Publication: EGFR expression and activation are common in HER2 positive and triple-negative breast tumours
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Date
2010
Authors
Koletsa, T. ; Kotoula, Vassiliki ; Karayannopoulou, Georgia ; Nenopoulou, E.
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Publisher
Murcia : F. Hernández
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DOI
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info:eu-repo/semantics/article
Description
Abstract
EGFR has been associated with unfavourable
prognosis in patients with triple-negative breast
carcinomas, although little is known about EGFR
activation in these tumours. In a series of breast
carcinomas (archived formalin fixed tumours, n=100),
we investigated EGFR phosphorylation status at Tyr992
(pEGFR-Y992) and Tyr1068 (pEGFR-Y1068) by
immunohistochemistry, along with EGFR protein
expression (extracellular domain), gene amplification
status (fluorescent in situ hybridization) and
conventional clinicopathologic parameters. EGFR
protein was present in 21.9%, while phosphorylation at
Y1068 and Y992 was observed in 27.8% and 50.5% of
tumours, respectively. None of the tumours showed
EGFR gene amplification, whereas 21.1% exhibited
chromosome 7 polysomy. The above EGFR parameters
were usually not simultaneously detected and were not
associated with each other. High grade (p=0.003), lymph
node positive (p=0.045), estrogen receptor (ER) negative
(p<0.001) tumours often expressed EGFR protein.
EGFR-Y992 and Y1068 phosphorylation was inversely
associated with ER presence (p=0.023 and p=0.029,
respectively) but positively with HER2 expression status
(p<0.001 and p=0.002, respectively). The global
positivity for any EGFR parameter did not significantly
differ between triple-negative and HER2 positive
tumours. In conclusion, EGFR phosphorylation is
commonly encountered in breast carcinomas, although
unrelated to EGFR protein presence and gene
amplification. EGFR may appear activated even in cases
where the extracellular domain of this protein is not
observed with immunohistochemistry. These findings
may be useful for further studies aiming at the assessment of EGFR parameters on this type of material
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