Hao X, Palazzo J P, Ilyas M, Tomlinson I, Talbot I C
Academic Department of Pathology, St Mark's Hospital, Harrow, U.K.
Anticancer Res. 1997 May-Jun;17(3C):2241-7.
E-cadherin is crucial to the intercellular adherens junctions which are involved in the organisation and maintenance of epithelial structure and suppression of tumour invasion. E-cadherin is associated with the actin cytoskeleton via cytoplasmic proteins, including alpha-, beta- and gamma-catenins, which together form the cadherin/catenin complex. To evaluate changes of the molecules of the cadherin/catenin complex in colorectal carcinogenesis, seventy-four sporadic adenomas, samples of histologically normal epithelium adjacent to 65 adenomas, and 52 carcinomas arising in adenomas were investigated by immunohistochemistry. All normal epithelial cells showed a uniform membranous staining pattern for E-cadherin, alpha-, beta-, and gamma-catenin. Decreased expression of all 4 proteins occurred in parallel in adenomas and carcinomas (in all cases, p < 10(-5). Decreased expression of the cadherin/catenin complex in adenomas was associated with increasing severity of dysplasia (p < 0.001, for E-cadherin, alpha-, and gamma-catenin, p < 0.005 for beta-catenin). Carcinomas displayed significantly reduced expression of the cadherin/catenin complex compared with their associated adenomas (all p < 0.001). The results directly confirm that colorectal tumour progression and invasion is associated with disruption of the cadherin/catenin complex and suggest that the genetic changes and transcriptional modulation of catenins underlying this progression may affect all members of the complex.
E-钙黏蛋白对于细胞间黏附连接至关重要,该连接参与上皮结构的组织和维持以及肿瘤侵袭的抑制。E-钙黏蛋白通过包括α-、β-和γ-连环蛋白在内的细胞质蛋白与肌动蛋白细胞骨架相关联,这些蛋白共同形成钙黏蛋白/连环蛋白复合物。为了评估钙黏蛋白/连环蛋白复合物分子在结直肠癌发生过程中的变化,采用免疫组织化学方法对74个散发性腺瘤、65个腺瘤旁组织学正常上皮样本以及52个腺瘤中发生的癌进行了研究。所有正常上皮细胞对E-钙黏蛋白、α-、β-和γ-连环蛋白均呈现均匀的膜染色模式。在腺瘤和癌中,所有这4种蛋白的表达均平行下降(在所有病例中,p < 10⁻⁵)。腺瘤中钙黏蛋白/连环蛋白复合物表达的下降与发育异常的严重程度增加相关(对于E-钙黏蛋白、α-和γ-连环蛋白,p < 0.001;对于β-连环蛋白,p < 0.005)。与相关腺瘤相比,癌中钙黏蛋白/连环蛋白复合物的表达显著降低(所有p < 0.001)。结果直接证实结直肠肿瘤的进展和侵袭与钙黏蛋白/连环蛋白复合物的破坏有关,并表明这种进展背后连环蛋白的基因变化和转录调节可能影响该复合物的所有成员。