Avaliação in vitro da atividade anticancerígena de compostos naturais e semissintéticos contra neoplasias hematológicas

• Ano de defesa: 2020
• Autor(a) principal: Oliveira, Regiane Costa de
• Tipo de documento: Dissertação
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade do Estado do Amazonas; Brasil; UEA; PPGH -PROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS APLICADAS À HEMATOLOGIA
• Palavras-chave em Português: Fitoterápicos; Leucemias; Neoplasias; Bioprospecção
• Link de acesso: https://ri.uea.edu.br/handle/riuea/2250

Hematological neoplasms are a heterogeneous group of diseases originating in the bone marrow that present as main tumors of lymphoid and hematopoietic tissues leukemias, lymphomas and myelomas. The main current treatments include chemotherapy and radiation therapy. However, most of these treatments are expensive and result in intense side effects for patients, which demands new safer and more cost-effective therapeutic alternatives. The purpose of this study was to investigate the in vitro anticancer and imunomodulatory activities of natural and semi-synthetic compounds against hematological neoplasms. As human normal peripheral blood mononucleated cells (PBMC) was used in the assays, this project was duly approved by the Research Ethics Committee (CEP) of the HEMOAM Foundation, according to the guidelines recommended by the resolution 466/2012 of the Ministry of Health. First, PBMC and Vero cells were treated with different concentrations of the following compounds: Br- Ell-S03Na, pyrazoloisoquinoline, Z1 and Z2. The cytotoxicity was assessed using the K562, HL-60 and U937 cell lines. All substances tested showed anticancer activity, without significant cytotoxic effect against non-cancerous cells. The substance that showed the best anticancer activity was a derivative of zerumbone (Z1) that had an IC50 value of 5.20μM in HL-60 cells. Regarding the cell cycle, it was observed that the substances Z1 and pyrazoloisoquinoline induced greater capture of cells in the G1 phase of the cell cycle, while in relation to the substance Br-Ell-S03Na and Z2, a higher proportion of capture was observed in the S and G2 phases, respectively. The substances Br-Ell-S03Na and pyrazoloisoquinoline induced the expression of IL-6, but inhibited the expression of IL-8. The Z2 substance also inhibited the expression of IL-8. The results presented by this study demonstrate that the analyzed substances have an important anticancer and immunomodulatory potential, which make them possible candidates to be explored in prospective in vivo studies