Otal-Brun M, Webb T E
Cancer Lett. 1979 Jan;6(1):39-44. doi: 10.1016/s0304-3835(79)80018-x.
The activity of uridine kinase, a key enzyme in the salvage pathway for pyrimidine bases and nucleosides and for the activation of the corresponding chemotherapeutic analogs, varied 10-fold in a series of human colon adenosarcomas; similar variations were observed with other tumor types. In contrast to the leukemias where only the adult isozyme appears to be present, both the adult and embryonic forms were present in the solid tumors examined. The qualitative and quantitative differences may account, in part, for differences in the innate (initial) sensitivity of the tumors to pyrimidine base and nucleoside analogs.
尿苷激酶是嘧啶碱基和核苷补救途径以及相应化疗类似物激活过程中的关键酶,其活性在一系列人类结肠腺肉瘤中变化了10倍;在其他肿瘤类型中也观察到了类似的变化。与仅存在成人同工酶的白血病不同,在所检查的实体瘤中同时存在成人型和胚胎型。这些定性和定量差异可能部分解释了肿瘤对嘧啶碱基和核苷类似物的固有(初始)敏感性差异。