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Article: Up-regulation of the protein tyrosine phosphatase SHP-1 in human breast cancer and correlation with GRB2 expression

TitleUp-regulation of the protein tyrosine phosphatase SHP-1 in human breast cancer and correlation with GRB2 expression
Authors
Issue Date2000
Citation
International Journal of Cancer, 2000, v. 88, n. 3, p. 363-368 How to Cite?
AbstractThe protein tyrosine phosphatase SHP-1 is predominantly expressed in hemopoietic cell lineages, where its function is relatively well defined. However, its expression profile also extends to certain epithelial cell types. Furthermore, the negative regulatory role of this enzyme in hemopoietlc cell signaling may not apply to other systems, where positive effects on particular tyrosine kinase signaling pathways have been described. Expression of SHP-1 was therefore investigated in human breast cancer cell lines and primary breast cancers. Differential expression of SHP-1 mRNA was observed among the 19 breast cancer cell lines examined, and in an analysis of 72 primary breast cancers, SHP-1 mRNA expression was increased 2- to 12-fold relative to normal breast epithelial cells in 58% of the samples. Interestingly, a subset of the cancers also over-expressed GRB2 mRNA by 2- to 7-fold, and a significant (p < 0.01) positive correlation was observed between SHP-1 and GRB2 mRNA expression. Since these proteins can bind to each other and regulate MEK/MAP kinase activation, their co-ordinate up-regulation may amplify tyrosine kinase signaling in breast cancer cells. (C) 2000 Wiley-Liss, Inc.
Persistent Identifierhttp://hdl.handle.net/10722/326444
ISSN
2023 Impact Factor: 5.7
2023 SCImago Journal Rankings: 2.131
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYip, Sonia S.-
dc.contributor.authorCrew, A. Jayne-
dc.contributor.authorGee, Julia M.W.-
dc.contributor.authorHui, Rina-
dc.contributor.authorBlamey, Roger W.-
dc.contributor.authorRobertson, John F.R.-
dc.contributor.authorNicholson, Robert I.-
dc.contributor.authorSutherland, Robert L.-
dc.contributor.authorDaly, Roger J.-
dc.date.accessioned2023-03-10T02:19:19Z-
dc.date.available2023-03-10T02:19:19Z-
dc.date.issued2000-
dc.identifier.citationInternational Journal of Cancer, 2000, v. 88, n. 3, p. 363-368-
dc.identifier.issn0020-7136-
dc.identifier.urihttp://hdl.handle.net/10722/326444-
dc.description.abstractThe protein tyrosine phosphatase SHP-1 is predominantly expressed in hemopoietic cell lineages, where its function is relatively well defined. However, its expression profile also extends to certain epithelial cell types. Furthermore, the negative regulatory role of this enzyme in hemopoietlc cell signaling may not apply to other systems, where positive effects on particular tyrosine kinase signaling pathways have been described. Expression of SHP-1 was therefore investigated in human breast cancer cell lines and primary breast cancers. Differential expression of SHP-1 mRNA was observed among the 19 breast cancer cell lines examined, and in an analysis of 72 primary breast cancers, SHP-1 mRNA expression was increased 2- to 12-fold relative to normal breast epithelial cells in 58% of the samples. Interestingly, a subset of the cancers also over-expressed GRB2 mRNA by 2- to 7-fold, and a significant (p < 0.01) positive correlation was observed between SHP-1 and GRB2 mRNA expression. Since these proteins can bind to each other and regulate MEK/MAP kinase activation, their co-ordinate up-regulation may amplify tyrosine kinase signaling in breast cancer cells. (C) 2000 Wiley-Liss, Inc.-
dc.languageeng-
dc.relation.ispartofInternational Journal of Cancer-
dc.titleUp-regulation of the protein tyrosine phosphatase SHP-1 in human breast cancer and correlation with GRB2 expression-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/1097-0215(20001101)88:3<363::AID-IJC7>3.0.CO;2-4-
dc.identifier.pmid11054664-
dc.identifier.scopuseid_2-s2.0-0033809911-
dc.identifier.volume88-
dc.identifier.issue3-
dc.identifier.spage363-
dc.identifier.epage368-
dc.identifier.isiWOS:000089710600007-

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