Sammarco Alessandro, Gomiero Chiara, Sacchetto Roberta, Beffagna Giorgia, Michieletto Silvia, Orvieto Enrico, Cavicchioli Laura, Gelain Maria Elena, Ferro Silvia, Patruno Marco, Zappulli Valentina
Department of Comparative Biomedicine and Food Science, 9308University of Padua, Italy.
Department of Biomedical Sciences, 9308University of Padua, Italy.
Vet Pathol. 2020 Nov;57(6):774-790. doi: 10.1177/0300985820948823. Epub 2020 Aug 18.
Mammary cancer is a common neoplasm in women, dogs, and cats that still represents a therapeutic challenge. Wnt/β-catenin and Hippo pathways are involved in tumor progression, cell differentiation, and metastasis. The aim of this study was to evaluate mRNA and protein expression of molecules involved in these pathways in human (HBC), canine (CMT), and feline mammary tumors (FMT). Real-time quantitative polymerase chain reaction (qPCR) for , , , , , and , western blotting for YAP, TAZ, and β-catenin, and immunohistochemistry for estrogen receptor (ER), progesterone receptor (PR), ERBB2, β-catenin, and YAP/TAZ were performed on mammary tumor tissues. The protein expression of active β-catenin was higher in tumors than in healthy tissues in all 3 species. The mRNA expression of the downstream gene was increased in HBC ER and CMTs compared to healthy tissues. Membranous and cytoplasmic protein expression of β-catenin were strongly negatively correlated in all 3 species. Tumors showed an increased protein expression of YAP/TAZ when compared to healthy tissues. Notably, YAP/TAZ expression was higher in triple negative breast cancers when compared to HBC ER and in FMTs when compared to CMTs. The mRNA expression of , , , , and was not different between tumors and healthy mammary gland in the 3 species. This study demonstrates deregulation of Wnt/β-catenin and Hippo pathways in mammary tumors, which was more evident at the protein rather than the mRNA level. Wnt/β-catenin and Hippo pathways seem to be involved in mammary carcinogenesis and therefore represent interesting therapeutic targets that should be further investigated.
乳腺癌是女性、犬类和猫类中常见的肿瘤,仍然是一个治疗难题。Wnt/β-连环蛋白和Hippo信号通路参与肿瘤进展、细胞分化和转移。本研究的目的是评估这些信号通路相关分子在人类乳腺癌(HBC)、犬乳腺肿瘤(CMT)和猫乳腺肿瘤(FMT)中的mRNA和蛋白表达。对乳腺肿瘤组织进行了针对 、 、 、 、 和 的实时定量聚合酶链反应(qPCR),针对YAP、TAZ和β-连环蛋白的蛋白质印迹分析,以及针对雌激素受体(ER)、孕激素受体(PR)、ERBB2、β-连环蛋白和YAP/TAZ的免疫组织化学分析。在所有3个物种中,肿瘤中活性β-连环蛋白的蛋白表达均高于健康组织。与健康组织相比,HBC ER和CMT中下游基因 的mRNA表达增加。在所有3个物种中,β-连环蛋白的膜性和细胞质蛋白表达呈强烈负相关。与健康组织相比,肿瘤中YAP/TAZ的蛋白表达增加。值得注意的是,与HBC ER相比,三阴性乳腺癌中YAP/TAZ表达更高,与CMT相比,FMT中YAP/TAZ表达更高。在这3个物种中,肿瘤与健康乳腺组织之间 、 、 、 和 的mRNA表达没有差异。本研究表明,Wnt/β-连环蛋白和Hippo信号通路在乳腺肿瘤中失调,在蛋白水平而非mRNA水平上更为明显。Wnt/β-连环蛋白和Hippo信号通路似乎参与了乳腺癌的发生,因此是值得进一步研究的有趣治疗靶点。