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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Journal of Surgical ...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Journal of Surgical Oncology
Article . 1995 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
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Expression and loss of heterozygosity of c‐met proto‐oncogene in primary breast cancer

Authors: Nagy, J; Clark, J S; Cooke, A; Campbell, A M; Connor, J M; Purushotham, A D; George, W D;

Expression and loss of heterozygosity of c‐met proto‐oncogene in primary breast cancer

Abstract

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.

Keywords

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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    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
15
Average
Top 10%
Top 10%