Gaedicke G, Drexler H G
Eur J Pediatr. 1984 Aug;142(3):157-64. doi: 10.1007/BF00442441.
Enzyme marker analysis has become a valuable tool in leukemia research, especially as a part of the so-called multiple marker analysis which combines several disciplines for characterization of leukemia cells. In this study the qualitative activities of three enzyme markers were determined in leukemic cells from pediatric patients with acute leukemias: acid phosphatase (E.C. 3.1.3.2), carboxylic esterase (E.C. 3.1.1.1) and hexosaminidase (E.C. 3.2.1.30). The leukemia subtypes displayed different types of isoenzyme patterns. No additional isoenzyme was found that was not observed in normal blood cells, nor a single isoenzyme specific for a leukemia subtype. The biochemical profiles illustrated the existence of subsets in cALL, T-ALL and AML. The enzymologic polymorphism and the immunologic heterogeneity seen in leukemia subclasses have led together to an extended classification scheme of leukemias as well as to model schemes of normal hematopoietic cell differentiation. Despite former and constantly published assumptions there are still no specific markers of leukemia cells.
酶标志物分析已成为白血病研究中的一项重要工具,特别是作为所谓多标志物分析的一部分,该分析结合了多个学科来表征白血病细胞。在本研究中,测定了急性白血病患儿白血病细胞中三种酶标志物的定性活性:酸性磷酸酶(E.C. 3.1.3.2)、羧酸酯酶(E.C. 3.1.1.1)和己糖胺酶(E.C. 3.2.1.30)。白血病亚型表现出不同类型的同工酶模式。未发现正常血细胞中未观察到的额外同工酶,也未发现特定于白血病亚型的单一同工酶。生化图谱说明了普通急性淋巴细胞白血病、T细胞急性淋巴细胞白血病和急性髓细胞白血病中存在亚群。白血病亚类中所见的酶学多态性和免疫异质性共同导致了白血病分类方案的扩展以及正常造血细胞分化的模型方案。尽管以前一直有相关假设发表,但目前仍没有白血病细胞的特异性标志物。