Department of Anatomy, Physiology and Biochemistry, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Alertix Veterinary Diagnostic AB, SE-392 30, Kalmar, Sweden.
BMC Vet Res. 2021 Sep 27;17(1):316. doi: 10.1186/s12917-021-03030-5.
Thymidine kinase 1 (TK1) catalyzes the initial phosphorylation of thymidine in the salvage pathway synthesis of dTTP, an essential building block of DNA. TK1 is a cytosolic enzyme with its highest level during the S-phase of the cell cycle. In cancer cells TK1 is upregulated and excess TK1 is leaked into the blood. Therefore, serum TK1 has been used as biomarker for cancer diagnosis and prognosis in human medicine. Feline TK1 shows high sequence similarity to TK1 from other species. The aim of this study was to characterize feline TK1 and evaluate if serum TK1 can be used as a diagnostic biomarker.
Feline TK1 was cloned, expressed and affinity purified. The purified feline TK1 phosphorylated not only pyrimidine deoxyribonucleosides but also pyrimidine ribonucleosides and to some extent purine deoxynucleosides. A number of anticancer and antiviral nucleoside analogs also served as substrates with fairly high efficiency. ATP and dATP were the preferred phosphate donor. Serum TK1 activity in felines with malignant diseases was significantly higher than that in healthy individuals. ROC analysis revealed an area under the curve (AUC) of 0.98 with a sensitivity of 0.83 and a specificity of 0.95 for felines with lymphoma. Serum TK1 activity in felines with IBD or inflammatory disease was within the same range as healthy ones. Furthermore, in felines with lymphoma serum TK1 activity returned to normal levels in response to treatment.
Feline TK1 has high specific activity and a broader substrate specificity in comparison with TK1 from other species. Serum TK1 activity in felines with malignant diseases is significantly higher than that in normal felines and in felines with inflammatory diseases. These results suggest that serum TK1 may be a promising biomarker for the diagnosis and monitoring of malignant diseases and for the differential diagnosis of certain inflammatory disease.
胸苷激酶 1(TK1)在补救途径合成 dTTP 中催化胸苷的初始磷酸化,dTTP 是 DNA 的基本组成部分。TK1 是一种细胞质酶,在细胞周期的 S 期达到最高水平。在癌细胞中,TK1 上调,过量的 TK1 泄漏到血液中。因此,血清 TK1 已被用作人类医学中癌症诊断和预后的生物标志物。猫科 TK1 与其他物种的 TK1 具有高度的序列相似性。本研究旨在表征猫科 TK1,并评估血清 TK1 是否可作为诊断生物标志物。
克隆、表达和亲和纯化了猫科 TK1。纯化的猫科 TK1 不仅可磷酸化嘧啶脱氧核苷,还可磷酸化嘧啶核糖核苷,并在一定程度上磷酸化嘌呤脱氧核苷。许多抗癌和抗病毒核苷类似物也作为底物,具有相当高的效率。ATP 和 dATP 是优选的磷酸供体。患有恶性疾病的猫科动物的血清 TK1 活性明显高于健康个体。ROC 分析显示,患有淋巴瘤的猫科动物的曲线下面积(AUC)为 0.98,灵敏度为 0.83,特异性为 0.95。患有 IBD 或炎症性疾病的猫科动物的血清 TK1 活性与健康个体相同。此外,患有淋巴瘤的猫科动物在接受治疗后血清 TK1 活性恢复正常。
与其他物种的 TK1 相比,猫科 TK1 的比活性和底物特异性更高。患有恶性疾病的猫科动物的血清 TK1 活性明显高于正常猫科动物和患有炎症性疾病的猫科动物。这些结果表明,血清 TK1 可能是恶性疾病诊断和监测以及某些炎症性疾病鉴别诊断的有前途的生物标志物。