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Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway

Cancer has been recognized as one of the life-threating diseases. Breast cancer is a leading cause of mortality among women. In spite of current developments in the therapy and diagnosis of cancer, the survival rate is still less. Recently, plant-derived natural products gain attention as anticancer...

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Autores principales: Al-Oqail, Mai M., Al-Sheddi, Ebtesam S., Farshori, Nida N., Al-Massarani, Shaza M., Al-Turki, Eman A., Ahmad, Javed, Al-Khedhairy, Abdulaziz A., Siddiqui, Maqsood A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855084/
https://www.ncbi.nlm.nih.gov/pubmed/31781357
http://dx.doi.org/10.1155/2019/9789241
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author Al-Oqail, Mai M.
Al-Sheddi, Ebtesam S.
Farshori, Nida N.
Al-Massarani, Shaza M.
Al-Turki, Eman A.
Ahmad, Javed
Al-Khedhairy, Abdulaziz A.
Siddiqui, Maqsood A.
author_facet Al-Oqail, Mai M.
Al-Sheddi, Ebtesam S.
Farshori, Nida N.
Al-Massarani, Shaza M.
Al-Turki, Eman A.
Ahmad, Javed
Al-Khedhairy, Abdulaziz A.
Siddiqui, Maqsood A.
author_sort Al-Oqail, Mai M.
collection PubMed
description Cancer has been recognized as one of the life-threating diseases. Breast cancer is a leading cause of mortality among women. In spite of current developments in the therapy and diagnosis of cancer, the survival rate is still less. Recently, plant-derived natural products gain attention as anticancer agents due to the nontoxic nature. Therefore, the aim of present study was to investigate the anticancer capacity of corn silk extract (CSE) on human breast cancer (MCF-7) and normal human mesenchymal (hMSC-TERT4) cells. Following 24 h treatment to corn silk extract, the cytotoxicity was assessed by MTT, NRU, and morphological assays. The oxidative stress markers (GSH and LPO), ROS production, MMP change, and expression of apoptotic marker genes (p53, Bax, Bcl-2, caspase-3, and caspase-9) were also studied in MCF-7 cells treated at 250 to 1000 μg/ml of CSE for 24 h. Our results showed that CSE decreased the cell viability and increased the apoptosis in a dose-dependent manner. The level of LPO and ROS production was found significantly higher; however, GSH and MMP level was observed lower in CSE-treated MCF-7 cells. The real-time PCR data showed a significant upregulation in p53, Bax, caspase-3, and caspase-9 and downregulation in the mRNA expression of Bcl-2 genes in MCF-7 cells exposed to CSE. Collectively, the data from this study stated that corn silk extract induced apoptosis via the ROS-mediated mitochondrial pathway in MCF-7 cells.
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spelling pubmed-68550842019-11-28 Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway Al-Oqail, Mai M. Al-Sheddi, Ebtesam S. Farshori, Nida N. Al-Massarani, Shaza M. Al-Turki, Eman A. Ahmad, Javed Al-Khedhairy, Abdulaziz A. Siddiqui, Maqsood A. Oxid Med Cell Longev Research Article Cancer has been recognized as one of the life-threating diseases. Breast cancer is a leading cause of mortality among women. In spite of current developments in the therapy and diagnosis of cancer, the survival rate is still less. Recently, plant-derived natural products gain attention as anticancer agents due to the nontoxic nature. Therefore, the aim of present study was to investigate the anticancer capacity of corn silk extract (CSE) on human breast cancer (MCF-7) and normal human mesenchymal (hMSC-TERT4) cells. Following 24 h treatment to corn silk extract, the cytotoxicity was assessed by MTT, NRU, and morphological assays. The oxidative stress markers (GSH and LPO), ROS production, MMP change, and expression of apoptotic marker genes (p53, Bax, Bcl-2, caspase-3, and caspase-9) were also studied in MCF-7 cells treated at 250 to 1000 μg/ml of CSE for 24 h. Our results showed that CSE decreased the cell viability and increased the apoptosis in a dose-dependent manner. The level of LPO and ROS production was found significantly higher; however, GSH and MMP level was observed lower in CSE-treated MCF-7 cells. The real-time PCR data showed a significant upregulation in p53, Bax, caspase-3, and caspase-9 and downregulation in the mRNA expression of Bcl-2 genes in MCF-7 cells exposed to CSE. Collectively, the data from this study stated that corn silk extract induced apoptosis via the ROS-mediated mitochondrial pathway in MCF-7 cells. Hindawi 2019-10-20 /pmc/articles/PMC6855084/ /pubmed/31781357 http://dx.doi.org/10.1155/2019/9789241 Text en Copyright © 2019 Mai M. Al-Oqail et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Al-Oqail, Mai M.
Al-Sheddi, Ebtesam S.
Farshori, Nida N.
Al-Massarani, Shaza M.
Al-Turki, Eman A.
Ahmad, Javed
Al-Khedhairy, Abdulaziz A.
Siddiqui, Maqsood A.
Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway
title Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway
title_full Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway
title_fullStr Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway
title_full_unstemmed Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway
title_short Corn Silk (Zea mays L.) Induced Apoptosis in Human Breast Cancer (MCF-7) Cells via the ROS-Mediated Mitochondrial Pathway
title_sort corn silk (zea mays l.) induced apoptosis in human breast cancer (mcf-7) cells via the ros-mediated mitochondrial pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855084/
https://www.ncbi.nlm.nih.gov/pubmed/31781357
http://dx.doi.org/10.1155/2019/9789241
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