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Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling

Triacontanoic ester of 5ʺ-hydroxyjustisolin, a lignan from Justicia simplex D. Don, possesses antitumor activity. However, the molecular mechanism underlying this is not yet clearly understood. The present study showed significant inhibition in cell viability on HeLa cell line and induced minor toxi...

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Detalles Bibliográficos
Autores principales: Joseph, Litty, Srinivasan, K.K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872787/
https://www.ncbi.nlm.nih.gov/pubmed/31768331
http://dx.doi.org/10.1016/j.toxrep.2019.10.015
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author Joseph, Litty
Srinivasan, K.K.
author_facet Joseph, Litty
Srinivasan, K.K.
author_sort Joseph, Litty
collection PubMed
description Triacontanoic ester of 5ʺ-hydroxyjustisolin, a lignan from Justicia simplex D. Don, possesses antitumor activity. However, the molecular mechanism underlying this is not yet clearly understood. The present study showed significant inhibition in cell viability on HeLa cell line and induced minor toxicity in normal cells. This compound induced mitotic arrest at G0/G1 phase followed by apoptosis in human cervical cancer cells and was accompanied by the upregulation of BAX, caspase-3 and downregulation of Bcl-2. Taken together, these data reveal that the title compound acts through multiple cellular/molecular pathways, which strongly suggest the role of pro and antiapoptotic Bcl-2 family proteins. Triacontanoic ester of 5ʹʹ-hydroxyjustisolin may be a potential agent for the cervical cancer treatment.
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spelling pubmed-68727872019-11-25 Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling Joseph, Litty Srinivasan, K.K. Toxicol Rep Article Triacontanoic ester of 5ʺ-hydroxyjustisolin, a lignan from Justicia simplex D. Don, possesses antitumor activity. However, the molecular mechanism underlying this is not yet clearly understood. The present study showed significant inhibition in cell viability on HeLa cell line and induced minor toxicity in normal cells. This compound induced mitotic arrest at G0/G1 phase followed by apoptosis in human cervical cancer cells and was accompanied by the upregulation of BAX, caspase-3 and downregulation of Bcl-2. Taken together, these data reveal that the title compound acts through multiple cellular/molecular pathways, which strongly suggest the role of pro and antiapoptotic Bcl-2 family proteins. Triacontanoic ester of 5ʹʹ-hydroxyjustisolin may be a potential agent for the cervical cancer treatment. Elsevier 2019-10-31 /pmc/articles/PMC6872787/ /pubmed/31768331 http://dx.doi.org/10.1016/j.toxrep.2019.10.015 Text en © 2019 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Joseph, Litty
Srinivasan, K.K.
Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling
title Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling
title_full Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling
title_fullStr Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling
title_full_unstemmed Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling
title_short Triacontanoic ester of 5ʹʹ-hydroxyjustisolin: Tumour suppressive role in cervical cancer via Bcl-2, BAX and caspase-3 mediated signalling
title_sort triacontanoic ester of 5ʹʹ-hydroxyjustisolin: tumour suppressive role in cervical cancer via bcl-2, bax and caspase-3 mediated signalling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872787/
https://www.ncbi.nlm.nih.gov/pubmed/31768331
http://dx.doi.org/10.1016/j.toxrep.2019.10.015
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