Uva Paolo, Aurisicchio Luigi, Watters James, Loboda Andrey, Kulkarni Amit, Castle John, Palombo Fabio, Viti Valentina, Mesiti Giuseppe, Zappulli Valentina, Marconato Laura, Abramo Francesca, Ciliberto Gennaro, Lahm Armin, La Monica Nicola, de Rinaldis Emanuele
IRBM P Angeletti, Merck MRL-Rome, Pomezia, Italy.
BMC Genomics. 2009 Mar 27;10:135. doi: 10.1186/1471-2164-10-135.
Spontaneous tumors in dog have been demonstrated to share many features with their human counterparts, including relevant molecular targets, histological appearance, genetics, biological behavior and response to conventional treatments. Mammary tumors in dog therefore provide an attractive alternative to more classical mouse models, such as transgenics or xenografts, where the tumour is artificially induced. To assess the extent to which dog tumors represent clinically significant human phenotypes, we performed the first genome-wide comparative analysis of transcriptional changes occurring in mammary tumors of the two species, with particular focus on the molecular pathways involved.
We analyzed human and dog gene expression data derived from both tumor and normal mammary samples. By analyzing the expression levels of about ten thousand dog/human orthologous genes we observed a significant overlap of genes deregulated in the mammary tumor samples, as compared to their normal counterparts. Pathway analysis of gene expression data revealed a great degree of similarity in the perturbation of many cancer-related pathways, including the 'PI3K/AKT', 'KRAS', 'PTEN', 'WNT-beta catenin' and 'MAPK cascade'. Moreover, we show that the transcriptional relationships between different gene signatures observed in human breast cancer are largely maintained in the canine model, suggesting a close interspecies similarity in the network of cancer signalling circuitries.
Our data confirm and further strengthen the value of the canine mammary cancer model and open up new perspectives for the evaluation of novel cancer therapeutics and the development of prognostic and diagnostic biomarkers to be used in clinical studies.
已证明犬类的自发性肿瘤与人类的自发性肿瘤具有许多共同特征,包括相关分子靶点、组织学外观、遗传学、生物学行为以及对传统治疗的反应。因此,犬类乳腺肿瘤为更经典的小鼠模型(如人工诱导肿瘤的转基因或异种移植模型)提供了有吸引力的替代方案。为了评估犬类肿瘤在多大程度上代表具有临床意义的人类表型,我们首次对这两个物种乳腺肿瘤中发生的转录变化进行了全基因组比较分析,特别关注其中涉及的分子途径。
我们分析了来自肿瘤和正常乳腺样本的人类和犬类基因表达数据。通过分析约一万对犬/人类直系同源基因的表达水平,我们观察到与正常对应样本相比,乳腺肿瘤样本中失调的基因存在显著重叠。基因表达数据的通路分析显示,许多癌症相关通路的扰动具有高度相似性,包括“PI3K/AKT”、“KRAS”、“PTEN”、“WNT-β连环蛋白”和“MAPK级联反应”。此外,我们表明在人类乳腺癌中观察到的不同基因特征之间的转录关系在犬类模型中基本得以维持,这表明癌症信号传导网络在种间具有密切的相似性。
我们的数据证实并进一步强化了犬类乳腺癌模型的价值,并为评估新型癌症治疗方法以及开发用于临床研究的预后和诊断生物标志物开辟了新的前景。