11600/53054 |
url |
https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6433179 https://repositorio.unifesp.br/handle/11600/53054 |
identifier_str_mv |
2018-0999.pdf |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
130 f. application/pdf |
dc.coverage.none.fl_str_mv |
São Paulo |
dc.publisher.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
publisher.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268408932335616 |