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Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines

Snake venom possesses various kinds of proteins and neurotoxic polypeptides, which can negatively interfere with the neurotransmitter signaling cascade. This phenomenon occurs mainly due to the blocking of ion channels in the body system. Envenomation prevents or severely interrupts nerve impulses f...

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Autores principales: Al-Asmari, Abdulrahman Khazim, Riyasdeen, Anvarbatcha, Al-Shahrani, Mohammad Hamed, Islam, Mozaffarul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079696/
https://www.ncbi.nlm.nih.gov/pubmed/27799796
http://dx.doi.org/10.2147/OTT.S115055
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author Al-Asmari, Abdulrahman Khazim
Riyasdeen, Anvarbatcha
Al-Shahrani, Mohammad Hamed
Islam, Mozaffarul
author_facet Al-Asmari, Abdulrahman Khazim
Riyasdeen, Anvarbatcha
Al-Shahrani, Mohammad Hamed
Islam, Mozaffarul
author_sort Al-Asmari, Abdulrahman Khazim
collection PubMed
description Snake venom possesses various kinds of proteins and neurotoxic polypeptides, which can negatively interfere with the neurotransmitter signaling cascade. This phenomenon occurs mainly due to the blocking of ion channels in the body system. Envenomation prevents or severely interrupts nerve impulses from being transmitted, inhibition of adenosine triphosphate synthesis, and proper functioning of the cardiac muscles. However, some beneficial properties of venoms have also been reported. The aim of this study was to examine the snake venom as an anticancer agent due to its inhibitory effects on cancer progression such as cell motility, cell invasion, and colony formation. In this study, the effect of venoms on phenotypic changes and the change on molecular level in colorectal and breast cancer cell lines were examined. A reduction of 60%–90% in cell motility, colony formation, and cell invasion was observed when these cell lines were treated with different concentrations of snake venom. In addition, the increase in oxidative stress that results in an increase in the number of apoptotic cancer cells was significantly higher in the venom-treated cell lines. Further analysis showed that there was a decrease in the expression of pro-inflammatory cytokines and signaling proteins, strongly suggesting a promising role for snake venom against breast and colorectal cancer cell progression. In conclusion, the snake venoms used in this study showed significant anticancer properties against colorectal and breast cancer cell lines.
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spelling pubmed-50796962016-10-31 Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines Al-Asmari, Abdulrahman Khazim Riyasdeen, Anvarbatcha Al-Shahrani, Mohammad Hamed Islam, Mozaffarul Onco Targets Ther Original Research Snake venom possesses various kinds of proteins and neurotoxic polypeptides, which can negatively interfere with the neurotransmitter signaling cascade. This phenomenon occurs mainly due to the blocking of ion channels in the body system. Envenomation prevents or severely interrupts nerve impulses from being transmitted, inhibition of adenosine triphosphate synthesis, and proper functioning of the cardiac muscles. However, some beneficial properties of venoms have also been reported. The aim of this study was to examine the snake venom as an anticancer agent due to its inhibitory effects on cancer progression such as cell motility, cell invasion, and colony formation. In this study, the effect of venoms on phenotypic changes and the change on molecular level in colorectal and breast cancer cell lines were examined. A reduction of 60%–90% in cell motility, colony formation, and cell invasion was observed when these cell lines were treated with different concentrations of snake venom. In addition, the increase in oxidative stress that results in an increase in the number of apoptotic cancer cells was significantly higher in the venom-treated cell lines. Further analysis showed that there was a decrease in the expression of pro-inflammatory cytokines and signaling proteins, strongly suggesting a promising role for snake venom against breast and colorectal cancer cell progression. In conclusion, the snake venoms used in this study showed significant anticancer properties against colorectal and breast cancer cell lines. Dove Medical Press 2016-10-20 /pmc/articles/PMC5079696/ /pubmed/27799796 http://dx.doi.org/10.2147/OTT.S115055 Text en © 2016 Al-Asmari et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Al-Asmari, Abdulrahman Khazim
Riyasdeen, Anvarbatcha
Al-Shahrani, Mohammad Hamed
Islam, Mozaffarul
Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines
title Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines
title_full Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines
title_fullStr Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines
title_full_unstemmed Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines
title_short Snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines
title_sort snake venom causes apoptosis by increasing the reactive oxygen species in colorectal and breast cancer cell lines
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079696/
https://www.ncbi.nlm.nih.gov/pubmed/27799796
http://dx.doi.org/10.2147/OTT.S115055
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