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Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells

BACKGROUND: Pomegranate (Punica granatum) is currently a member of Lythraceae family which has potentially cytotoxic activities. Numerous studies have been done on cytotoxic components of pomegranate's juices, barks and leaves. The peels, which considered as a waste, contain higher antioxidant...

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Autores principales: Asmaa, Mat Jusoh Siti, Ali, Al-Jamal Hamid, Farid, Johan Muhammad, Azman, Seeni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456882/
https://www.ncbi.nlm.nih.gov/pubmed/26097816
http://dx.doi.org/10.4103/2229-516X.157154
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author Asmaa, Mat Jusoh Siti
Ali, Al-Jamal Hamid
Farid, Johan Muhammad
Azman, Seeni
author_facet Asmaa, Mat Jusoh Siti
Ali, Al-Jamal Hamid
Farid, Johan Muhammad
Azman, Seeni
author_sort Asmaa, Mat Jusoh Siti
collection PubMed
description BACKGROUND: Pomegranate (Punica granatum) is currently a member of Lythraceae family which has potentially cytotoxic activities. Numerous studies have been done on cytotoxic components of pomegranate's juices, barks and leaves. The peels, which considered as a waste, contain higher antioxidant components compared with other parts of the plant. AIM: To investigate the potential anti-cancer activity of pomegranate peel on growth and cell death mechanisms of chronic myeloid leukemic (CML) cells, K562. MATERIALS AND METHODS: Punica granatum peels extract (PGPE) was extracted by successive ethanol extraction, 80% (v/v), freeze dried, diluted to 20 mg/mL working concentration and was subjected to phytochemical screening. K562 cell was treated with crude PGPE for 72 h. Following IC(50) concentration, the apoptosis, cell cycle and protein analysis were evaluated. Cell growth inhibition assay was performed by conventional trypan blue exclusion assay. Apoptosis and cell cycle were analyzed by flow-cytometry using BD apoptosis and cell cycle kits and protein analysis by western blotting. All the results are expressed as mean ± standard error of mean of three independent experiments. Statistical analysis was performed by nonparametric Mann-Whitney U-test. RESULTS: Results demonstrated that PGPE promotes growth inhibition of K562 cells mainly via G2/M phase arrest while still conserving apoptosis induction, but at a lower rate. Apoptosis activities were proposed by the up-regulation of caspases and cytochrome c with an elevated level of p21 and p53. CONCLUSION: PGPE caused an inhibition in cell proliferation of CML cell mainly by cell cycle arrest.
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spelling pubmed-44568822015-06-19 Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells Asmaa, Mat Jusoh Siti Ali, Al-Jamal Hamid Farid, Johan Muhammad Azman, Seeni Int J Appl Basic Med Res Original Article BACKGROUND: Pomegranate (Punica granatum) is currently a member of Lythraceae family which has potentially cytotoxic activities. Numerous studies have been done on cytotoxic components of pomegranate's juices, barks and leaves. The peels, which considered as a waste, contain higher antioxidant components compared with other parts of the plant. AIM: To investigate the potential anti-cancer activity of pomegranate peel on growth and cell death mechanisms of chronic myeloid leukemic (CML) cells, K562. MATERIALS AND METHODS: Punica granatum peels extract (PGPE) was extracted by successive ethanol extraction, 80% (v/v), freeze dried, diluted to 20 mg/mL working concentration and was subjected to phytochemical screening. K562 cell was treated with crude PGPE for 72 h. Following IC(50) concentration, the apoptosis, cell cycle and protein analysis were evaluated. Cell growth inhibition assay was performed by conventional trypan blue exclusion assay. Apoptosis and cell cycle were analyzed by flow-cytometry using BD apoptosis and cell cycle kits and protein analysis by western blotting. All the results are expressed as mean ± standard error of mean of three independent experiments. Statistical analysis was performed by nonparametric Mann-Whitney U-test. RESULTS: Results demonstrated that PGPE promotes growth inhibition of K562 cells mainly via G2/M phase arrest while still conserving apoptosis induction, but at a lower rate. Apoptosis activities were proposed by the up-regulation of caspases and cytochrome c with an elevated level of p21 and p53. CONCLUSION: PGPE caused an inhibition in cell proliferation of CML cell mainly by cell cycle arrest. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4456882/ /pubmed/26097816 http://dx.doi.org/10.4103/2229-516X.157154 Text en Copyright: © International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Asmaa, Mat Jusoh Siti
Ali, Al-Jamal Hamid
Farid, Johan Muhammad
Azman, Seeni
Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells
title Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells
title_full Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells
title_fullStr Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells
title_full_unstemmed Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells
title_short Growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, K562 cells
title_sort growth inhibitory effects of crude pomegranate peel extract on chronic myeloid leukemia, k562 cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456882/
https://www.ncbi.nlm.nih.gov/pubmed/26097816
http://dx.doi.org/10.4103/2229-516X.157154
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