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Antiproliferative Potential of Gloriosine: A Lead for Anticancer Drug Development
[Image: see text] Gloriosine, a colchicine-like natural product, is widely obtained from Gloriosa superba roots. Despite having remarkable anticancer potential, colchicine could not pave its way to the clinic, while gloriosine is yet to be investigated for its pharmacological effects. In the present...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404168/ https://www.ncbi.nlm.nih.gov/pubmed/36033689 http://dx.doi.org/10.1021/acsomega.2c02688 |
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author | Goel, Bharat Dey, Biswajit Chatterjee, Essha Tripathi, Nancy Bhardwaj, Nivedita Kumar, Sanjay Guru, Santosh Kumar Jain, Shreyans K. |
author_facet | Goel, Bharat Dey, Biswajit Chatterjee, Essha Tripathi, Nancy Bhardwaj, Nivedita Kumar, Sanjay Guru, Santosh Kumar Jain, Shreyans K. |
author_sort | Goel, Bharat |
collection | PubMed |
description | [Image: see text] Gloriosine, a colchicine-like natural product, is widely obtained from Gloriosa superba roots. Despite having remarkable anticancer potential, colchicine could not pave its way to the clinic, while gloriosine is yet to be investigated for its pharmacological effects. In the present work, 14 compounds, including gloriosine, were isolated from the G. superba roots and were characterized by NMR spectroscopy. Gloriosine (11) was evaluated for its antiproliferative activity against a panel of 15 human cancer cell lines of different tissues and normal breast cells. Gloroisine (11) displayed significant antiproliferative activity against various cancer cell lines selectively, with IC(50) values ranging from 32.61 to 100.28 nM. Further, gloriosine (11) was investigated for its apoptosis-inducing ability and found to form apoptotic bodies. It also inhibited A549 cell migration in the wound healing assay. Finally, molecular docking studies were performed to explore the possible binding modes of gloriosine with the colchicine-binding site of tubulin protein. Our findings suggested that gloriosine might be a potential lead for anticancer drug discovery. |
format | Online Article Text |
id | pubmed-9404168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94041682022-08-26 Antiproliferative Potential of Gloriosine: A Lead for Anticancer Drug Development Goel, Bharat Dey, Biswajit Chatterjee, Essha Tripathi, Nancy Bhardwaj, Nivedita Kumar, Sanjay Guru, Santosh Kumar Jain, Shreyans K. ACS Omega [Image: see text] Gloriosine, a colchicine-like natural product, is widely obtained from Gloriosa superba roots. Despite having remarkable anticancer potential, colchicine could not pave its way to the clinic, while gloriosine is yet to be investigated for its pharmacological effects. In the present work, 14 compounds, including gloriosine, were isolated from the G. superba roots and were characterized by NMR spectroscopy. Gloriosine (11) was evaluated for its antiproliferative activity against a panel of 15 human cancer cell lines of different tissues and normal breast cells. Gloroisine (11) displayed significant antiproliferative activity against various cancer cell lines selectively, with IC(50) values ranging from 32.61 to 100.28 nM. Further, gloriosine (11) was investigated for its apoptosis-inducing ability and found to form apoptotic bodies. It also inhibited A549 cell migration in the wound healing assay. Finally, molecular docking studies were performed to explore the possible binding modes of gloriosine with the colchicine-binding site of tubulin protein. Our findings suggested that gloriosine might be a potential lead for anticancer drug discovery. American Chemical Society 2022-08-12 /pmc/articles/PMC9404168/ /pubmed/36033689 http://dx.doi.org/10.1021/acsomega.2c02688 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Goel, Bharat Dey, Biswajit Chatterjee, Essha Tripathi, Nancy Bhardwaj, Nivedita Kumar, Sanjay Guru, Santosh Kumar Jain, Shreyans K. Antiproliferative Potential of Gloriosine: A Lead for Anticancer Drug Development |
title | Antiproliferative
Potential of Gloriosine: A Lead
for Anticancer Drug Development |
title_full | Antiproliferative
Potential of Gloriosine: A Lead
for Anticancer Drug Development |
title_fullStr | Antiproliferative
Potential of Gloriosine: A Lead
for Anticancer Drug Development |
title_full_unstemmed | Antiproliferative
Potential of Gloriosine: A Lead
for Anticancer Drug Development |
title_short | Antiproliferative
Potential of Gloriosine: A Lead
for Anticancer Drug Development |
title_sort | antiproliferative
potential of gloriosine: a lead
for anticancer drug development |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404168/ https://www.ncbi.nlm.nih.gov/pubmed/36033689 http://dx.doi.org/10.1021/acsomega.2c02688 |
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