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Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation

Piperine (1-piperoylpeperdine), a nitrogenous pungent substance, is present in the fruits of black pepper (Piper nigrum Linn.) and long pepper (Piper longum Linn.). It possesses several pharmacological properties and has been extensively explored for its anti-cancerous activities. The mechanism unde...

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Autores principales: Jafri, Asif, Siddiqui, Sahabjada, Rais, Juhi, Ahmad, Md Sultan, Kumar, Sudhir, Jafar, Tabrez, Afzal, Mohammad, Arshad, Md
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558508/
https://www.ncbi.nlm.nih.gov/pubmed/31217779
http://dx.doi.org/10.17179/excli2018-1928
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author Jafri, Asif
Siddiqui, Sahabjada
Rais, Juhi
Ahmad, Md Sultan
Kumar, Sudhir
Jafar, Tabrez
Afzal, Mohammad
Arshad, Md
author_facet Jafri, Asif
Siddiqui, Sahabjada
Rais, Juhi
Ahmad, Md Sultan
Kumar, Sudhir
Jafar, Tabrez
Afzal, Mohammad
Arshad, Md
author_sort Jafri, Asif
collection PubMed
description Piperine (1-piperoylpeperdine), a nitrogenous pungent substance, is present in the fruits of black pepper (Piper nigrum Linn.) and long pepper (Piper longum Linn.). It possesses several pharmacological properties and has been extensively explored for its anti-cancerous activities. The mechanism underlying its anti-cancer potential in human cervical adenocarcinoma (HeLa) cells is not well interpreted. The anti-proliferative effect and the mode of action of piperine were investigated through some potent markers of apoptosis viz.reactive oxygen species (ROS) generation, cellular apoptosis and loss of mitochondrial membrane potential (MMP). DNA fragmentation, cell cycle kinetics, caspase-3 activity and cell migration assays were also conducted to observe the efficacy of piperine against HeLa cells. The results showed that piperine exposure induces apoptosis significantly in a dose-dependent manner and inhibits the growth of HeLa cells with an increase in ROS generation, nuclear condensation and delayed wound healing. In addition, piperine also encourages cell death by the loss of MMP, DNA fragmentation and the activation of caspase-3. Growth inhibition of HeLa cells was found to be associated with G2/M phase arrest and sub-G1 accumulation. The present study provides useful insight into the apoptotic potential of piperine and further in vivo and clinical studies will be needed for its validation and in the finding of more effective and least toxic regimens against cervical cancer.
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spelling pubmed-65585082019-06-19 Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation Jafri, Asif Siddiqui, Sahabjada Rais, Juhi Ahmad, Md Sultan Kumar, Sudhir Jafar, Tabrez Afzal, Mohammad Arshad, Md EXCLI J Original Article Piperine (1-piperoylpeperdine), a nitrogenous pungent substance, is present in the fruits of black pepper (Piper nigrum Linn.) and long pepper (Piper longum Linn.). It possesses several pharmacological properties and has been extensively explored for its anti-cancerous activities. The mechanism underlying its anti-cancer potential in human cervical adenocarcinoma (HeLa) cells is not well interpreted. The anti-proliferative effect and the mode of action of piperine were investigated through some potent markers of apoptosis viz.reactive oxygen species (ROS) generation, cellular apoptosis and loss of mitochondrial membrane potential (MMP). DNA fragmentation, cell cycle kinetics, caspase-3 activity and cell migration assays were also conducted to observe the efficacy of piperine against HeLa cells. The results showed that piperine exposure induces apoptosis significantly in a dose-dependent manner and inhibits the growth of HeLa cells with an increase in ROS generation, nuclear condensation and delayed wound healing. In addition, piperine also encourages cell death by the loss of MMP, DNA fragmentation and the activation of caspase-3. Growth inhibition of HeLa cells was found to be associated with G2/M phase arrest and sub-G1 accumulation. The present study provides useful insight into the apoptotic potential of piperine and further in vivo and clinical studies will be needed for its validation and in the finding of more effective and least toxic regimens against cervical cancer. Leibniz Research Centre for Working Environment and Human Factors 2019-03-13 /pmc/articles/PMC6558508/ /pubmed/31217779 http://dx.doi.org/10.17179/excli2018-1928 Text en Copyright © 2019 Jafri et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Jafri, Asif
Siddiqui, Sahabjada
Rais, Juhi
Ahmad, Md Sultan
Kumar, Sudhir
Jafar, Tabrez
Afzal, Mohammad
Arshad, Md
Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation
title Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation
title_full Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation
title_fullStr Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation
title_full_unstemmed Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation
title_short Induction of apoptosis by piperine in human cervical adenocarcinoma via ROS mediated mitochondrial pathway and caspase-3 activation
title_sort induction of apoptosis by piperine in human cervical adenocarcinoma via ros mediated mitochondrial pathway and caspase-3 activation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558508/
https://www.ncbi.nlm.nih.gov/pubmed/31217779
http://dx.doi.org/10.17179/excli2018-1928
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