Smythe W R, Williams J P, Wheelock M J, Johnson K R, Kaiser L R, Albelda S M
M.D. Anderson Cancer Center, Department of Thoracic and Cardiovascular Surgery, The University of Texas, Houston 77030, USA. rsmythenotes.mdacc.tmc.edu.
Lung Cancer. 1999 Jun;24(3):157-68. doi: 10.1016/s0169-5002(99)00032-x.
Cadherins are transmembrane cell adhesion molecules (CAMS) that mediate cell-cell interactions and are important for maintenance of epithelial cell integrity. This function is dependent on an indirect interaction between the cytoplasmic domain of the cadherin molecule with three cytoplasmic proteins known as alpha-, beta-, and gamma-catenin (-cat). Growing evidence suggests that alterations in cadherin or catenin expression or function may be important to the development of an invasive or metastatic phenotype. Immunohistochemical techniques were used to study the expression of the two major epithelial cadherins, E-cadherin (E-cad) and P-cadherin (P-cad) as well as alpha- and gamma-cat in normal bronchial epithelium and in a series of carefully TMN-staged pulmonary adenocarcinomas (n = 21) and squamous cell carcinomas (n = 7). The cadherin profile of normal pseudostratified bronchial epithelium was heterogeneous. Basilar cells strongly expressed P-cad, alpha- and gamma-cat, while columnar cells moderately expressed E-cad, alpha- and gamma-cat. In contrast to other epithelial tumors, E-cad on non-small cell lung carcinomas was actually upregulated, however, a decrease in P-cad expression was noted in 68%. At least one cadherin or catenin was downregulated, compared to normal bronchial epithelium, in 82% of tumors examined. With the exception of an association between loss of P-cad expression and poorly differentiated state, changes in cadherin and catenin expression levels were not significantly correlated to tumor stage, cell type, or nodal status. These findings illustrate that alteration of expression of cadherins and catenins are often found in non-small cell lung carcinoma when compared to the progenitor bronchial epithelium, and may play a role in the development of the malignant phenotype.
钙黏着蛋白是跨膜细胞黏附分子(CAMS),介导细胞间相互作用,对维持上皮细胞完整性很重要。该功能依赖于钙黏着蛋白分子胞质结构域与三种胞质蛋白(称为α -、β - 和γ - 连环蛋白(-cat))之间的间接相互作用。越来越多的证据表明,钙黏着蛋白或连环蛋白表达或功能的改变可能对侵袭性或转移表型的发展很重要。免疫组织化学技术用于研究两种主要上皮钙黏着蛋白E - 钙黏着蛋白(E - cad)和P - 钙黏着蛋白(P - cad)以及α - 和γ - cat在正常支气管上皮以及一系列经过仔细TMN分期的肺腺癌(n = 21)和鳞状细胞癌(n = 7)中的表达。正常假复层支气管上皮的钙黏着蛋白谱是异质性的。基底细胞强烈表达P - cad、α - 和γ - cat,而柱状细胞中度表达E - cad、α - 和γ - cat。与其他上皮肿瘤不同,非小细胞肺癌中的E - cad实际上是上调的,然而,68%的病例中观察到P - cad表达下降。与正常支气管上皮相比,在82%的检测肿瘤中至少有一种钙黏着蛋白或连环蛋白下调。除了P - cad表达缺失与低分化状态之间的关联外,钙黏着蛋白和连环蛋白表达水平的变化与肿瘤分期、细胞类型或淋巴结状态无显著相关性。这些发现表明,与祖代支气管上皮相比,非小细胞肺癌中经常发现钙黏着蛋白和连环蛋白表达的改变,并且可能在恶性表型的发展中起作用。