TY - JOUR
T1 - Involvement of EphA2 in head and neck squamous cell carcinoma
T2 - mRNA expression, loss of heterozygosity and immunohistochemical studies
AU - Rivera, Rosario S.
AU - Gunduz, Mehmet
AU - Nagatsuka, Hitoshi
AU - Gunduz, Esra
AU - Cengiz, Beyhan
AU - Fukushima, Kunihiro
AU - Beder, Levent Bekir
AU - Pehlivan, Davut
AU - Yamanaka, Noboru
AU - Shimizu, Kenji
AU - Nagai, Noriyuki
PY - 2008/5
Y1 - 2008/5
N2 - EphA2 is a 130-kDa transmembrane protein primarily found in adult human epithelial cells and is a member of one of the largest receptor tyrosine kinases. It is located on 1p36.1, a genetic hot spot in cancer. EphA2 over-expression has been observed in aggressive solid tumors and its potential role in tumorigenesis, which includes cell growth, survival, migration and angiogenesis have been reported. However, the role of EphA2 remains unknown in head and neck cancer. In this study, we investigated the genetic profile of EphA2 in primary head and neck squamous cell carcinoma (HNSCC) by determining mRNA level, status of loss of heterozygosity and protein expression. mRNA expression was also correlated with clinicopathological data. Infrequent loss of heterozygosity (20%) was observed, though a 10-fold increase of mRNA expression in tumors compared to normal tissues was noted. A significant number of samples with normal to high mRNA expression was observed among patients with regional metastasis, with T3-T4 tumor size and with moderate to poor differentiation. However, statistical studies did not show any correlation between mRNA expression and any of the clinicopathological parameters. Tumor cells expressed EphA2 protein, but only weakly. These results suggest thate EphA2 might be involved in the early development of HNSCC although not directly responsible for its progression.
AB - EphA2 is a 130-kDa transmembrane protein primarily found in adult human epithelial cells and is a member of one of the largest receptor tyrosine kinases. It is located on 1p36.1, a genetic hot spot in cancer. EphA2 over-expression has been observed in aggressive solid tumors and its potential role in tumorigenesis, which includes cell growth, survival, migration and angiogenesis have been reported. However, the role of EphA2 remains unknown in head and neck cancer. In this study, we investigated the genetic profile of EphA2 in primary head and neck squamous cell carcinoma (HNSCC) by determining mRNA level, status of loss of heterozygosity and protein expression. mRNA expression was also correlated with clinicopathological data. Infrequent loss of heterozygosity (20%) was observed, though a 10-fold increase of mRNA expression in tumors compared to normal tissues was noted. A significant number of samples with normal to high mRNA expression was observed among patients with regional metastasis, with T3-T4 tumor size and with moderate to poor differentiation. However, statistical studies did not show any correlation between mRNA expression and any of the clinicopathological parameters. Tumor cells expressed EphA2 protein, but only weakly. These results suggest thate EphA2 might be involved in the early development of HNSCC although not directly responsible for its progression.
KW - EphA2
KW - Head and neck squamous cell carcinoma
KW - Immunohistochemistry
KW - Loss of heterozygosity
KW - mRNA expression
UR - http://www.scopus.com/inward/record.url?scp=47549099026&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=47549099026&partnerID=8YFLogxK
U2 - 10.3892/or.19.5.1079
DO - 10.3892/or.19.5.1079
M3 - Article
C2 - 18425361
AN - SCOPUS:47549099026
SN - 1021-335X
VL - 19
SP - 1079
EP - 1084
JO - Oncology Reports
JF - Oncology Reports
IS - 5
ER -