Kieslinger Matthias, Swoboda Alexander, Kramer Nina, Freund Patricia, Pratscher Barbara, Neubauer Heidi A, Steinborn Ralf, Wolfesberger Birgitt, Fuchs-Baumgartinger Andrea, Moriggl Richard, Burgener Iwan A
Department for Companion Animals and Horses, Division of Small Animal Internal Medicine, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Department of Biomedical Sciences, Institute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Cancers (Basel). 2021 Oct 19;13(20):5238. doi: 10.3390/cancers13205238.
Alimentary lymphomas arising from T cells are rare and aggressive malignancies in humans. In comparison, they represent the most common anatomical form of lymphoma in cats. Due to the low prevalence in humans, the underlying pathomechanism for these diseases is poorly characterised, limiting experimental analysis and therapeutic exploration. To date, activating mutations of the JAK/STAT core cancer pathway and particularly the STAT5B oncoprotein have been identified in human enteropathy-associated T cell lymphoma. Here, we describe a high homology of human and feline STAT3 and STAT5B proteins and strong conservation at the genomic level. Analysis of 42 samples of feline T cell alimentary lymphoma reveals broad activation of STAT3 and STAT5B. Screening for known activating mutations in or identifies the presence of the driver mutation in feline enteropathy-associated T cell lymphoma in 7 out of 42 (16.67%) samples in total. Regarding lymphoma subtypes, the majority of mutations with 5 out of 17 (29.41%) cases were found in feline enteropathy-associated lymphoma type II (EATL II). This identification of an oncogenic driver mutation in felines recapitulates the genetic situation in the corresponding human disease, thereby establishing the cat as a potential new model for a rare and incurable human T cell disease.
源自T细胞的消化道淋巴瘤在人类中是罕见且侵袭性的恶性肿瘤。相比之下,它们是猫科动物中最常见的淋巴瘤解剖形式。由于在人类中的患病率较低,这些疾病的潜在病理机制特征不明,限制了实验分析和治疗探索。迄今为止,已在人类肠病相关T细胞淋巴瘤中鉴定出JAK/STAT核心癌症通路的激活突变,特别是STAT5B癌蛋白。在此,我们描述了人类和猫科动物STAT3和STAT5B蛋白的高度同源性以及基因组水平的强保守性。对42例猫科动物T细胞消化道淋巴瘤样本的分析显示STAT3和STAT5B广泛激活。对已知激活突变进行筛查,在42个(16.67%)样本中的7个样本中总共鉴定出猫科动物肠病相关T细胞淋巴瘤中存在驱动突变。关于淋巴瘤亚型,17例中有5例(29.41%)的大多数突变见于猫科动物II型肠病相关淋巴瘤(EATL II)。在猫科动物中鉴定出致癌驱动突变再现了相应人类疾病中的遗传情况,从而将猫确立为一种罕见且无法治愈的人类T细胞疾病的潜在新模型。