The University of Southampton
University of Southampton Institutional Repository

Oncogenic protein tyrosine kinases: Oncogenic derivatives of platelet-derived growth factor receptors

Oncogenic protein tyrosine kinases: Oncogenic derivatives of platelet-derived growth factor receptors
Oncogenic protein tyrosine kinases: Oncogenic derivatives of platelet-derived growth factor receptors
Platelet-derived growth factor receptors (PDGFRs) and their ligands, platelet-derived growth factors (PDGFs) play critical roles in mesenchymal cell migration and proliferation. In embryogenesis the PDGFR/PDGF system is essential for the correct development of the kidney, cardiovascular system, brain, lung and connective tissue. In adults, PDGFR/PDGF is important in wound healing, inflammation and angiogenesis. Abnormalities of PDGFR/PDGF are thought to contribute to a number of human diseases, and especially malignancy. Constitutive activation of the PDGFR? or PDGFR? receptor tyrosine kinases is seen in myeloid malignancies as a consequence of fusion to diverse partner genes, and activating mutations of PDGFR? are seen in gastrointestinal tumours (GISTs). Autocrine signalling as a consequence of PDGF-B overexpression is clearly implicated in the pathogenesis of dermatofibrosarcoma protruberans (DFSP) and overexpression of PDGFRs and/or their ligands has been described in many solid tumours. PDGFR signalling is inhibited by imatinib mesylate, and this compound has clear clinical activity in patients with myeloid malignancies, GIST and DFSP.
pdgfra, pdgfrb, imatinib
1420-682X
2912-2923
Jones, A.V.
daa5d0cf-4454-48c3-abb8-daf03aa21e8b
Cross, N.C.P.
f87650da-b908-4a34-b31b-d62c5f186fe4
Jones, A.V.
daa5d0cf-4454-48c3-abb8-daf03aa21e8b
Cross, N.C.P.
f87650da-b908-4a34-b31b-d62c5f186fe4

Jones, A.V. and Cross, N.C.P. (2004) Oncogenic protein tyrosine kinases: Oncogenic derivatives of platelet-derived growth factor receptors. Cellular and Molecular Life Sciences, 61 (23), 2912-2923. (doi:10.1007/s00018-004-4272-z).

Record type: Article

Abstract

Platelet-derived growth factor receptors (PDGFRs) and their ligands, platelet-derived growth factors (PDGFs) play critical roles in mesenchymal cell migration and proliferation. In embryogenesis the PDGFR/PDGF system is essential for the correct development of the kidney, cardiovascular system, brain, lung and connective tissue. In adults, PDGFR/PDGF is important in wound healing, inflammation and angiogenesis. Abnormalities of PDGFR/PDGF are thought to contribute to a number of human diseases, and especially malignancy. Constitutive activation of the PDGFR? or PDGFR? receptor tyrosine kinases is seen in myeloid malignancies as a consequence of fusion to diverse partner genes, and activating mutations of PDGFR? are seen in gastrointestinal tumours (GISTs). Autocrine signalling as a consequence of PDGF-B overexpression is clearly implicated in the pathogenesis of dermatofibrosarcoma protruberans (DFSP) and overexpression of PDGFRs and/or their ligands has been described in many solid tumours. PDGFR signalling is inhibited by imatinib mesylate, and this compound has clear clinical activity in patients with myeloid malignancies, GIST and DFSP.

This record has no associated files available for download.

More information

Published date: 2004
Keywords: pdgfra, pdgfrb, imatinib

Identifiers

Local EPrints ID: 24783
URI: http://eprints.soton.ac.uk/id/eprint/24783
ISSN: 1420-682X
PURE UUID: f50b318b-ef8f-45a1-875d-297e6fee432f
ORCID for N.C.P. Cross: ORCID iD orcid.org/0000-0001-5481-2555

Catalogue record

Date deposited: 03 Apr 2006
Last modified: 16 Mar 2024 03:23

Export record

Altmetrics

Contributors

Author: A.V. Jones
Author: N.C.P. Cross ORCID iD

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×