Yüce İmdat, Çağlı Sedat, Canöz Özlem, Güney Ercihan
Department of ENT, Kayseri Training and Research Hospital, Kayseri, Turkey.
Department of ENT, Erciyes University School of Medicine, Kayseri, Turkey.
Am J Otolaryngol. 2015 Nov-Dec;36(6):736-40. doi: 10.1016/j.amjoto.2015.08.006. Epub 2015 Aug 18.
To evaluate the value of E-cadherin and epithelial cell adhesion molecule (Ep-CAM) expression in laryngeal biopsy materials for predicting cervical lymph node metastasis in patients with supraglottic laryngeal carcinoma.
All patients participating in the study were selected from among the surgically treated patients at the department of Otolaryngology, Head and Neck Surgery, Erciyes University School of Medicine between 1991 and 2005. The study consisted of thirty patients who had pathologically metastatic lymph nodes (pN+ group) and 30 age-, sex-, T value- and differentiation matched patients without pathologically metastatic lymph nodes (pN0 group). Immunohistochemical studies were performed with E-cadherin and Ep-CAM antibodies on representative tumor sections collected from paraffin sections of laryngeal biopsy materials. The expression of E-cadherin and Ep-CAM was compared between the pN0 and pN+ groups. The association between immunostaining of E-cadherin and Ep-CAM was also evaluated.
There was no significant difference between the two groups in terms of E-cadherin and Ep-CAM expression. There was also a very poor agreement between the expression of E-cadherin and Ep-CAM.
Multi-institutional and multidisciplinary immunohistochemical studies conducted with standardized methodology and also with more patient participation may help to obtain more specific results.
评估声门上型喉癌患者喉活检材料中E-钙黏蛋白和上皮细胞黏附分子(Ep-CAM)表达对预测颈部淋巴结转移的价值。
参与本研究的所有患者均选自2005年间埃尔西耶斯大学医学院耳鼻咽喉头颈外科接受手术治疗的患者。该研究包括30例有病理证实的转移性淋巴结患者(pN+组)和30例年龄、性别、T值及分化程度与之匹配但无病理证实的转移性淋巴结患者(pN0组)。采用E-钙黏蛋白和Ep-CAM抗体对从喉活检材料石蜡切片中获取的代表性肿瘤切片进行免疫组织化学研究。比较pN0组和pN+组中E-钙黏蛋白和Ep-CAM的表达情况。同时评估E-钙黏蛋白和Ep-CAM免疫染色之间的相关性。
两组在E-钙黏蛋白和Ep-CAM表达方面无显著差异。E-钙黏蛋白和Ep-CAM的表达之间也存在非常低的一致性。
采用标准化方法并纳入更多患者进行多机构、多学科免疫组织化学研究可能有助于获得更具特异性的结果。