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Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model
Various kinds of animal venoms and their components have been widely studied for potential therapeutic applications. This study evaluated whether Nemopilema nomurai jellyfish venom (NnV) has anticancer activity. NnV strongly induced cytotoxicity of HepG2 cells through apoptotic cell death, as demons...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530421/ https://www.ncbi.nlm.nih.gov/pubmed/28785288 http://dx.doi.org/10.1155/2017/2752716 |
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author | Lee, Hyunkyoung Bae, Seong Kyeong Kim, Munki Pyo, Min Jung Kim, Minkyung Yang, Sujeoung Won, Chung-kil Yoon, Won Duk Han, Chang Hoon Kang, Changkeun Kim, Euikyung |
author_facet | Lee, Hyunkyoung Bae, Seong Kyeong Kim, Munki Pyo, Min Jung Kim, Minkyung Yang, Sujeoung Won, Chung-kil Yoon, Won Duk Han, Chang Hoon Kang, Changkeun Kim, Euikyung |
author_sort | Lee, Hyunkyoung |
collection | PubMed |
description | Various kinds of animal venoms and their components have been widely studied for potential therapeutic applications. This study evaluated whether Nemopilema nomurai jellyfish venom (NnV) has anticancer activity. NnV strongly induced cytotoxicity of HepG2 cells through apoptotic cell death, as demonstrated by alterations of chromatic morphology, activation of procaspase-3, and an increase in the Bax/Bcl-2 ratio. Furthermore, NnV inhibited the phosphorylation of PI3K, PDK1, Akt, mTOR, p70S6K, and 4EBP1, whereas it enhanced the expression of p-PTEN. Interestingly, NnV also inactivated the negative feedback loops associated with Akt activation, as demonstrated by downregulation of Akt at Ser473 and mTOR at Ser2481. The anticancer effect of NnV was significant in a HepG2 xenograft mouse model, with no obvious toxicity. HepG2 cell death by NnV was inhibited by tetracycline, metalloprotease inhibitor, suggesting that metalloprotease component in NnV is closely related to the anticancer effects. This study demonstrates, for the first time, that NnV exerts highly selective cytotoxicity in HepG2 cells via dual inhibition of the Akt and mTOR signaling pathways, but not in normal cells. |
format | Online Article Text |
id | pubmed-5530421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-55304212017-08-07 Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model Lee, Hyunkyoung Bae, Seong Kyeong Kim, Munki Pyo, Min Jung Kim, Minkyung Yang, Sujeoung Won, Chung-kil Yoon, Won Duk Han, Chang Hoon Kang, Changkeun Kim, Euikyung Evid Based Complement Alternat Med Research Article Various kinds of animal venoms and their components have been widely studied for potential therapeutic applications. This study evaluated whether Nemopilema nomurai jellyfish venom (NnV) has anticancer activity. NnV strongly induced cytotoxicity of HepG2 cells through apoptotic cell death, as demonstrated by alterations of chromatic morphology, activation of procaspase-3, and an increase in the Bax/Bcl-2 ratio. Furthermore, NnV inhibited the phosphorylation of PI3K, PDK1, Akt, mTOR, p70S6K, and 4EBP1, whereas it enhanced the expression of p-PTEN. Interestingly, NnV also inactivated the negative feedback loops associated with Akt activation, as demonstrated by downregulation of Akt at Ser473 and mTOR at Ser2481. The anticancer effect of NnV was significant in a HepG2 xenograft mouse model, with no obvious toxicity. HepG2 cell death by NnV was inhibited by tetracycline, metalloprotease inhibitor, suggesting that metalloprotease component in NnV is closely related to the anticancer effects. This study demonstrates, for the first time, that NnV exerts highly selective cytotoxicity in HepG2 cells via dual inhibition of the Akt and mTOR signaling pathways, but not in normal cells. Hindawi 2017 2017-07-13 /pmc/articles/PMC5530421/ /pubmed/28785288 http://dx.doi.org/10.1155/2017/2752716 Text en Copyright © 2017 Hyunkyoung Lee et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lee, Hyunkyoung Bae, Seong Kyeong Kim, Munki Pyo, Min Jung Kim, Minkyung Yang, Sujeoung Won, Chung-kil Yoon, Won Duk Han, Chang Hoon Kang, Changkeun Kim, Euikyung Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model |
title | Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model |
title_full | Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model |
title_fullStr | Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model |
title_full_unstemmed | Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model |
title_short | Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model |
title_sort | anticancer effect of nemopilema nomurai jellyfish venom on hepg2 cells and a tumor xenograft animal model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530421/ https://www.ncbi.nlm.nih.gov/pubmed/28785288 http://dx.doi.org/10.1155/2017/2752716 |
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