Pharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling

The ubiquitin-proteasome pathway (UPP) is involved in regulating several biological functions, including cell cycle control, apoptosis, DNA damage response, and apoptosis. It is widely known for its role in degrading abnormal protein substrates and maintaining physiological body functions via ubiqui...

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Autores principales: Anmol Sharma, Heena Khan, Thakur Gurjeet Singh, Amarjot Kaur Grewal, Agnieszka Najda, Małgorzata Kawecka-Radomska, Mohamed Kamel, Ahmed E. Altyar, Mohamed M. del-Daim
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/e74f7df8c33d48aa9c759e1e249f9b75
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spelling oai:doaj.org-article:e74f7df8c33d48aa9c759e1e249f9b752021-11-11T17:23:34ZPharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling10.3390/ijms2221119711422-00671661-6596https://doaj.org/article/e74f7df8c33d48aa9c759e1e249f9b752021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/21/11971https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067The ubiquitin-proteasome pathway (UPP) is involved in regulating several biological functions, including cell cycle control, apoptosis, DNA damage response, and apoptosis. It is widely known for its role in degrading abnormal protein substrates and maintaining physiological body functions via ubiquitinating enzymes (E1, E2, E3) and the proteasome. Therefore, aberrant expression in these enzymes results in an altered biological process, including transduction signaling for cell death and survival, resulting in cancer. In this review, an overview of profuse enzymes involved as a pro-oncogenic or progressive growth factor in tumors with their downstream signaling pathways has been discussed. A systematic literature review of PubMed, Medline, Bentham, Scopus, and EMBASE (Elsevier) databases was carried out to understand the nature of the extensive work done on modulation of ubiquitin-proteasome pathways in oncogenic signaling. Various in vitro, in vivo studies demonstrating the involvement of ubiquitin-proteasome systems in varied types of cancers and the downstream signaling pathways involved are also discussed in the current review. Several inhibitors of E1, E2, E3, deubiquitinase enzymes and proteasome have been applied for treating cancer. Some of these drugs have exhibited successful outcomes in in vivo studies on different cancer types, so clinical trials are going on for these inhibitors. This review mainly focuses on certain ubiquitin-proteasome enzymes involved in developing cancers and certain enzymes that can be targeted to treat cancer.Anmol SharmaHeena KhanThakur Gurjeet SinghAmarjot Kaur GrewalAgnieszka NajdaMałgorzata Kawecka-RadomskaMohamed KamelAhmed E. AltyarMohamed M. del-DaimMDPI AGarticlecancerubiquitinationubiquitin-proteasome systemdeubiquitinationubiquitin inhibitorsBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 11971, p 11971 (2021)
institution DOAJ
collection DOAJ
language EN
topic cancer
ubiquitination
ubiquitin-proteasome system
deubiquitination
ubiquitin inhibitors
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle cancer
ubiquitination
ubiquitin-proteasome system
deubiquitination
ubiquitin inhibitors
Biology (General)
QH301-705.5
Chemistry
QD1-999
Anmol Sharma
Heena Khan
Thakur Gurjeet Singh
Amarjot Kaur Grewal
Agnieszka Najda
Małgorzata Kawecka-Radomska
Mohamed Kamel
Ahmed E. Altyar
Mohamed M. del-Daim
Pharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling
description The ubiquitin-proteasome pathway (UPP) is involved in regulating several biological functions, including cell cycle control, apoptosis, DNA damage response, and apoptosis. It is widely known for its role in degrading abnormal protein substrates and maintaining physiological body functions via ubiquitinating enzymes (E1, E2, E3) and the proteasome. Therefore, aberrant expression in these enzymes results in an altered biological process, including transduction signaling for cell death and survival, resulting in cancer. In this review, an overview of profuse enzymes involved as a pro-oncogenic or progressive growth factor in tumors with their downstream signaling pathways has been discussed. A systematic literature review of PubMed, Medline, Bentham, Scopus, and EMBASE (Elsevier) databases was carried out to understand the nature of the extensive work done on modulation of ubiquitin-proteasome pathways in oncogenic signaling. Various in vitro, in vivo studies demonstrating the involvement of ubiquitin-proteasome systems in varied types of cancers and the downstream signaling pathways involved are also discussed in the current review. Several inhibitors of E1, E2, E3, deubiquitinase enzymes and proteasome have been applied for treating cancer. Some of these drugs have exhibited successful outcomes in in vivo studies on different cancer types, so clinical trials are going on for these inhibitors. This review mainly focuses on certain ubiquitin-proteasome enzymes involved in developing cancers and certain enzymes that can be targeted to treat cancer.
format article
author Anmol Sharma
Heena Khan
Thakur Gurjeet Singh
Amarjot Kaur Grewal
Agnieszka Najda
Małgorzata Kawecka-Radomska
Mohamed Kamel
Ahmed E. Altyar
Mohamed M. del-Daim
author_facet Anmol Sharma
Heena Khan
Thakur Gurjeet Singh
Amarjot Kaur Grewal
Agnieszka Najda
Małgorzata Kawecka-Radomska
Mohamed Kamel
Ahmed E. Altyar
Mohamed M. del-Daim
author_sort Anmol Sharma
title Pharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling
title_short Pharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling
title_full Pharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling
title_fullStr Pharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling
title_full_unstemmed Pharmacological Modulation of Ubiquitin-Proteasome Pathways in Oncogenic Signaling
title_sort pharmacological modulation of ubiquitin-proteasome pathways in oncogenic signaling
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/e74f7df8c33d48aa9c759e1e249f9b75
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