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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...

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Autores principales: Kumar, Amit, Gupta, Ragni, Rashid, Haroon, Bhat, Aalim Maqsood, Sharma, Raghu Rai, Naikoo, Shahid Hussain, Kaur, Sarabjit, Tasduq, Sheikh Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
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.
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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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