Expression and loss of heterozygosity of c‐met proto‐oncogene in primary breast cancer
pmid: 7564388
Expression and loss of heterozygosity of c‐met proto‐oncogene in primary breast cancer
AbstractThe c‐met proto‐oncogene encodes the receptor to hepatocyte growth factor‐scatter factor (HGF‐SF), a mesenchyme‐derived cytokine with cell‐dissociating, invasion, and angiogenic properties. The expression of c‐met in breast cancer is the subject of controversy; 111 primary breast cancers were examined for LOH of c‐met by Southern blot electrophoresis. c‐met expression was measured in a further 40 patients with breast cancer and in 8 patients with benign breast disease by flow cytometry. LOH of c‐met was detected in only 4% of informative breast cancers. Expression of c‐met was significantly greater in patients with breast cancer than in those with benign breast disease (P <0.01, Mann‐Whitney). There was no correlation however between increased c‐met expression and clinicopatho‐logical prognostic variables. These results do not support the role of c‐met as a tumour suppressor gene in breast cancer but suggest increased receptor expression in malignant breast disease. The significance of this increased expression in breast cancer is the subject of further investigation. © 1995 Wiley‐Liss, Inc.
- University of Glasgow United Kingdom
- Kings College London, University of London United Kingdom
- NHS Greater Glasgow and Clyde United Kingdom
- Western Infirmary United Kingdom
- King's College London United Kingdom
Heterozygote, Blotting, Hepatocyte Growth Factor, 610, Receptor Protein-Tyrosine Kinases, Breast Neoplasms, Proto-Oncogene Proteins c-met, Flow Cytometry, Prognosis, Proto-Oncogene Mas, Blotting, Southern, Breast Diseases, Humans, Female, Southern
Heterozygote, Blotting, Hepatocyte Growth Factor, 610, Receptor Protein-Tyrosine Kinases, Breast Neoplasms, Proto-Oncogene Proteins c-met, Flow Cytometry, Prognosis, Proto-Oncogene Mas, Blotting, Southern, Breast Diseases, Humans, Female, Southern
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