Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell lines
Abstract Background: Mammary gland tumors are the most prevalent neoplasm in intact female dogs, and they are good natural models to study comparative oncology. Most canine mammary malignancies, as in women, are commonly refractory to conventional therapies and demand continuous new therapeutic ap...
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SciELO
2024-03-01
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Series: | Journal of Venomous Animals and Toxins including Tropical Diseases |
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author | Giovana Pedro Felipe César da Silva Brasileiro Jamile Mariano Macedo Andreimar Martins Soares Gabriel Caporale Mafra Carlos Eduardo Fonseca Alves Renée Laufer-Amorim |
author_facet | Giovana Pedro Felipe César da Silva Brasileiro Jamile Mariano Macedo Andreimar Martins Soares Gabriel Caporale Mafra Carlos Eduardo Fonseca Alves Renée Laufer-Amorim |
author_sort | Giovana Pedro |
collection | DOAJ |
description | Abstract Background: Mammary gland tumors are the most prevalent neoplasm in intact female dogs, and they are good natural models to study comparative oncology. Most canine mammary malignancies, as in women, are commonly refractory to conventional therapies and demand continuous new therapeutic approaches. Crotalus durissus terrificus, also called rattlesnake, has more than 60 different proteins in its venom with multiple pharmaceutical uses, such as antitumor, antiviral, and antimicrobial action. Crotoxin, a potent β-neurotoxin formed by the junction of two subunits, a basic subunit (CB-PLA2) and an acidic subunit (crotapotin), has already been reported to have anticancer properties in different types of cancers. Methods: In this work, we describe the cytotoxic potential of crotoxin and its subunits compared to doxorubicin (drug of choice) in two canine mammary carcinoma cell lines. Results: Crotoxin, CB-PLA2, crotalic venom, and doxorubicin decreased cell viability and the ability to migrate in a dose-dependent manner, and crotapotin did not present an antitumoral effect. For all compounds, the predominant cell death mechanism was apoptosis. In addition, crotoxin did not show toxicity in normal canine mammary gland cells. Conclusion: Therefore, this work showed that crotoxin and CB-PLA2 had cytotoxic activity, migration inhibition, and pro-apoptotic potential in canine mammary gland carcinoma cell lines, making their possible use in cancer research. |
first_indexed | 2024-04-24T22:38:09Z |
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id | doaj.art-9c01d4f906be44c99b73d0dd78cef056 |
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issn | 1678-9199 |
language | English |
last_indexed | 2024-04-24T22:38:09Z |
publishDate | 2024-03-01 |
publisher | SciELO |
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series | Journal of Venomous Animals and Toxins including Tropical Diseases |
spelling | doaj.art-9c01d4f906be44c99b73d0dd78cef0562024-03-19T07:39:21ZengSciELOJournal of Venomous Animals and Toxins including Tropical Diseases1678-91992024-03-013010.1590/1678-9199-jvatitd-2023-0062Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell linesGiovana Pedrohttps://orcid.org/0000-0001-8882-5223Felipe César da Silva BrasileiroJamile Mariano MacedoAndreimar Martins SoaresGabriel Caporale MafraCarlos Eduardo Fonseca Alveshttps://orcid.org/0000-0002-6702-6139Renée Laufer-AmorimAbstract Background: Mammary gland tumors are the most prevalent neoplasm in intact female dogs, and they are good natural models to study comparative oncology. Most canine mammary malignancies, as in women, are commonly refractory to conventional therapies and demand continuous new therapeutic approaches. Crotalus durissus terrificus, also called rattlesnake, has more than 60 different proteins in its venom with multiple pharmaceutical uses, such as antitumor, antiviral, and antimicrobial action. Crotoxin, a potent β-neurotoxin formed by the junction of two subunits, a basic subunit (CB-PLA2) and an acidic subunit (crotapotin), has already been reported to have anticancer properties in different types of cancers. Methods: In this work, we describe the cytotoxic potential of crotoxin and its subunits compared to doxorubicin (drug of choice) in two canine mammary carcinoma cell lines. Results: Crotoxin, CB-PLA2, crotalic venom, and doxorubicin decreased cell viability and the ability to migrate in a dose-dependent manner, and crotapotin did not present an antitumoral effect. For all compounds, the predominant cell death mechanism was apoptosis. In addition, crotoxin did not show toxicity in normal canine mammary gland cells. Conclusion: Therefore, this work showed that crotoxin and CB-PLA2 had cytotoxic activity, migration inhibition, and pro-apoptotic potential in canine mammary gland carcinoma cell lines, making their possible use in cancer research.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992024000100303&lng=en&tlng=enMammary tumorComparative oncologyCrotalus durissus terrificus venomBiological compounds |
spellingShingle | Giovana Pedro Felipe César da Silva Brasileiro Jamile Mariano Macedo Andreimar Martins Soares Gabriel Caporale Mafra Carlos Eduardo Fonseca Alves Renée Laufer-Amorim Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell lines Journal of Venomous Animals and Toxins including Tropical Diseases Mammary tumor Comparative oncology Crotalus durissus terrificus venom Biological compounds |
title | Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell lines |
title_full | Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell lines |
title_fullStr | Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell lines |
title_full_unstemmed | Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell lines |
title_short | Cytotoxic effects of crotoxin from Crotalus durissus terrificus snake in canine mammary tumor cell lines |
title_sort | cytotoxic effects of crotoxin from crotalus durissus terrificus snake in canine mammary tumor cell lines |
topic | Mammary tumor Comparative oncology Crotalus durissus terrificus venom Biological compounds |
url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992024000100303&lng=en&tlng=en |
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