Cargando…

Protein Tyrosine Phosphatases: Mechanisms in Cancer

Protein tyrosine kinases, especially receptor tyrosine kinases, have dominated the cancer therapeutics sphere as proteins that can be inhibited to selectively target cancer. However, protein tyrosine phosphatases (PTPs) are also an emerging target. Though historically known as negative regulators of...

Descripción completa

Detalles Bibliográficos
Autores principales: Sivaganesh, Vignesh, Sivaganesh, Varsha, Scanlon, Christina, Iskander, Alexander, Maher, Salma, Lê, Thư, Peethambaran, Bela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8657787/
https://www.ncbi.nlm.nih.gov/pubmed/34884670
http://dx.doi.org/10.3390/ijms222312865
_version_ 1784612582360875008
author Sivaganesh, Vignesh
Sivaganesh, Varsha
Scanlon, Christina
Iskander, Alexander
Maher, Salma
Lê, Thư
Peethambaran, Bela
author_facet Sivaganesh, Vignesh
Sivaganesh, Varsha
Scanlon, Christina
Iskander, Alexander
Maher, Salma
Lê, Thư
Peethambaran, Bela
author_sort Sivaganesh, Vignesh
collection PubMed
description Protein tyrosine kinases, especially receptor tyrosine kinases, have dominated the cancer therapeutics sphere as proteins that can be inhibited to selectively target cancer. However, protein tyrosine phosphatases (PTPs) are also an emerging target. Though historically known as negative regulators of the oncogenic tyrosine kinases, PTPs are now known to be both tumor-suppressive and oncogenic. This review will highlight key protein tyrosine phosphatases that have been thoroughly investigated in various cancers. Furthermore, the different mechanisms underlying pro-cancerous and anti-cancerous PTPs will also be explored.
format Online
Article
Text
id pubmed-8657787
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86577872021-12-10 Protein Tyrosine Phosphatases: Mechanisms in Cancer Sivaganesh, Vignesh Sivaganesh, Varsha Scanlon, Christina Iskander, Alexander Maher, Salma Lê, Thư Peethambaran, Bela Int J Mol Sci Review Protein tyrosine kinases, especially receptor tyrosine kinases, have dominated the cancer therapeutics sphere as proteins that can be inhibited to selectively target cancer. However, protein tyrosine phosphatases (PTPs) are also an emerging target. Though historically known as negative regulators of the oncogenic tyrosine kinases, PTPs are now known to be both tumor-suppressive and oncogenic. This review will highlight key protein tyrosine phosphatases that have been thoroughly investigated in various cancers. Furthermore, the different mechanisms underlying pro-cancerous and anti-cancerous PTPs will also be explored. MDPI 2021-11-28 /pmc/articles/PMC8657787/ /pubmed/34884670 http://dx.doi.org/10.3390/ijms222312865 Text en © 2021 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
Sivaganesh, Vignesh
Sivaganesh, Varsha
Scanlon, Christina
Iskander, Alexander
Maher, Salma
Lê, Thư
Peethambaran, Bela
Protein Tyrosine Phosphatases: Mechanisms in Cancer
title Protein Tyrosine Phosphatases: Mechanisms in Cancer
title_full Protein Tyrosine Phosphatases: Mechanisms in Cancer
title_fullStr Protein Tyrosine Phosphatases: Mechanisms in Cancer
title_full_unstemmed Protein Tyrosine Phosphatases: Mechanisms in Cancer
title_short Protein Tyrosine Phosphatases: Mechanisms in Cancer
title_sort protein tyrosine phosphatases: mechanisms in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8657787/
https://www.ncbi.nlm.nih.gov/pubmed/34884670
http://dx.doi.org/10.3390/ijms222312865
work_keys_str_mv AT sivaganeshvignesh proteintyrosinephosphatasesmechanismsincancer
AT sivaganeshvarsha proteintyrosinephosphatasesmechanismsincancer
AT scanlonchristina proteintyrosinephosphatasesmechanismsincancer
AT iskanderalexander proteintyrosinephosphatasesmechanismsincancer
AT mahersalma proteintyrosinephosphatasesmechanismsincancer
AT lethu proteintyrosinephosphatasesmechanismsincancer
AT peethambaranbela proteintyrosinephosphatasesmechanismsincancer