ETS-1 proto-oncogene as a key newcomer molecule to predict invasiveness in laryngeal carcinoma

被引:11
作者
Calli, Aylin Orgen [1 ]
Sari, Aysegul [1 ]
Cakalagaoglu, Fulya [1 ]
Altinboga, Aysegul Aksoy [1 ]
Oncel, Semih [2 ]
机构
[1] Izmir Training & Res Hosp, Dept Pathol, Izmir, Turkey
[2] Izmir Training & Res Hosp, Dept Head & Neck Surg, Izmir, Turkey
关键词
ETS-1; oncoprotein; Immunohistochemistry; Larynx; Squamous carcinoma; Invasiveness; SQUAMOUS-CELL CARCINOMA; TRANSCRIPTION FACTOR; PLASMINOGEN-ACTIVATOR; BREAST-CANCER; GASTRIC-CARCINOMA; ASTROCYTIC TUMORS; POOR-PROGNOSIS; EXPRESSION; MARKER; OVEREXPRESSION;
D O I
10.1016/j.prp.2011.07.010
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
ETS-1 protein is one of the key regulators in tumor invasion and progression. We aimed to evaluate the role of ETS-1 in the invasiveness and progression of laryngeal squamous carcinoma, as well as to determine the correlations between clinicopathological characteristics and expression of this molecule. We assessed the levels of ETS-1 in a total of 96 laryngeal specimens of varying degrees of dysplasia, microinvasive squamous carcinoma (8), and invasive squamous carcinoma (60), using normal mucosal epithelium (10) as a positive control. The relationship between ETS-1 expression and clinicopathological parameters of laryngeal carcinoma was also analyzed. We found a significantly higher ETS-1 expression in invasive laryngeal squamous cell carcinomas than in dysplasia (P < 0.001). A correlation between ETS-1 expression scores and grade was detected - T factor, stage, cartilage invasion, lymph node metastasis, as well as depth of invasion in laryngeal tumors. Our study is the first to demonstrate that ETS-1 expression is significantly increased in invasive carcinoma, but it is absent in low-moderate grade laryngeal dysplasia and non-neoplastic laryngeal mucosa. This data suggest that ETS-1 expression may play an important role in tumor invasion, and may function in the initiation of the invasive process in laryngeal squamous cell carcinoma. (C) 2011 Elsevier GmbH. All rights reserved.
引用
收藏
页码:628 / 633
页数:6
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