TY - JOUR
T1 - Expression of constitutively activated EGFRvIII in non-small cell lung cancer
AU - Okamoto, Isamu
AU - Kenyon, Lawrence C.
AU - Emlet, David R.
AU - Mori, Takeshi
AU - Sasaki, Ji Ichiro
AU - Hirosako, Susumu
AU - Ichikawa, Yasuko
AU - Kishi, Hiroto
AU - Godwin, Andrew K.
AU - Yoshioka, Masakazu
AU - Suga, Moritaka
AU - Matsumoto, Mitsuhiro
AU - Wong, Albert J.
PY - 2003/1/1
Y1 - 2003/1/1
N2 - The epidermal growth factor receptor (EGFR) variant type III (variously called EGFRvIII, de2-7 EGFR or ΔEGFR) has an in-frame deletion of the extracellular domain and is found in numerous types of human tumors. Since EGFRvIII has been reported to be tumor-specific and has oncogenic potential, it is being investigated as a potential therapeutic target. Because the cell-specific expression of EGFRvIII in lung has not been well documented, we examined the expression of EGFRvIII in 76 non-small cell lung cancers (NSCLCs) and 10 non-neoplastic lung tissues by immunohistochemistry using a new monoclonal antibody specific for this variant receptor. We found a higher incidence (30 of 76, 39%) of enhanced EGFRvIII expression in NSCLC than previously described. Interestingly, the presence of EGFRvIII was also observed in several normal tissue components of lung (e.g., normal bronchial epithelium). Given the high prevalence of EGFRvIII in NSCLC, a newly developed phospho-specific (activated) EGFR antibody was employed for immunohistochemical analysis that permitted visualization of activated EGFR and/or EGFRvIII in tumors. This study presents evidence, for the first time, that EGFRvIII expressed in human tumors is phosphorylated and hence activated. Our results suggest that the sustained activation of EGFRvIII is implicated in the pathogenesis of NSCLC and thus EGFRvIII is a potential therapeutic target in this challenging disease.
AB - The epidermal growth factor receptor (EGFR) variant type III (variously called EGFRvIII, de2-7 EGFR or ΔEGFR) has an in-frame deletion of the extracellular domain and is found in numerous types of human tumors. Since EGFRvIII has been reported to be tumor-specific and has oncogenic potential, it is being investigated as a potential therapeutic target. Because the cell-specific expression of EGFRvIII in lung has not been well documented, we examined the expression of EGFRvIII in 76 non-small cell lung cancers (NSCLCs) and 10 non-neoplastic lung tissues by immunohistochemistry using a new monoclonal antibody specific for this variant receptor. We found a higher incidence (30 of 76, 39%) of enhanced EGFRvIII expression in NSCLC than previously described. Interestingly, the presence of EGFRvIII was also observed in several normal tissue components of lung (e.g., normal bronchial epithelium). Given the high prevalence of EGFRvIII in NSCLC, a newly developed phospho-specific (activated) EGFR antibody was employed for immunohistochemical analysis that permitted visualization of activated EGFR and/or EGFRvIII in tumors. This study presents evidence, for the first time, that EGFRvIII expressed in human tumors is phosphorylated and hence activated. Our results suggest that the sustained activation of EGFRvIII is implicated in the pathogenesis of NSCLC and thus EGFRvIII is a potential therapeutic target in this challenging disease.
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U2 - 10.1111/j.1349-7006.2003.tb01351.x
DO - 10.1111/j.1349-7006.2003.tb01351.x
M3 - Article
C2 - 12708474
AN - SCOPUS:0038324367
SN - 1347-9032
VL - 94
SP - 50
EP - 56
JO - Cancer Science
JF - Cancer Science
IS - 1
ER -