Cargando…

Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes

Tyrosine kinase inhibitors (TKIs) have been studied extensively in cancer research, ultimately resulting in the approval of many drugs for cancer therapy. Recent evidence from reported clinical cases and experimental studies have suggested that some of these drugs have a potential role in diabetes t...

Descripción completa

Detalles Bibliográficos
Autor principal: Althubiti, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555044/
https://www.ncbi.nlm.nih.gov/pubmed/36247049
http://dx.doi.org/10.4103/sjmms.sjmms_492_21
_version_ 1784806828842942464
author Althubiti, Mohammad
author_facet Althubiti, Mohammad
author_sort Althubiti, Mohammad
collection PubMed
description Tyrosine kinase inhibitors (TKIs) have been studied extensively in cancer research, ultimately resulting in the approval of many drugs for cancer therapy. Recent evidence from reported clinical cases and experimental studies have suggested that some of these drugs have a potential role in diabetes treatment. These TKIs include imatinib, sunitinib, dasatinib, erlotinib, nilotinib, neratinib, and ibrutinib. As a result of promising findings, imatinib has been used in a phase II clinical trial. In this review, studies that used TKIs in the treatment of both types of diabetes are critically discussed. In addition, the different molecular mechanisms of action of these drugs in diabetes models are also highlighted to understand their antidiabetic mode of action.
format Online
Article
Text
id pubmed-9555044
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-95550442022-10-13 Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes Althubiti, Mohammad Saudi J Med Med Sci Review Article Tyrosine kinase inhibitors (TKIs) have been studied extensively in cancer research, ultimately resulting in the approval of many drugs for cancer therapy. Recent evidence from reported clinical cases and experimental studies have suggested that some of these drugs have a potential role in diabetes treatment. These TKIs include imatinib, sunitinib, dasatinib, erlotinib, nilotinib, neratinib, and ibrutinib. As a result of promising findings, imatinib has been used in a phase II clinical trial. In this review, studies that used TKIs in the treatment of both types of diabetes are critically discussed. In addition, the different molecular mechanisms of action of these drugs in diabetes models are also highlighted to understand their antidiabetic mode of action. Wolters Kluwer - Medknow 2022 2022-09-07 /pmc/articles/PMC9555044/ /pubmed/36247049 http://dx.doi.org/10.4103/sjmms.sjmms_492_21 Text en Copyright: © 2022 Saudi Journal of Medicine & Medical Sciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Althubiti, Mohammad
Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes
title Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes
title_full Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes
title_fullStr Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes
title_full_unstemmed Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes
title_short Tyrosine Kinase Targeting: A Potential Therapeutic Strategy for Diabetes
title_sort tyrosine kinase targeting: a potential therapeutic strategy for diabetes
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555044/
https://www.ncbi.nlm.nih.gov/pubmed/36247049
http://dx.doi.org/10.4103/sjmms.sjmms_492_21
work_keys_str_mv AT althubitimohammad tyrosinekinasetargetingapotentialtherapeuticstrategyfordiabetes