TY - JOUR
T1 - Tissue microarray-based study of patients with lymph node-positive breast cancer shows tyrosine phosphorylation of signal transducer and activator of transcription 3 (tyrosine705-STAT3) is a marker of good prognosis
AU - Sonnenblick, Amir
AU - Shriki, Anat
AU - Galun, Eithan
AU - Axelrod, Jonathan H.
AU - Daum, Hagit
AU - Rottenberg, Yakir
AU - Hamburger, Tamar
AU - Mali, Bela
AU - Peretz, Tamar
N1 - Funding Information:
Acknowledgements This work was supported by the Sharett Institute of Oncology and Goldyne Savad Institute of Gene Therapy, and partially by grants from Hadassah Medical Center and the American Physicians’ Fellowship (APF) for Medicine in Israel.
PY - 2012/3
Y1 - 2012/3
N2 - Background Although lymph node-positive breast cancers are associated with poorer prognosis, individual patients may have different clinical outcomes. Signal transducer and activator of transcription 3 (STAT3) is a point of convergence for numerous oncogenic signalling pathways. The goal of this study was to determine the prognostic value of phosphorylated (tyrosine705)-STAT3 in node-positive breast cancer patients. Methods Immunohistochemical analysis of Phospho- STAT3 was performed on a tissue microarray of breast cancer specimens. The expression pattern of Phospho-STAT3 was correlated with survival outcome, and clinical and pathological parameters. Results Out of 125 interpretable tumours, positive Phospho- STAT3 nuclear expression was seen in 35 (28%) of tumours. There was no significant relationship between Phospho-STAT3 expression and clinical-pathological parameters including age, hormonal receptor status, grade and tumour size. Interestingly positive tumours had a significantly improved disease-free survival at 5 years (p=0.035). Additionally, positive Phospho-STAT3 nuclear expression was correlated with significantly improved survival at both 5 years (p=0.023) and 10 years (p=0.026). Finally, in multivariate analyses Phospho-STAT3 was found to be an independent prognostic marker of overall survival in node-positive breast cancer patients. Conclusion These findings support the role of Phospho- STAT3 as an important independent prognostic marker in node-positive breast cancer patients.
AB - Background Although lymph node-positive breast cancers are associated with poorer prognosis, individual patients may have different clinical outcomes. Signal transducer and activator of transcription 3 (STAT3) is a point of convergence for numerous oncogenic signalling pathways. The goal of this study was to determine the prognostic value of phosphorylated (tyrosine705)-STAT3 in node-positive breast cancer patients. Methods Immunohistochemical analysis of Phospho- STAT3 was performed on a tissue microarray of breast cancer specimens. The expression pattern of Phospho-STAT3 was correlated with survival outcome, and clinical and pathological parameters. Results Out of 125 interpretable tumours, positive Phospho- STAT3 nuclear expression was seen in 35 (28%) of tumours. There was no significant relationship between Phospho-STAT3 expression and clinical-pathological parameters including age, hormonal receptor status, grade and tumour size. Interestingly positive tumours had a significantly improved disease-free survival at 5 years (p=0.035). Additionally, positive Phospho-STAT3 nuclear expression was correlated with significantly improved survival at both 5 years (p=0.023) and 10 years (p=0.026). Finally, in multivariate analyses Phospho-STAT3 was found to be an independent prognostic marker of overall survival in node-positive breast cancer patients. Conclusion These findings support the role of Phospho- STAT3 as an important independent prognostic marker in node-positive breast cancer patients.
KW - Breast cancer
KW - Immunohistochemistry
KW - Phosphorylation
KW - STAT3
KW - Tissue microarray
UR - http://www.scopus.com/inward/record.url?scp=84860760469&partnerID=8YFLogxK
U2 - 10.1007/s12094-012-0789-z
DO - 10.1007/s12094-012-0789-z
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 22374428
AN - SCOPUS:84860760469
SN - 1699-048X
VL - 14
SP - 232
EP - 236
JO - Clinical and Translational Oncology
JF - Clinical and Translational Oncology
IS - 3
ER -