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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9573087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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