Source:http://linkedlifedata.com/resource/pubmed/id/12845624
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-7-7
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pubmed:abstractText |
EGFr/HER1 and c-erbB-2/HER2 expression are associated with poor prognosis in breast cancer. The type I receptor tyrosine kinase (RTK) family to which they belong has four members (HER1-4). In this study, expression of HER1-4 and oestrogen receptor (ER) expression were determined by immunohistochemistry in 220 breast carcinomas. Elevated expression of HER1 was observed in 16.4%, HER2 in 22.8%, HER3 in 17.5%, and HER4 in 11.9% of these tumours. Patients whose tumours overexpressed HER1, 2 or 3 had reduced survival (p= <0.001), whereas those whose tumours overexpressed HER4 had increased survival (p=0.013); 38.6% of cases overexpressed one or more of HER1, 2 or 3. HER4 was rarely overexpressed with other HERs (1.4% of cases). Cox's multiple regression analysis demonstrated that overexpression of HER1/2/3, HER4, and standard prognostic indicators independently affected survival. HER1-3 expression was related to ER negativity (p<0.0001, chi2). Patients with ER-positive, HER1-3-positive tumours had a significantly poorer survival (p<0.001) than those with ER-positive/HER-negative or HER4-positive tumours. Expression of HER RTKs displays complex interactions between different family members. There is a strong interaction, in terms of survival, between HER expression and ER expression. The development of HER-targeted agents (eg Herceptin, Iressa), and agents targeted at the downstream signalling pathways, therefore provides new possibilities in the treatment of breast cancer.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, erbB-2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, erbB-3,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen,
http://linkedlifedata.com/resource/pubmed/chemical/receptor tyrosine-protein kinase...
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0022-3417
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2003 John Wiley & Sons, Ltd.
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pubmed:issnType |
Print
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pubmed:volume |
200
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
290-7
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pubmed:dateRevised |
2011-11-2
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pubmed:meshHeading |
pubmed-meshheading:12845624-Breast Neoplasms,
pubmed-meshheading:12845624-Female,
pubmed-meshheading:12845624-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:12845624-Genes, erbB,
pubmed-meshheading:12845624-Genes, erbB-1,
pubmed-meshheading:12845624-Genes, erbB-2,
pubmed-meshheading:12845624-Humans,
pubmed-meshheading:12845624-Immunohistochemistry,
pubmed-meshheading:12845624-Prognosis,
pubmed-meshheading:12845624-Protein-Tyrosine Kinases,
pubmed-meshheading:12845624-Receptor, Epidermal Growth Factor,
pubmed-meshheading:12845624-Receptor, erbB-2,
pubmed-meshheading:12845624-Receptor, erbB-3,
pubmed-meshheading:12845624-Receptors, Estrogen
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pubmed:year |
2003
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pubmed:articleTitle |
Expression of the HER1-4 family of receptor tyrosine kinases in breast cancer.
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pubmed:affiliation |
University Department of Surgery, Glasgow Royal Infirmary, Glasgow G31 2ER, UK.
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pubmed:publicationType |
Journal Article
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