Pohlodek Kamil, Tan Yen Y, Singer Christian F, Gschwantler-Kaulich Daphne
Second Department of Gynecology and Obstetrics, Faculty of Medicine, Comenius University of Bratislava, 82606 Bratislava, Slovakia.
Department of Obstetrics and Gynecology, Comprehensive Cancer Center, Medical University of Vienna, A-1090 Vienna, Austria.
Oncol Lett. 2016 Dec;12(6):4393-4398. doi: 10.3892/ol.2016.5236. Epub 2016 Oct 10.
Loss of expression of cadherin-11 protein is correlated with a loss of epithelial phenotype and a gain in tumor cell proliferation and invasion. It has been hypothesized that cadherin-11 may be a molecular marker for a more aggressive subtype of breast cancer. The present study examined the expression of the mesenchymal gene/protein cadherin-11 in malignant, benign and healthy breast cancer samples. A paraffin-embedded tissue microarray of both malignant and benign/healthy breast tumor was used. Clinicopathological parameters, including age, grading, tumor size, hormone receptors and HER2 receptors status were obtained from patient medical records. Expression of cadherin-11 was analyzed using the monoclonal mouse anti cadherin-11 IgG2B clone. Total RNA was extracted from each breast cancer sample and subjected to semi-quantitative RT-PCR analysis for cadherin-11. Cadherin-11 was detected in 80/82 malignant breast cancer samples and in 33/70 non-malignant tissue samples. Cadherin-11 expression was observed to be predominantly localized to the membrane of tumor cells. When compared to healthy breast tissue biopsies, both cadherin-11 mRNA and protein were demonstrated to be significantly overexpressed in breast carcinoma (P=0.040 and P<0.0001, respectively). Within malignant tumors, however, protein expression was not identified to be associated with other clinicopathological parameters. Our results indicate that cadherin-11 expression is upregulated in malignant human breast cancer.
钙黏蛋白-11蛋白表达缺失与上皮表型丧失以及肿瘤细胞增殖和侵袭增加相关。据推测,钙黏蛋白-11可能是侵袭性更强的乳腺癌亚型的分子标志物。本研究检测了间充质基因/蛋白钙黏蛋白-11在恶性、良性及健康乳腺癌样本中的表达。使用了恶性和良性/健康乳腺肿瘤的石蜡包埋组织芯片。从患者病历中获取临床病理参数,包括年龄、分级、肿瘤大小、激素受体和HER2受体状态。使用单克隆小鼠抗钙黏蛋白-11 IgG2B克隆分析钙黏蛋白-11的表达。从每个乳腺癌样本中提取总RNA,并对钙黏蛋白-11进行半定量RT-PCR分析。在82例恶性乳腺癌样本中的80例以及70例非恶性组织样本中的33例中检测到钙黏蛋白-11。观察到钙黏蛋白-11表达主要定位于肿瘤细胞膜。与健康乳腺组织活检相比,乳腺癌中钙黏蛋白-11 mRNA和蛋白均显著过表达(分别为P = 0.040和P < 0.0001)。然而,在恶性肿瘤中,未发现蛋白表达与其他临床病理参数相关。我们的结果表明,钙黏蛋白-11表达在人类恶性乳腺癌中上调。