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Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma
Melanoma, the most serious yet uncommon type of cancer, originates in melanocytes. Risk factors include UV radiation, genetic factors, tanning lamps and beds. Here, we described the synthesis and selective anti melanoma activity of [3,2-b]indole fused 18β-glycyrrhetinic acid, a derivative of 18β-gly...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086573/ https://www.ncbi.nlm.nih.gov/pubmed/37056972 http://dx.doi.org/10.1039/d2ra08023k |
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author | Kumar, Amit Gupta, Ragni Rashid, Haroon Bhat, Aalim Maqsood Sharma, Raghu Rai Naikoo, Shahid Hussain Kaur, Sarabjit Tasduq, Sheikh Abdullah |
author_facet | Kumar, Amit Gupta, Ragni Rashid, Haroon Bhat, Aalim Maqsood Sharma, Raghu Rai Naikoo, Shahid Hussain Kaur, Sarabjit Tasduq, Sheikh Abdullah |
author_sort | Kumar, Amit |
collection | PubMed |
description | Melanoma, the most serious yet uncommon type of cancer, originates in melanocytes. Risk factors include UV radiation, genetic factors, tanning lamps and beds. Here, we described the synthesis and selective anti melanoma activity of [3,2-b]indole fused 18β-glycyrrhetinic acid, a derivative of 18β-glycyrrhetinic acid in murine B16F10 and A375 human melanoma cell lines. Among the 14 molecules, GPD-12 showed significant selective cytotoxic activity against A375 and B16F10 cell lines with IC50 of 13.38 μM and 15.20 μM respectively. GPD 12 induced the formation of reactive oxygen species in A375 cells that could trigger oxidative stress mediated cell death as is evident from the increased expression of apoptosis related proteins such as caspase-9 and caspase-3 and the increased ratio of Bax to Bcl2. The results showed that GPD 12 can be used as an effective therapeutic agent against melanoma. |
format | Online Article Text |
id | pubmed-10086573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-100865732023-04-12 Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma Kumar, Amit Gupta, Ragni Rashid, Haroon Bhat, Aalim Maqsood Sharma, Raghu Rai Naikoo, Shahid Hussain Kaur, Sarabjit Tasduq, Sheikh Abdullah RSC Adv Chemistry Melanoma, the most serious yet uncommon type of cancer, originates in melanocytes. Risk factors include UV radiation, genetic factors, tanning lamps and beds. Here, we described the synthesis and selective anti melanoma activity of [3,2-b]indole fused 18β-glycyrrhetinic acid, a derivative of 18β-glycyrrhetinic acid in murine B16F10 and A375 human melanoma cell lines. Among the 14 molecules, GPD-12 showed significant selective cytotoxic activity against A375 and B16F10 cell lines with IC50 of 13.38 μM and 15.20 μM respectively. GPD 12 induced the formation of reactive oxygen species in A375 cells that could trigger oxidative stress mediated cell death as is evident from the increased expression of apoptosis related proteins such as caspase-9 and caspase-3 and the increased ratio of Bax to Bcl2. The results showed that GPD 12 can be used as an effective therapeutic agent against melanoma. The Royal Society of Chemistry 2023-04-11 /pmc/articles/PMC10086573/ /pubmed/37056972 http://dx.doi.org/10.1039/d2ra08023k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Kumar, Amit Gupta, Ragni Rashid, Haroon Bhat, Aalim Maqsood Sharma, Raghu Rai Naikoo, Shahid Hussain Kaur, Sarabjit Tasduq, Sheikh Abdullah Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma |
title | Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma |
title_full | Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma |
title_fullStr | Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma |
title_full_unstemmed | Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma |
title_short | Synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma |
title_sort | synthesis, molecular docking, and biological evaluation of [3,2-b]indole fused 18β-glycyrrhetinic acid derivatives against skin melanoma |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086573/ https://www.ncbi.nlm.nih.gov/pubmed/37056972 http://dx.doi.org/10.1039/d2ra08023k |
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