Hornef S, Lux J, Rassner G
Universitäts-Hautklinik Tübingen.
Hautarzt. 1992 Feb;43(2):77-80.
The neuron-specific enolase (NSE) level is elevated in neurons and in numerous cells of the APUD system; melanocytes are also considered to belong to this system. In order to test the relevance of NSE as a tumour marker for malignant melanoma, its concentration in serum was radioimmunologically determined in 89 patients with melanomas: 24 in stage I (primary tumours), 44 in stage II (regional metastases), and 21 in stage III (distant metastases). The average (+/- coefficient of variation) concentrations recorded were 7.4 micrograms/l (+/- 46%) in patients in stage I, 5.8 micrograms/l (+/- 32%) in those in stage II, and 11.0 micrograms/l (+/- 72%) in those in stage III. A threshold value of 11.5 micrograms/l was exceeded in 9 cases, including 8 patients in stage III. Since definitely increased values arose almost exclusively in distant metastases, determination of NSE levels in serum is hardly a suitable tool for early detection of latent metastases.
神经元特异性烯醇化酶(NSE)水平在神经元及APUD系统的众多细胞中升高;黑素细胞也被认为属于该系统。为了检测NSE作为恶性黑色素瘤肿瘤标志物的相关性,对89例黑色素瘤患者的血清浓度进行了放射免疫测定:I期(原发性肿瘤)24例,II期(区域转移)44例,III期(远处转移)21例。记录的平均(±变异系数)浓度在I期患者中为7.4微克/升(±46%),II期患者中为5.8微克/升(±32%),III期患者中为11.0微克/升(±72%)。9例超过阈值11.5微克/升,其中包括8例III期患者。由于明显升高的值几乎仅出现在远处转移中,血清NSE水平的测定几乎不是早期检测潜在转移的合适工具。