Ferenc Tomasz, Wroński Jan Wojciech, Kopczyński Janusz, Kulig Andrzej, Sidor Małgorzata, Stalińska Liliana, Dziki Adam, Sygut Jacek
Department of Biology and Genetics, Medical University, Pl. Hallera 1, 90-647 Lodz, Poland.
Pathol Res Pract. 2009;205(5):311-24. doi: 10.1016/j.prp.2008.11.002. Epub 2009 Jan 4.
The aims of this study were to analyze the cadherin/catenin adhesion complex in cells from abdominal and extra-abdominal aggressive fibromatosis tumors, and to estimate the correlation between the expression of the tested proteins and the clinical data of the desmoid patients. Immunohistochemistry was used to examine the expression of the cadherin/catenin adhesion complex: APC protein, alpha-, beta-catenin, and N-cadherin in archival material derived from 15 cases of extra-abdominal desmoid tumor (E-AD) and 20 cases of abdominal (AD) desmoid tumor. The tested proteins demonstrated cytoplasmic (c) staining. Furthermore, nuclear (n) or cytoplasmic and nuclear (c+n) staining was observed for beta-catenin. The mean values of the percentage of positive cells for the tested proteins between E-AD vs. AD did not demonstrate any statistically significant difference except for alpha-catenin. In the E-AD group, in both cases of recurrent tumors, no alpha-catenin expression was observed but the expression of this protein was detected in primary tumors. In the groups investigated, no statistically significant correlation was found between alpha-catenin, beta-catenin (c), (n) and (c+n) expression, and tumor size (p>0.1). The results regarding beta-catenin expression obtained in our study confirm the previous findings that nuclear accumulation of this protein plays a crucial role in the pathogenesis of aggressive fibromatosis.
本研究的目的是分析来自腹部和腹部外侵袭性纤维瘤病肿瘤细胞中的钙黏蛋白/连环蛋白黏附复合体,并评估所检测蛋白质的表达与韧带样瘤患者临床数据之间的相关性。采用免疫组织化学方法检测15例腹部外韧带样瘤(E-AD)和20例腹部韧带样瘤(AD)存档材料中钙黏蛋白/连环蛋白黏附复合体:APC蛋白、α-、β-连环蛋白和N-钙黏蛋白的表达。所检测的蛋白质表现为细胞质(c)染色。此外,β-连环蛋白观察到细胞核(n)或细胞质和细胞核(c+n)染色。除α-连环蛋白外,E-AD与AD之间所检测蛋白质的阳性细胞百分比平均值未显示任何统计学上的显著差异。在E-AD组中,在两例复发性肿瘤中均未观察到α-连环蛋白表达,但在原发性肿瘤中检测到该蛋白的表达。在所研究的组中,未发现α-连环蛋白、β-连环蛋白(c)、(n)和(c+n)表达与肿瘤大小之间存在统计学上的显著相关性(p>0.1)。我们研究中关于β-连环蛋白表达的结果证实了先前的发现,即该蛋白的核积累在侵袭性纤维瘤病的发病机制中起关键作用。