TY - JOUR
T1 - Aberrant expression of the human epidermal growth factor receptor 2 oncogene is not a common feature in osteosarcoma
AU - Baumhoer, Daniel
AU - Smida, Jan
AU - Specht, Katja
AU - Bink, Karin
AU - Quintanilla-Martinez, Leticia
AU - Rosemann, Michael
AU - Siggelkow, Heide
AU - Nathrath, Walter B.J.
AU - Atkinson, Michael J.
AU - Bielack, Stefan
AU - Jundt, Gernot
AU - Nathrath, Michaela
N1 - Funding Information:
Grant support: Daniel Baumhoer was supported by the Novartis Foundation , formerly Ciba-Geigy-Jubilee-Foundation, Basel, Switzerland. Jan Smida and Michaela Nathrath are members of the Translational Sarcoma Research Network supported by the Federal Ministry of Education and Research (BMBF), Bonn, Germany. Michaela Nathrath is supported by the Wilhelm Sander-Stiftung, Munich, Germany and the Elterninitiative krebskranke Kinder München eV, Munich, Germany .
PY - 2011/6
Y1 - 2011/6
N2 - Human epidermal growth factor receptor 2 expression in osteosarcoma and its relationship to prognosis have been the subject of several conflicting reports, most of them relying on immunohistochemical studies. Because the urgent need of prognostic markers and effective new treatment options for osteosarcoma patients, we evaluated the role of human epidermal growth factor receptor 2 in 2 well-characterized sets of pretherapeutic osteosarcoma samples (46 paraffin-embedded and 46 fresh-frozen biopsy samples) using immunohistochemistry with 2 different antibodies [DAKO A0485 (Glostrup, Denmark) and Novocastra CB11 (Newcastle, UK)] as well as fluorescence in situ hybridization, real-time polymerase chain reaction, and SNP array analyses and correlated our findings with clinicopathological parameters. However, our study failed to detect unequivocal evidence of human epidermal growth factor receptor 2 gene amplification or overexpression of human epidermal growth factor receptor 2 messenger RNA or protein in any of the investigated tumors. Only in a small subset of samples, a moderate increase in messenger RNA levels (13.6%) or focal membranous immunoreactivity (8.7%; A0485) was detected but did not correlate with survival or response to chemotherapy. Cytoplasmic staining was identified more frequently (63%; CB11) but again did not show any association with clinicopathological parameters. In conclusion, our study does not support a role for human epidermal growth factor receptor 2 as a prognostic marker in osteosarcoma.
AB - Human epidermal growth factor receptor 2 expression in osteosarcoma and its relationship to prognosis have been the subject of several conflicting reports, most of them relying on immunohistochemical studies. Because the urgent need of prognostic markers and effective new treatment options for osteosarcoma patients, we evaluated the role of human epidermal growth factor receptor 2 in 2 well-characterized sets of pretherapeutic osteosarcoma samples (46 paraffin-embedded and 46 fresh-frozen biopsy samples) using immunohistochemistry with 2 different antibodies [DAKO A0485 (Glostrup, Denmark) and Novocastra CB11 (Newcastle, UK)] as well as fluorescence in situ hybridization, real-time polymerase chain reaction, and SNP array analyses and correlated our findings with clinicopathological parameters. However, our study failed to detect unequivocal evidence of human epidermal growth factor receptor 2 gene amplification or overexpression of human epidermal growth factor receptor 2 messenger RNA or protein in any of the investigated tumors. Only in a small subset of samples, a moderate increase in messenger RNA levels (13.6%) or focal membranous immunoreactivity (8.7%; A0485) was detected but did not correlate with survival or response to chemotherapy. Cytoplasmic staining was identified more frequently (63%; CB11) but again did not show any association with clinicopathological parameters. In conclusion, our study does not support a role for human epidermal growth factor receptor 2 as a prognostic marker in osteosarcoma.
KW - ERBB2
KW - FISH
KW - HER-2/neu
KW - Immunohistochemistry
KW - Osteosarcoma
KW - Single nucleotide polymorphism (SNP) array
KW - qRT-PCR
UR - http://www.scopus.com/inward/record.url?scp=79956125778&partnerID=8YFLogxK
U2 - 10.1016/j.humpath.2010.09.016
DO - 10.1016/j.humpath.2010.09.016
M3 - Article
AN - SCOPUS:79956125778
SN - 0046-8177
VL - 42
SP - 859
EP - 866
JO - Human Pathology
JF - Human Pathology
IS - 6
ER -