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Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress

Due to the lack of chemotherapeutic drugs that selectively affect cervical cancer cells, natural sources such as snake venom are currently being investigated for molecules with antitumor potential. Pllans–II, a phospholipase A(2) type–Asp49 from Porthidium lansbergii lansbergii snake venom, induced...

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Autores principales: Montoya-Gómez, Alejandro, Rivera Franco, Nelson, Montealegre-Sanchez, Leonel Ives, Solano-Redondo, Luis Manuel, Castillo, Andrés, Mosquera-Escudero, Mildrey, Jiménez-Charris, Eliécer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573087/
https://www.ncbi.nlm.nih.gov/pubmed/36235027
http://dx.doi.org/10.3390/molecules27196491
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author Montoya-Gómez, Alejandro
Rivera Franco, Nelson
Montealegre-Sanchez, Leonel Ives
Solano-Redondo, Luis Manuel
Castillo, Andrés
Mosquera-Escudero, Mildrey
Jiménez-Charris, Eliécer
author_facet Montoya-Gómez, Alejandro
Rivera Franco, Nelson
Montealegre-Sanchez, Leonel Ives
Solano-Redondo, Luis Manuel
Castillo, Andrés
Mosquera-Escudero, Mildrey
Jiménez-Charris, Eliécer
author_sort Montoya-Gómez, Alejandro
collection PubMed
description Due to the lack of chemotherapeutic drugs that selectively affect cervical cancer cells, natural sources such as snake venom are currently being investigated for molecules with antitumor potential. Pllans–II, a phospholipase A(2) type–Asp49 from Porthidium lansbergii lansbergii snake venom, induced cell death in a cervical cancer cell line—Ca Ski—related to dysfunction in the ability to resolve endoplasmic reticulum stress, evidenced by sub–expression of genes such as PERK, ERO1 PDIs, HSP70, and CHOP. Western blot analysis validated the last two genes′ sub–expression at the protein level. In addition, Pllans–II presented a dose–dependent cytotoxic effect on cancer cells and an insignificant effect on healthy endothelial cells (HUVEC). Additionally, Pllans–II inhibited cancer cells′ adhesion and migration capacity, induced cell cycle arrest in the G2/M phase, and induced apoptosis stimulated possibly by the extrinsic route. These results demonstrate for the first time that Pllans–II has an antitumor effect on a squamous epithelial cervical cancer cell line and represents a possible biotechnological tool for designing a prominent antitumor agent.
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spelling pubmed-95730872022-10-17 Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress Montoya-Gómez, Alejandro Rivera Franco, Nelson Montealegre-Sanchez, Leonel Ives Solano-Redondo, Luis Manuel Castillo, Andrés Mosquera-Escudero, Mildrey Jiménez-Charris, Eliécer Molecules Article Due to the lack of chemotherapeutic drugs that selectively affect cervical cancer cells, natural sources such as snake venom are currently being investigated for molecules with antitumor potential. Pllans–II, a phospholipase A(2) type–Asp49 from Porthidium lansbergii lansbergii snake venom, induced cell death in a cervical cancer cell line—Ca Ski—related to dysfunction in the ability to resolve endoplasmic reticulum stress, evidenced by sub–expression of genes such as PERK, ERO1 PDIs, HSP70, and CHOP. Western blot analysis validated the last two genes′ sub–expression at the protein level. In addition, Pllans–II presented a dose–dependent cytotoxic effect on cancer cells and an insignificant effect on healthy endothelial cells (HUVEC). Additionally, Pllans–II inhibited cancer cells′ adhesion and migration capacity, induced cell cycle arrest in the G2/M phase, and induced apoptosis stimulated possibly by the extrinsic route. These results demonstrate for the first time that Pllans–II has an antitumor effect on a squamous epithelial cervical cancer cell line and represents a possible biotechnological tool for designing a prominent antitumor agent. MDPI 2022-10-01 /pmc/articles/PMC9573087/ /pubmed/36235027 http://dx.doi.org/10.3390/molecules27196491 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Montoya-Gómez, Alejandro
Rivera Franco, Nelson
Montealegre-Sanchez, Leonel Ives
Solano-Redondo, Luis Manuel
Castillo, Andrés
Mosquera-Escudero, Mildrey
Jiménez-Charris, Eliécer
Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress
title Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress
title_full Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress
title_fullStr Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress
title_full_unstemmed Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress
title_short Pllans–II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress
title_sort pllans–ii induces cell death in cervical cancer squamous epithelial cells via unfolded protein accumulation and endoplasmic reticulum stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573087/
https://www.ncbi.nlm.nih.gov/pubmed/36235027
http://dx.doi.org/10.3390/molecules27196491
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