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Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC

Withaferin A, a steroidal lactone derived from the Withania somnifera plant has been known for its anti-cancerous effects on various types of cancer cells. However, its effect on the hallmarks of cancer such as proliferation, migration, invasion, and angiogenesis is still poorly understood. The anti...

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Autores principales: Shiragannavar, Varsha D., Gowda, Nirmala G. Sannappa, Kumar, Divya P., Mirshahi, Faridoddin, Santhekadur, Prasanna K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878559/
https://www.ncbi.nlm.nih.gov/pubmed/33585254
http://dx.doi.org/10.3389/fonc.2020.628506
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author Shiragannavar, Varsha D.
Gowda, Nirmala G. Sannappa
Kumar, Divya P.
Mirshahi, Faridoddin
Santhekadur, Prasanna K.
author_facet Shiragannavar, Varsha D.
Gowda, Nirmala G. Sannappa
Kumar, Divya P.
Mirshahi, Faridoddin
Santhekadur, Prasanna K.
author_sort Shiragannavar, Varsha D.
collection PubMed
description Withaferin A, a steroidal lactone derived from the Withania somnifera plant has been known for its anti-cancerous effects on various types of cancer cells. However, its effect on the hallmarks of cancer such as proliferation, migration, invasion, and angiogenesis is still poorly understood. The antitumor property of Withaferin A and its molecular mechanism of action on hepatocellular carcinoma (HCC) cells is not yet completely established. In this study, we aimed to elucidate the novel molecular function of Withaferin A on HCC cells and its effect on various gene expression. Our results clearly showed that Withaferin A treatment to HCC cells inhibited proliferation, migration, invasion, and anchorage-independent growth. Further, we explored the Withaferin A target genes by blotting human angiogenesis, and cytokine arrays using conditioned media of Withaferin A treated QGY-7703 cells. We found that many of Nuclear factor kappa B (NF-κB), angiogenesis and inflammation associated proteins secretion is downregulated upon Withaferin A treatment. Interestingly, all these genes expression is also negatively regulated by nuclear receptor Liver X receptor-α (LXR-α). Here, we explored a novel mechanism that Withaferin-A activated LXR-α inhibits NF-κB transcriptional activity and suppressed the proliferation, migration, invasion, and anchorage-independent growth of these HCC cells. All these data strongly confirmed that Withaferin A is a potent anticancer compound and suppresses various angiogenesis and inflammatory markers which are associated with the development and progression of HCC. This beneficial and potential therapeutic property of Withaferin A will be very useful for the treatment of HCC.
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spelling pubmed-78785592021-02-13 Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC Shiragannavar, Varsha D. Gowda, Nirmala G. Sannappa Kumar, Divya P. Mirshahi, Faridoddin Santhekadur, Prasanna K. Front Oncol Oncology Withaferin A, a steroidal lactone derived from the Withania somnifera plant has been known for its anti-cancerous effects on various types of cancer cells. However, its effect on the hallmarks of cancer such as proliferation, migration, invasion, and angiogenesis is still poorly understood. The antitumor property of Withaferin A and its molecular mechanism of action on hepatocellular carcinoma (HCC) cells is not yet completely established. In this study, we aimed to elucidate the novel molecular function of Withaferin A on HCC cells and its effect on various gene expression. Our results clearly showed that Withaferin A treatment to HCC cells inhibited proliferation, migration, invasion, and anchorage-independent growth. Further, we explored the Withaferin A target genes by blotting human angiogenesis, and cytokine arrays using conditioned media of Withaferin A treated QGY-7703 cells. We found that many of Nuclear factor kappa B (NF-κB), angiogenesis and inflammation associated proteins secretion is downregulated upon Withaferin A treatment. Interestingly, all these genes expression is also negatively regulated by nuclear receptor Liver X receptor-α (LXR-α). Here, we explored a novel mechanism that Withaferin-A activated LXR-α inhibits NF-κB transcriptional activity and suppressed the proliferation, migration, invasion, and anchorage-independent growth of these HCC cells. All these data strongly confirmed that Withaferin A is a potent anticancer compound and suppresses various angiogenesis and inflammatory markers which are associated with the development and progression of HCC. This beneficial and potential therapeutic property of Withaferin A will be very useful for the treatment of HCC. Frontiers Media S.A. 2021-01-29 /pmc/articles/PMC7878559/ /pubmed/33585254 http://dx.doi.org/10.3389/fonc.2020.628506 Text en Copyright © 2021 Shiragannavar, Gowda, Kumar, Mirshahi and Santhekadur http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Shiragannavar, Varsha D.
Gowda, Nirmala G. Sannappa
Kumar, Divya P.
Mirshahi, Faridoddin
Santhekadur, Prasanna K.
Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC
title Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC
title_full Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC
title_fullStr Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC
title_full_unstemmed Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC
title_short Withaferin A Acts as a Novel Regulator of Liver X Receptor-α in HCC
title_sort withaferin a acts as a novel regulator of liver x receptor-α in hcc
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878559/
https://www.ncbi.nlm.nih.gov/pubmed/33585254
http://dx.doi.org/10.3389/fonc.2020.628506
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