Brot Simone de, Cobb Jack, Alibhai Aziza A, Jackson-Oxley Jorja, Haque Maria, Patke Rodhan, Harris Anna E, Woodcock Corinne L, Lothion-Roy Jennifer, Varun Dhruvika, Thompson Rachel, Gomes Claudia, Kubale Valentina, Dunning Mark D, Jeyapalan Jennie N, Mongan Nigel P, Rutland Catrin S
School of Veterinary Medicine and Science, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Comparative Pathology Platform of the University of Bern (COMPATH), Institute of Animal Pathology, University of Bern, 3012 Bern, Switzerland.
Cancers (Basel). 2024 May 20;16(10):1945. doi: 10.3390/cancers16101945.
Osteosarcoma (OSA) is the most common type of primary bone malignancy in people and dogs. Our previous molecular comparisons of canine OSA against healthy bone resulted in the identification of differentially expressed protein-expressing genes (forkhead box protein O4 (), interferon regulatory factor 8 (), and lymphoid enhancer binding factor 1 ()). Immunohistochemistry (IHC) and H-scoring provided semi-quantitative assessment of nuclear and cytoplasmic staining alongside qualitative data to contextualise staining ( = 26 patients). FOXO4 was expressed predominantly in the cytoplasm with significantly lower nuclear H-scores. IRF8 H-scores ranged from 0 to 3 throughout the cohort in the nucleus and cytoplasm. LEF1 was expressed in all patients with significantly lower cytoplasmic staining compared to nuclear. No sex or anatomical location differences were observed. While reduced levels of FOXO4 might indicate malignancy, the weak or absent protein expression limits its primary use as diagnostic tumour marker. IRF8 and LEF1 have more potential for prognostic and diagnostic uses and facilitate further understanding of their roles within their respective molecular pathways, including Wnt/beta-catenin/LEF1 signalling and differential regulation of tumour suppressor genes. Deeper understanding of the mechanisms involved in OSA are essential contributions towards the development of novel diagnostic, prognostic, and treatment options in human and veterinary medicine contexts.
骨肉瘤(OSA)是人和犬中最常见的原发性骨恶性肿瘤类型。我们之前对犬骨肉瘤与健康骨骼进行的分子比较,鉴定出了差异表达的蛋白质表达基因(叉头框蛋白O4()、干扰素调节因子8()和淋巴样增强子结合因子1())。免疫组织化学(IHC)和H评分提供了核染色和细胞质染色的半定量评估以及定性数据,以对染色情况进行背景分析(=26例患者)。FOXO4主要在细胞质中表达,核H评分显著较低。在整个队列中,IRF8在细胞核和细胞质中的H评分范围为0至3。LEF1在所有患者中均有表达,与细胞核相比,细胞质染色显著较低。未观察到性别或解剖位置差异。虽然FOXO4水平降低可能表明存在恶性肿瘤,但蛋白质表达微弱或缺失限制了其作为诊断肿瘤标志物的主要用途。IRF8和LEF1在预后和诊断方面有更大的应用潜力,有助于进一步了解它们在各自分子途径中的作用,包括Wnt/β-连环蛋白/LEF1信号传导以及肿瘤抑制基因的差异调节。深入了解骨肉瘤所涉及的机制对于在人类和兽医学背景下开发新的诊断、预后和治疗方案至关重要。