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Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos

In this study, we showed that crude extract of Anisomeles indica (AI-EtE) expressed its toxicity to HeLa cells with an IC50 dose of 38.8 µg/mL and to zebrafish embryos with malformations, lethality and hatching inhibition at 72-hpf at doses higher than 75 µg/mL. More interestingly, flow cytometry re...

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Autores principales: Bich-Loan, Nguyen T., Kien, Kieu Trung, Thanh, Nguyen Lai, Kim-Thanh, Nguyen T., Huy, Nguyen Quang, The-Hai, Pham, Muller, Marc, Nachtergael, Amandine, Duez, Pierre, Thang, Nguyen Dinh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8003830/
https://www.ncbi.nlm.nih.gov/pubmed/33804714
http://dx.doi.org/10.3390/life11030257
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author Bich-Loan, Nguyen T.
Kien, Kieu Trung
Thanh, Nguyen Lai
Kim-Thanh, Nguyen T.
Huy, Nguyen Quang
The-Hai, Pham
Muller, Marc
Nachtergael, Amandine
Duez, Pierre
Thang, Nguyen Dinh
author_facet Bich-Loan, Nguyen T.
Kien, Kieu Trung
Thanh, Nguyen Lai
Kim-Thanh, Nguyen T.
Huy, Nguyen Quang
The-Hai, Pham
Muller, Marc
Nachtergael, Amandine
Duez, Pierre
Thang, Nguyen Dinh
author_sort Bich-Loan, Nguyen T.
collection PubMed
description In this study, we showed that crude extract of Anisomeles indica (AI-EtE) expressed its toxicity to HeLa cells with an IC50 dose of 38.8 µg/mL and to zebrafish embryos with malformations, lethality and hatching inhibition at 72-hpf at doses higher than 75 µg/mL. More interestingly, flow cytometry revealed that AI-EtE significantly promoted the number of cells entering apoptotic. Accordingly, the transcript levels of BAX, CASPASE-8, and CASPASE-3 in the cells treated with AI-EtE at IC50 dose were 1.55-, 1.62-, and 2.45-fold higher than those in the control cells, respectively. Moreover, treatment with AI-EtE caused cell cycle arrest at the G1 phase in a p53-independent manner. Particularly, percentages of AI-EtE-treated cells in G1, S, G2/M were, respectively 85%, 6.7% and 6.4%; while percentages of control cells in G1, S, G2/M were 64%, 15% and 19%, respectively. Consistent with cell cycle arrest, the expressions of CDKN1A and CDNK2A in AI-EtE-treated cells were up-regulated 1.9- and 1.64-fold, respectively. Significantly, treatment with AI-EtE also decreased anchorage-independent growth of HeLa cells. In conclusion, we suggest that Anisomeles indica can be considered as a medicinal plant with a possible use against cervical cancer cells; however, the used dose should be carefully monitored, especially when applying to pregnant women.
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spelling pubmed-80038302021-03-28 Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos Bich-Loan, Nguyen T. Kien, Kieu Trung Thanh, Nguyen Lai Kim-Thanh, Nguyen T. Huy, Nguyen Quang The-Hai, Pham Muller, Marc Nachtergael, Amandine Duez, Pierre Thang, Nguyen Dinh Life (Basel) Article In this study, we showed that crude extract of Anisomeles indica (AI-EtE) expressed its toxicity to HeLa cells with an IC50 dose of 38.8 µg/mL and to zebrafish embryos with malformations, lethality and hatching inhibition at 72-hpf at doses higher than 75 µg/mL. More interestingly, flow cytometry revealed that AI-EtE significantly promoted the number of cells entering apoptotic. Accordingly, the transcript levels of BAX, CASPASE-8, and CASPASE-3 in the cells treated with AI-EtE at IC50 dose were 1.55-, 1.62-, and 2.45-fold higher than those in the control cells, respectively. Moreover, treatment with AI-EtE caused cell cycle arrest at the G1 phase in a p53-independent manner. Particularly, percentages of AI-EtE-treated cells in G1, S, G2/M were, respectively 85%, 6.7% and 6.4%; while percentages of control cells in G1, S, G2/M were 64%, 15% and 19%, respectively. Consistent with cell cycle arrest, the expressions of CDKN1A and CDNK2A in AI-EtE-treated cells were up-regulated 1.9- and 1.64-fold, respectively. Significantly, treatment with AI-EtE also decreased anchorage-independent growth of HeLa cells. In conclusion, we suggest that Anisomeles indica can be considered as a medicinal plant with a possible use against cervical cancer cells; however, the used dose should be carefully monitored, especially when applying to pregnant women. MDPI 2021-03-20 /pmc/articles/PMC8003830/ /pubmed/33804714 http://dx.doi.org/10.3390/life11030257 Text en © 2021 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 (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Bich-Loan, Nguyen T.
Kien, Kieu Trung
Thanh, Nguyen Lai
Kim-Thanh, Nguyen T.
Huy, Nguyen Quang
The-Hai, Pham
Muller, Marc
Nachtergael, Amandine
Duez, Pierre
Thang, Nguyen Dinh
Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos
title Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos
title_full Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos
title_fullStr Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos
title_full_unstemmed Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos
title_short Toxicity and Anti-Proliferative Properties of Anisomeles indica Ethanol Extract on Cervical Cancer HeLa Cells and Zebrafish Embryos
title_sort toxicity and anti-proliferative properties of anisomeles indica ethanol extract on cervical cancer hela cells and zebrafish embryos
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8003830/
https://www.ncbi.nlm.nih.gov/pubmed/33804714
http://dx.doi.org/10.3390/life11030257
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