Division of Veterinary Biotechnology, ICAR-Indian Veterinary Research Institute [Deemed University] Izatnagar, Bareilly, UP, India.
Division of Veterinary Surgery, ICAR-Indian Veterinary Research Institute [Deemed University], Izatnagar, Bareilly, UP, India.
Sci Rep. 2018 Oct 25;8(1):15785. doi: 10.1038/s41598-018-34097-0.
Spontaneously occurring canine mammary tumours (CMTs) are the most common neoplasms of female unspayed dogs and are of potential importance as models for human breast cancer as well. Mortality rates are thrice higher in dogs as compared to humans with breast cancer, which can partly be attributed to lack of diagnostic techniques for their early detection. Human breast cancer studies reveal role of autoantibodies in early cancer diagnosis and also the usefulness of autoantibody panels in increasing the sensitivity, as well as, specificity of diagnostic assays. Therefore, in this study, we took advantage of high-throughput Luminex technique for developing a multiplex assay to detect autoantibody signatures against 5 canine mammary tumour-associated autoantigens (TAAs). These TAAs were expressed separately as fusion proteins with halo tag at the N-terminus, which allows easy and specific covalent coupling with magnetic microspheres. The multiplex assay, comprising a panel of candidate autoantigens (TPI, PGAM1, MNSOD, CMYC & MUC1) was used for screening circulating autoantibodies in 125 dog sera samples, including 75 mammary tumour sera and 50 healthy dog sera. The area under curve (AUC) of the combined panel of biomarkers is 0.931 (p < 0.0001), which validates the discriminative potential of the panel in differentiating tumour patients from healthy controls. The assay could be conducted in 3hrs using only 1ul of serum sample and could detect clinical cases of canine mammary tumour with sensitivity and specificity of 78.6% and 90%, respectively. In this study, we report for the first time a multiplexed assay for detection of autoantibodies in canine tumours, utilizing luminex technology and halo-tag coupling strategy. Further to the best of our knowledge, autoantibodies to CMYC and MUC1 have been reported for the first time in canines in this study.
自发性犬乳腺肿瘤(CMTs)是未绝育雌性犬中最常见的肿瘤,并且作为人类乳腺癌的模型也具有潜在的重要性。与患有乳腺癌的人类相比,犬类的死亡率高出三倍,这在一定程度上可以归因于缺乏早期检测的诊断技术。人类乳腺癌研究揭示了自身抗体在早期癌症诊断中的作用,以及自身抗体谱在提高诊断检测的敏感性和特异性方面的有用性。因此,在这项研究中,我们利用高通量 Luminex 技术开发了一种多重检测方法,以检测针对 5 种犬乳腺肿瘤相关自身抗原(TAAs)的自身抗体特征。这些 TAA 分别作为融合蛋白与 N 端的 halo 标签表达,这允许与磁性微球进行简单和特异性的共价偶联。该多重检测方法包括一组候选自身抗原(TPI、PGAM1、MNSOD、CMYC 和 MUC1),用于筛选 125 份犬血清样本中的循环自身抗体,包括 75 份乳腺肿瘤血清和 50 份健康犬血清。该组合生物标志物的曲线下面积(AUC)为 0.931(p<0.0001),验证了该面板在区分肿瘤患者与健康对照方面的区分潜力。该检测方法仅使用 1ul 血清样本即可在 3 小时内完成,并且可以以 78.6%和 90%的灵敏度和特异性检测犬乳腺肿瘤的临床病例。在这项研究中,我们首次报告了一种利用 Luminex 技术和 halo 标签偶联策略检测犬肿瘤自身抗体的多重检测方法。据我们所知,在这项研究中首次报道了 CMYC 和 MUC1 的自身抗体在犬类中存在。