Department of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences of China Medical University, Shenyang, China.
J Pathol. 2010 Sep;222(1):76-88. doi: 10.1002/path.2742.
As a member of the catenin family, little is known about the clinical significance and possible mechanism of delta-catenin expression in numerous tumours. We examined the expression of delta-catenin by immunohistochemistry in 115 cases of non-small cell lung cancer (NSCLC) (including 65 cases with follow-up records and 50 cases with paired lymph node metastasis lesions). The mRNA and protein expression of delta-catenin was also detected in 30 cases of paired lung cancer tissues and normal lung tissues by RT-PCR and western blotting, respectively. Co-immunoprecipitation was used to examine whether delta-catenin competitively bound to E-cadherin with p120ctn in lung cancer cells or not. The effects of delta-catenin on the activity of small GTPases and the biological behaviour of lung cancer cells were explored by pull-down assay, flow cytometry, MTT, and Matrigel invasive assay. The results showed that the mRNA and protein expression of delta-catenin was increased in lung cancer tissues; the positive expression rate of delta-catenin was significantly increased in adenocarcinoma, stage III-IV, paired lymph node metastasis lesions, and primary tumours with lymph node metastasis (all p < 0.05); and the postoperative survival period of patients with delta-catenin-positive expression was shorter than that of patients with delta-catenin-negative expression (p < 0.05). No competition between delta-catenin and p120ctn for binding to E-cadherin in cytoplasm was found in two lung cancer cell lines. By regulating the activity of small GTPases and changing the cell cycle, delta-catenin could promote the proliferation and invasion of lung cancer cells. We conclude that delta-catenin is an oncoprotein overexpressed in NSCLC and that increased delta-catenin expression is critical for maintenance of the malignant phenotype of lung cancer.
作为连环蛋白家族的一员,关于 δ-连环蛋白在众多肿瘤中的临床意义和可能的机制知之甚少。我们通过免疫组织化学法检测了 115 例非小细胞肺癌(NSCLC)(包括 65 例有随访记录和 50 例配对淋巴结转移病灶)中 δ-连环蛋白的表达。通过 RT-PCR 和 Western blot 分别检测了 30 对肺癌组织和正常肺组织中 δ-连环蛋白的 mRNA 和蛋白表达。采用免疫共沉淀法检测 δ-连环蛋白是否与 p120ctn 在肺癌细胞中竞争结合 E-钙黏蛋白。通过下拉实验、流式细胞术、MTT 和 Matrigel 侵袭实验,探讨了 δ-连环蛋白对小 GTP 酶活性和肺癌细胞生物学行为的影响。结果表明,肺癌组织中 δ-连环蛋白的 mRNA 和蛋白表达增加;腺癌、Ⅲ~Ⅳ期、配对淋巴结转移病灶和原发灶有淋巴结转移患者中 δ-连环蛋白阳性表达率显著升高(均 p<0.05);δ-连环蛋白阳性表达患者的术后生存时间短于 δ-连环蛋白阴性表达患者(p<0.05)。在两种肺癌细胞系中均未发现 δ-连环蛋白与 p120ctn 在细胞质中竞争结合 E-钙黏蛋白。通过调节小 GTP 酶的活性和改变细胞周期,δ-连环蛋白可以促进肺癌细胞的增殖和侵袭。我们得出结论,δ-连环蛋白是 NSCLC 中过度表达的癌蛋白,δ-连环蛋白表达增加对维持肺癌的恶性表型至关重要。