Giuliano Antonio, Swift Rebecca, Arthurs Callum, Marote Georgina, Abramo Francesca, McKay Jenny, Thomson Calum, Beltran Mariana, Millar Michael, Priestnall Simon, Dobson Jane, Costantino-Casas Fernando, Petrou Terry, McGonnell Imelda M, Davies Anthony J, Weetman Malcolm, Garden Oliver A, Masters John R, Thrasivoulou Christopher, Ahmed Aamir
Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
Department of Clinical Sciences and Services, The Royal Veterinary College, London, United Kingdom.
PLoS One. 2016 Aug 25;11(8):e0161103. doi: 10.1371/journal.pone.0161103. eCollection 2016.
Feline oral squamous cell carcinoma (FOSCC) is an aggressive neoplasm in cats. Little is known about the possible molecular mechanisms that may be involved in the initiation, maintenance and progression of FOSCC. Wnt signalling is critical in development and disease, including many mammalian cancers. In this study, we have investigated the expression of Wnt signalling related proteins using quantitative immunohistochemical techniques on tissue arrays. We constructed tissue arrays with 58 individual replicate tissue samples. We tested for the expression of four key Wnt/ß-catenin transcription targets, namely Cyclin D1 (CCND1 or CD1), FRA1, c-Myc and MMP7. All antibodies showed cross reactivity in feline tissue except MMP7. Quantitative immunohistochemical analysis of single proteins (expressed as area fraction / amount of tissue for normal vs tumor, mean ± SE) showed that the expression of CD1 (3.9 ± 0.5 vs 12.2 ± 0.9), FRA1 (5.5 ± 0.6 vs 16.8 ± 1.1) and c-Myc (5.4 ± 0.5 vs 12.5 ± 0.9) was increased in FOSCC tissue by 2.3 to 3 fold compared to normal controls (p<0.0001). By using a multilabel, quantitative fluorophore technique we further investigated if the co-localization of these proteins (all transcription factors) with each other and in the nucleus (stained with 4',6-diamidino-2-phenylindole, DAPI) was altered in FOSCC compared to normal tissue. The global intersection coefficients, a measure of the proximity of two fluorophore labeled entities, showed that there was a significant change (p < 0.01) in the co-localization for all permutations (e.g. CD1/FRA1 etc), except for the nuclear localization of CD1. Our results show that putative targets of Wnt signalling transcription are up-regulated in FOSCC with alterations in the co-localization of these proteins and could serve as a useful marker for the disease.
猫口腔鳞状细胞癌(FOSCC)是猫的一种侵袭性肿瘤。对于可能参与FOSCC起始、维持和进展的分子机制知之甚少。Wnt信号在发育和疾病中至关重要,包括许多哺乳动物癌症。在本研究中,我们使用定量免疫组织化学技术在组织芯片上研究了Wnt信号相关蛋白的表达。我们构建了包含58个单独重复组织样本的组织芯片。我们检测了四个关键的Wnt/β-连环蛋白转录靶点的表达,即细胞周期蛋白D1(CCND1或CD1)、FRA1、c-Myc和基质金属蛋白酶7(MMP7)。除MMP7外,所有抗体在猫组织中均显示出交叉反应性。对单个蛋白的定量免疫组织化学分析(表示为正常组织与肿瘤组织的面积分数/组织量,平均值±标准误)显示,与正常对照相比,FOSCC组织中CD1(3.9±0.5对12.2±0.9)、FRA1(5.5±0.6对16.8±1.1)和c-Myc(5.4±0.5对12.5±0.9)的表达增加了2.3至3倍(p<0.0001)。通过使用多标记定量荧光技术,我们进一步研究了与正常组织相比,这些蛋白(所有转录因子)在FOSCC中彼此之间以及在细胞核中(用4',6-二脒基-2-苯基吲哚,DAPI染色)的共定位是否发生改变。全局交叉系数是衡量两个荧光团标记实体接近程度的指标,结果显示除CD1的核定位外,所有排列组合(如CD1/FRA1等)的共定位均有显著变化(p<0.01)。我们的结果表明,Wnt信号转录的假定靶点在FOSCC中上调,且这些蛋白的共定位发生改变,可作为该疾病的有用标志物。