Laboratory of Neuro-oncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Salata 12, Zagreb, Croatia.
Department of Biology, School of Medicine, University of Zagreb, Salata 3, Zagreb, Croatia.
Dis Markers. 2017;2017:9253495. doi: 10.1155/2017/9253495. Epub 2017 Oct 19.
The expression patterns of critical molecular components of Wnt signaling, sFRP3 and DVL3, were investigated in glioblastoma, the most aggressive form of primary brain tumors, with the aim to offer potential biomarkers. The protein expression levels and localizations in tumor tissue were revealed by immunohistochemistry and evaluated by the semiquantitative method and immunoreactivity score. Majority of glioblastomas had moderate expression levels for both DVL3 (52.4%) and sFRP3 (52.3%). Strong expression levels were observed in 23.1% and 36.0% of samples, respectively. DVL3 was localized in cytoplasm in 97% of glioblastomas, of which 44% coexpressed the protein in the nucleus. sFRP3 subcellular distribution showed that it was localized in the cytoplasm in 94% of cases. Colocalization in the cytoplasm and nucleus was observed in 50% of samples. Wilcox test indicated that the domination of the strong signal is in connection with simultaneous localization of DVL3 protein in the cytoplasm and the nucleus. Patients with strong expression of DVL3 will significantly more often have the protein in the nucleus ( = 6.33 × 10). No significant correlation between the two proteins was established, nor were their signal strengths correlated with epidemiological parameters. Our study contributes to better understanding of glioblastoma molecular profile.
我们研究了 Wnt 信号关键分子成分 sFRP3 和 DVL3 在胶质母细胞瘤中的表达模式,旨在寻找潜在的生物标志物。采用免疫组织化学方法检测肿瘤组织中蛋白的表达水平和定位,并采用半定量方法和免疫反应评分进行评估。大多数胶质母细胞瘤的 DVL3(52.4%)和 sFRP3(52.3%)表达水平为中等。分别有 23.1%和 36.0%的样本表达水平较强。97%的胶质母细胞瘤中 DVL3 定位于细胞质,其中 44%的样本同时在核内表达该蛋白。sFRP3 的亚细胞分布表明,94%的病例中其定位于细胞质。50%的样本中观察到细胞质和核内共定位。Wilcox 检验表明,强信号的主导地位与 DVL3 蛋白在细胞质和核内的同时定位有关。DVL3 表达较强的患者核内蛋白表达显著更常见( = 6.33×10)。未发现两种蛋白之间存在显著相关性,其信号强度也与流行病学参数无关。我们的研究有助于更好地了解胶质母细胞瘤的分子特征。