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Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells
Açai fruit has been studied for its antioxidant properties, with positive feedback against many diseases, including cancer. Although açai seeds are not edible, their composition has been studied in order to find new applications and reduce garbage generation. This study aimed to evaluate the cytotox...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262440/ https://www.ncbi.nlm.nih.gov/pubmed/30373103 http://dx.doi.org/10.3390/foods7110178 |
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author | Martinez, Raquel Martins Guimarães, Deborah de Almeida Bauer Berniz, Camila Ramos de Abreu, Joel Pimentel da Rocha, Ana Paula Machado de Moura, Roberto Soares Resende, Angela Castro Teodoro, Anderson Junger |
author_facet | Martinez, Raquel Martins Guimarães, Deborah de Almeida Bauer Berniz, Camila Ramos de Abreu, Joel Pimentel da Rocha, Ana Paula Machado de Moura, Roberto Soares Resende, Angela Castro Teodoro, Anderson Junger |
author_sort | Martinez, Raquel Martins |
collection | PubMed |
description | Açai fruit has been studied for its antioxidant properties, with positive feedback against many diseases, including cancer. Although açai seeds are not edible, their composition has been studied in order to find new applications and reduce garbage generation. This study aimed to evaluate the cytotoxic effects and impacts on the cell cycle and apoptosis of açai seed extract (ASE) on human lung carcinoma cell line (A549). Antioxidant activity of açai seed extract (ASE) was measured by DPPH assay, Trolox Equivalent Antioxidant Capacity (ABTS/TEAC), Ferric Reducing Ability (FRAP) and Oxygen radical absorbance capacity (ORAC) assays. Human lung carcinoma cell viability (A549) was monitored by MTT assay method and the effects on cell cycle and apoptosis were measured by flow cytometry. The results indicate high antioxidant activity in ASE and high values of total phenolic compounds (37.08 ± 8.56 g gallic acid/100 g). The MTT assay showed a maximum decrease (72.07%) in the viability of A549 cells after 48 h treatment with ASE (200 µg/mL). Flow cytometer analysis revealed that ASE increased the percentage of cells in G0/G1 phase and promoted a high increase of apoptotic cells when compared to the untreated cells. The present study suggests that ASE has a high antioxidant capacity and may have a protective effect against lung cancer. |
format | Online Article Text |
id | pubmed-6262440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62624402018-12-05 Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells Martinez, Raquel Martins Guimarães, Deborah de Almeida Bauer Berniz, Camila Ramos de Abreu, Joel Pimentel da Rocha, Ana Paula Machado de Moura, Roberto Soares Resende, Angela Castro Teodoro, Anderson Junger Foods Communication Açai fruit has been studied for its antioxidant properties, with positive feedback against many diseases, including cancer. Although açai seeds are not edible, their composition has been studied in order to find new applications and reduce garbage generation. This study aimed to evaluate the cytotoxic effects and impacts on the cell cycle and apoptosis of açai seed extract (ASE) on human lung carcinoma cell line (A549). Antioxidant activity of açai seed extract (ASE) was measured by DPPH assay, Trolox Equivalent Antioxidant Capacity (ABTS/TEAC), Ferric Reducing Ability (FRAP) and Oxygen radical absorbance capacity (ORAC) assays. Human lung carcinoma cell viability (A549) was monitored by MTT assay method and the effects on cell cycle and apoptosis were measured by flow cytometry. The results indicate high antioxidant activity in ASE and high values of total phenolic compounds (37.08 ± 8.56 g gallic acid/100 g). The MTT assay showed a maximum decrease (72.07%) in the viability of A549 cells after 48 h treatment with ASE (200 µg/mL). Flow cytometer analysis revealed that ASE increased the percentage of cells in G0/G1 phase and promoted a high increase of apoptotic cells when compared to the untreated cells. The present study suggests that ASE has a high antioxidant capacity and may have a protective effect against lung cancer. MDPI 2018-10-26 /pmc/articles/PMC6262440/ /pubmed/30373103 http://dx.doi.org/10.3390/foods7110178 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Martinez, Raquel Martins Guimarães, Deborah de Almeida Bauer Berniz, Camila Ramos de Abreu, Joel Pimentel da Rocha, Ana Paula Machado de Moura, Roberto Soares Resende, Angela Castro Teodoro, Anderson Junger Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells |
title | Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells |
title_full | Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells |
title_fullStr | Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells |
title_full_unstemmed | Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells |
title_short | Açai (Euterpe oleracea Mart.) Seed Extract Induces Cell Cycle Arrest and Apoptosis in Human Lung Carcinoma Cells |
title_sort | açai (euterpe oleracea mart.) seed extract induces cell cycle arrest and apoptosis in human lung carcinoma cells |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262440/ https://www.ncbi.nlm.nih.gov/pubmed/30373103 http://dx.doi.org/10.3390/foods7110178 |
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