Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11844
Title: Targeting the ERBB family in cancer: couples therapy.
Authors: Tebbutt, Niall C;Pedersen, Mikkel W;Johns, Terrance G
Affiliation: Ludwig Oncology Unit, Austin Health, Studley Road, Heidelberg, Victoria 3084, Australia
Issue Date: 16-Aug-2013
Citation: Nature Reviews. Cancer 2013; 13(9): 663-73
Abstract: The ERBB family of receptor tyrosine kinases has a central role in the tumorigenesis of many types of solid tumour. Various therapeutics targeting these receptors have been approved for the treatment of several cancers. Considerable preclinical data have shown that the administration of two inhibitors against an individual ERBB family member--particularly epidermal growth factor receptor (EGFR) or ERBB2--leads to markedly higher antitumour activity than the administration of single agents. This Opinion article describes the preclinical and clinical performance of these dual-targeting approaches, discusses the key mechanisms that mediate their increased efficacy and highlights areas for ongoing investigation.
Internal ID Number: 23949426
URI: http://ahro.austin.org.au/austinjspui/handle/1/11844
DOI: 10.1038/nrc3559
URL: http://www.ncbi.nlm.nih.gov/pubmed/23949426
Type: Journal Article
Subjects: Antibodies, Monoclonal.administration & dosage.pharmacology
Antineoplastic Combined Chemotherapy Protocols.therapeutic use
Drug Resistance, Neoplasm
Humans
Neoplasms.drug therapy.enzymology
Protein Kinase Inhibitors.administration & dosage.pharmacology
Receptor, Epidermal Growth Factor.antagonists & inhibitors.immunology.metabolism
Receptor, ErbB-2.antagonists & inhibitors.immunology.metabolism
Appears in Collections:Journal articles

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