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The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro

BACKGROUND: Breast cancer is a multifactorial disease that affects women worldwide. Its progression is likely to be executed by oxidative stress wherein elevated levels of reactive oxygen and nitrogen species drive several breast cancer pathologies. Spider venom contains various pharmacological pept...

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Autores principales: Lopez, Simon Miguel M, Aguilar, Jeremey S, Fernandez, Jerene Bashia B, Lao, Angelic Gayle J, Estrella, Mitzi Rain R, Devanadera, Mark Kevin P, Mayor, Anna Beatriz R, Jr, Leonardo A Guevarra, Santiago-Bautista, Myla R, Nuñeza, Olga M, Santiago, Librado A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771950/
https://www.ncbi.nlm.nih.gov/pubmed/32856874
http://dx.doi.org/10.31557/APJCP.2020.21.8.2423
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author Lopez, Simon Miguel M
Aguilar, Jeremey S
Fernandez, Jerene Bashia B
Lao, Angelic Gayle J
Estrella, Mitzi Rain R
Devanadera, Mark Kevin P
Mayor, Anna Beatriz R
Jr, Leonardo A Guevarra
Santiago-Bautista, Myla R
Nuñeza, Olga M
Santiago, Librado A
author_facet Lopez, Simon Miguel M
Aguilar, Jeremey S
Fernandez, Jerene Bashia B
Lao, Angelic Gayle J
Estrella, Mitzi Rain R
Devanadera, Mark Kevin P
Mayor, Anna Beatriz R
Jr, Leonardo A Guevarra
Santiago-Bautista, Myla R
Nuñeza, Olga M
Santiago, Librado A
author_sort Lopez, Simon Miguel M
collection PubMed
description BACKGROUND: Breast cancer is a multifactorial disease that affects women worldwide. Its progression is likely to be executed by oxidative stress wherein elevated levels of reactive oxygen and nitrogen species drive several breast cancer pathologies. Spider venom contains various pharmacological peptides which exhibit selective activity to abnormal expression of ion channels on cancer cell surface which can confer potent anti-cancer activities against this disease. METHODS: Venom was extracted from a Philippine tarantula by electrostimulation and fractionated by reverse phase-high performance liquid chromatography (RP-HPLC). Venom fractions were collected and used for in vitro analyses such as cellular toxicity, morphological assessment, and oxidative stress levels. RESULTS: The fractionation of crude spider venom generated several peaks which were predominantly detected spectrophotometrically and colorimetrically as peptides. Treatment of MCF-7 cell line of selected spider venom peptides induced production of several endogenous radicals such as hydroxyl radicals (•OH), nitric oxide radicals (•NO), superoxide anion radicals (•O(2−)) and lipid peroxides via malondialdehyde (MDA) reaction, which is comparable with the scavenging effects afforded by 400 µg/mL vitamin E and L-cysteine (p<0.05). Concomitantly, the free radicals produced decrease the mitochondrial membrane potential and metabolic activity as detected by rhodamine 123 and tetrazolium dye respectively (p>0.05). This is manifested by cytotoxicity in MCF-7 cells as seen by increase in membrane blebbing, cellular detachment, caspase activity and nuclear fragmentation. CONCLUSION: These data suggest that the Philippine tarantula venom contains peptide constituents exhibiting pro-oxidative and nitrosative-dependent cytotoxic activities against MCF-7 cells and can indicate mechanistic insights to further explore its potential application as prooxidants in cancer therapy.
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spelling pubmed-77719502021-02-06 The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro Lopez, Simon Miguel M Aguilar, Jeremey S Fernandez, Jerene Bashia B Lao, Angelic Gayle J Estrella, Mitzi Rain R Devanadera, Mark Kevin P Mayor, Anna Beatriz R Jr, Leonardo A Guevarra Santiago-Bautista, Myla R Nuñeza, Olga M Santiago, Librado A Asian Pac J Cancer Prev Research Article BACKGROUND: Breast cancer is a multifactorial disease that affects women worldwide. Its progression is likely to be executed by oxidative stress wherein elevated levels of reactive oxygen and nitrogen species drive several breast cancer pathologies. Spider venom contains various pharmacological peptides which exhibit selective activity to abnormal expression of ion channels on cancer cell surface which can confer potent anti-cancer activities against this disease. METHODS: Venom was extracted from a Philippine tarantula by electrostimulation and fractionated by reverse phase-high performance liquid chromatography (RP-HPLC). Venom fractions were collected and used for in vitro analyses such as cellular toxicity, morphological assessment, and oxidative stress levels. RESULTS: The fractionation of crude spider venom generated several peaks which were predominantly detected spectrophotometrically and colorimetrically as peptides. Treatment of MCF-7 cell line of selected spider venom peptides induced production of several endogenous radicals such as hydroxyl radicals (•OH), nitric oxide radicals (•NO), superoxide anion radicals (•O(2−)) and lipid peroxides via malondialdehyde (MDA) reaction, which is comparable with the scavenging effects afforded by 400 µg/mL vitamin E and L-cysteine (p<0.05). Concomitantly, the free radicals produced decrease the mitochondrial membrane potential and metabolic activity as detected by rhodamine 123 and tetrazolium dye respectively (p>0.05). This is manifested by cytotoxicity in MCF-7 cells as seen by increase in membrane blebbing, cellular detachment, caspase activity and nuclear fragmentation. CONCLUSION: These data suggest that the Philippine tarantula venom contains peptide constituents exhibiting pro-oxidative and nitrosative-dependent cytotoxic activities against MCF-7 cells and can indicate mechanistic insights to further explore its potential application as prooxidants in cancer therapy. West Asia Organization for Cancer Prevention 2020-08 /pmc/articles/PMC7771950/ /pubmed/32856874 http://dx.doi.org/10.31557/APJCP.2020.21.8.2423 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lopez, Simon Miguel M
Aguilar, Jeremey S
Fernandez, Jerene Bashia B
Lao, Angelic Gayle J
Estrella, Mitzi Rain R
Devanadera, Mark Kevin P
Mayor, Anna Beatriz R
Jr, Leonardo A Guevarra
Santiago-Bautista, Myla R
Nuñeza, Olga M
Santiago, Librado A
The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro
title The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro
title_full The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro
title_fullStr The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro
title_full_unstemmed The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro
title_short The Venom of Philippine Tarantula (Theraphosidae) Contains Peptides with Pro-Oxidative and Nitrosative-Dependent Cytotoxic Activities against Breast Cancer Cells (MCF-7) In Vitro
title_sort venom of philippine tarantula (theraphosidae) contains peptides with pro-oxidative and nitrosative-dependent cytotoxic activities against breast cancer cells (mcf-7) in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771950/
https://www.ncbi.nlm.nih.gov/pubmed/32856874
http://dx.doi.org/10.31557/APJCP.2020.21.8.2423
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