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Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics

Homeostasis between protein synthesis and degradation is a critical biological function involving a lot of precise and intricate regulatory systems. The ubiquitin-proteasome pathway (UPP) is a large, multi-protease complex that degrades most intracellular proteins and accounts for about 80% of cellu...

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Autores principales: Mir, Reyaz Hassan, Mir, Prince Ahad, Uppal, Jasreen, Chawla, Apporva, Patel, Mitesh, Bardakci, Fevzi, Adnan, Mohd, Mohi-ud-din, Roohi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142660/
https://www.ncbi.nlm.nih.gov/pubmed/37110167
http://dx.doi.org/10.3390/metabo13040509
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author Mir, Reyaz Hassan
Mir, Prince Ahad
Uppal, Jasreen
Chawla, Apporva
Patel, Mitesh
Bardakci, Fevzi
Adnan, Mohd
Mohi-ud-din, Roohi
author_facet Mir, Reyaz Hassan
Mir, Prince Ahad
Uppal, Jasreen
Chawla, Apporva
Patel, Mitesh
Bardakci, Fevzi
Adnan, Mohd
Mohi-ud-din, Roohi
author_sort Mir, Reyaz Hassan
collection PubMed
description Homeostasis between protein synthesis and degradation is a critical biological function involving a lot of precise and intricate regulatory systems. The ubiquitin-proteasome pathway (UPP) is a large, multi-protease complex that degrades most intracellular proteins and accounts for about 80% of cellular protein degradation. The proteasome, a massive multi-catalytic proteinase complex that plays a substantial role in protein processing, has been shown to have a wide range of catalytic activity and is at the center of this eukaryotic protein breakdown mechanism. As cancer cells overexpress proteins that induce cell proliferation, while blocking cell death pathways, UPP inhibition has been used as an anticancer therapy to change the balance between protein production and degradation towards cell death. Natural products have a long history of being used to prevent and treat various illnesses. Modern research has shown that the pharmacological actions of several natural products are involved in the engagement of UPP. Over the past few years, numerous natural compounds have been found that target the UPP pathway. These molecules could lead to the clinical development of novel and potent anticancer medications to combat the onslaught of adverse effects and resistance mechanisms caused by already approved proteasome inhibitors. In this review, we report the importance of UPP in anticancer therapy and the regulatory effects of diverse natural metabolites, their semi-synthetic analogs, and SAR studies on proteasome components, which may aid in discovering a new proteasome regulator for drug development and clinical applications.
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spelling pubmed-101426602023-04-29 Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics Mir, Reyaz Hassan Mir, Prince Ahad Uppal, Jasreen Chawla, Apporva Patel, Mitesh Bardakci, Fevzi Adnan, Mohd Mohi-ud-din, Roohi Metabolites Review Homeostasis between protein synthesis and degradation is a critical biological function involving a lot of precise and intricate regulatory systems. The ubiquitin-proteasome pathway (UPP) is a large, multi-protease complex that degrades most intracellular proteins and accounts for about 80% of cellular protein degradation. The proteasome, a massive multi-catalytic proteinase complex that plays a substantial role in protein processing, has been shown to have a wide range of catalytic activity and is at the center of this eukaryotic protein breakdown mechanism. As cancer cells overexpress proteins that induce cell proliferation, while blocking cell death pathways, UPP inhibition has been used as an anticancer therapy to change the balance between protein production and degradation towards cell death. Natural products have a long history of being used to prevent and treat various illnesses. Modern research has shown that the pharmacological actions of several natural products are involved in the engagement of UPP. Over the past few years, numerous natural compounds have been found that target the UPP pathway. These molecules could lead to the clinical development of novel and potent anticancer medications to combat the onslaught of adverse effects and resistance mechanisms caused by already approved proteasome inhibitors. In this review, we report the importance of UPP in anticancer therapy and the regulatory effects of diverse natural metabolites, their semi-synthetic analogs, and SAR studies on proteasome components, which may aid in discovering a new proteasome regulator for drug development and clinical applications. MDPI 2023-03-31 /pmc/articles/PMC10142660/ /pubmed/37110167 http://dx.doi.org/10.3390/metabo13040509 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mir, Reyaz Hassan
Mir, Prince Ahad
Uppal, Jasreen
Chawla, Apporva
Patel, Mitesh
Bardakci, Fevzi
Adnan, Mohd
Mohi-ud-din, Roohi
Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics
title Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics
title_full Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics
title_fullStr Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics
title_full_unstemmed Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics
title_short Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics
title_sort evolution of natural product scaffolds as potential proteasome inhibitors in developing cancer therapeutics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142660/
https://www.ncbi.nlm.nih.gov/pubmed/37110167
http://dx.doi.org/10.3390/metabo13040509
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