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dc.contributor.authorBoard, Ruth E
dc.contributor.authorJayson, Gordon C
dc.date.accessioned2009-07-29T12:22:33Z
dc.date.available2009-07-29T12:22:33Z
dc.date.issued2005
dc.identifier.citationPlatelet-derived growth factor receptor (PDGFR): a target for anticancer therapeutics., 8 (1-2):75-83 Drug Resist. Updat.en
dc.identifier.issn1368-7646
dc.identifier.pmid15939344
dc.identifier.doi10.1016/j.drup.2005.03.004
dc.identifier.urihttp://hdl.handle.net/10541/75839
dc.description.abstractPlatelet-derived growth factors (PDGFs) and their tyrosine kinase receptors (PDGFRs) have been implicated in the pathogenesis of a number of tumor types and play an important role in angiogenesis. Tumor growth can be promoted by PDGF via autocrine stimulation of malignant cells, by overexpression or overactivation of PDGFRs, or by stimulation of angiogenesis within the tumor. These mechanisms could provide possible therapeutic targets. PDGFR blockade may also lower the interstitial fluid pressure within solid tumors and enhance drug delivery. Here we discuss the possible therapeutic roles of PDGFR antagonists in the treatment of cancer, alone and in combination with chemotherapy or other targeted agents. Extensive experimental data highlight the potential therapeutic advantage of targeting PDGFR. However, recent clinical data suggest that antagonism of this growth factor is associated with fluid accumulation that could obscure any clinical benefit. Further clinical research is required to optimise inhibition of this cytokine-receptor system.
dc.language.isoenen
dc.subjectCanceren
dc.subjectOvarian Canceren
dc.subjectProstatic Canceren
dc.subject.meshAngiogenesis Inhibitors
dc.subject.meshAnimals
dc.subject.meshDermatofibrosarcoma
dc.subject.meshFemale
dc.subject.meshGlioma
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshNeoplasms
dc.subject.meshNeovascularization, Pathologic
dc.subject.meshOvarian Neoplasms
dc.subject.meshProstatic Neoplasms
dc.subject.meshReceptors, Platelet-Derived Growth Factor
dc.titlePlatelet-derived growth factor receptor (PDGFR): a target for anticancer therapeutics.en
dc.typeArticleen
dc.contributor.departmentCancer Research UK Department Medical Oncology, Christie Hospital, Manchester M20 4BX, UK. Ruth.Board@christie-tr.nwest.nhs.uken
dc.identifier.journalDrug Resistance Updatesen
html.description.abstractPlatelet-derived growth factors (PDGFs) and their tyrosine kinase receptors (PDGFRs) have been implicated in the pathogenesis of a number of tumor types and play an important role in angiogenesis. Tumor growth can be promoted by PDGF via autocrine stimulation of malignant cells, by overexpression or overactivation of PDGFRs, or by stimulation of angiogenesis within the tumor. These mechanisms could provide possible therapeutic targets. PDGFR blockade may also lower the interstitial fluid pressure within solid tumors and enhance drug delivery. Here we discuss the possible therapeutic roles of PDGFR antagonists in the treatment of cancer, alone and in combination with chemotherapy or other targeted agents. Extensive experimental data highlight the potential therapeutic advantage of targeting PDGFR. However, recent clinical data suggest that antagonism of this growth factor is associated with fluid accumulation that could obscure any clinical benefit. Further clinical research is required to optimise inhibition of this cytokine-receptor system.


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