Interferon-inducible guanylate binding protein (GBP2) is associated with better prognosis in breast cancer and indicates an efficient T cell response

Background Recently, interferon-inducible guanylate binding protein (GBP2) has been discussed as a possible control factor in tumor development, which is controlled by p53, and inhibits NF-Kappa B and Rac protein as well as expression of matrix metalloproteinase 9. However, the potential role that G...

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Veröffentlicht in:Breast cancer (Tokyo, Japan) Japan), 2014-07, Vol.21 (4), p.491-499
Hauptverfasser: Godoy, Patricio, Cadenas, Cristina, Hellwig, Birte, Marchan, Rosemarie, Stewart, Joanna, Reif, Raymond, Lohr, Miriam, Gehrmann, Matthias, Rahnenführer, Jörg, Schmidt, Markus, Hengstler, Jan G.
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Sprache:eng
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Zusammenfassung:Background Recently, interferon-inducible guanylate binding protein (GBP2) has been discussed as a possible control factor in tumor development, which is controlled by p53, and inhibits NF-Kappa B and Rac protein as well as expression of matrix metalloproteinase 9. However, the potential role that GBP2 plays in tumor development and prognosis has not yet been studied. Methods We analyzed whether GBP2 mRNA levels are associated with metastasis-free interval in 766 patients with node negative breast carcinomas who did not receive systemic chemotherapy. Furthermore, response to anthracycline-based chemotherapy was studied in 768 breast cancer patients. Results High expression of GBP2 in breast carcinomas was associated with better prognosis in the univariate ( P  
ISSN:1340-6868
1880-4233
DOI:10.1007/s12282-012-0404-8