Rummel M M, Sers C, Johnson J P
Institute for Immunology, Ludwig-Maximilians University, Munich, Germany.
Cancer Res. 1996 May 1;56(9):2218-23.
MUC18/MCAM is a melanoma-associated cell adhesion molecule that is also occasionally found on carcinomas and other tumor types. On melanomas, MUC18 expression increases with tumor progression and is found on more than 70% of metastatic lesions. To investigate the regulation of MUC18 expression, cell lines of diverse tissue origin were exposed to cytokines, regulators of intracellular cyclic AMP (cAMP), and to phorbol ester. MUC18 expression could not be induced in negative cell lines and could only be modulated by changes in cAMP levels or by exposure to phorbol ester in positive cells. An increase in intracellular cAMP led to an up-regulation in cell surface MUC18 that was maximal at 48 h. Increased MUC18 mRNA levels were observed as soon as 4 h and were 3-fold higher than in control cells by 48 h. Exposure of the cells to phorbol ester reduced MUC18 surface expression to background levels by 24 h. This downregulation was associated with decreased mRNA levels that were apparent at 8 h. By 24 h, steady-state levels of MUC18 mRNA had been reduced by 58%. Whereas similar changes in MUC18 surface expression were observed in MUC18-expressing glioma and carcinoma cell lines, melanoma cells were more resistant to the MUC18-modulating effects of cAMP analogues and phorbol ester. These observations suggest that the strong MUC18 expression observed in advanced melanomas may reflect disturbances in the normal regulation of this molecule.
MUC18/MCAM是一种与黑色素瘤相关的细胞粘附分子,偶尔也会在癌和其他肿瘤类型中发现。在黑色素瘤中,MUC18的表达随着肿瘤进展而增加,并且在超过70%的转移病灶中可以检测到。为了研究MUC18表达的调控机制,将不同组织来源的细胞系暴露于细胞因子、细胞内环状AMP(cAMP)调节剂和佛波酯中。在阴性细胞系中无法诱导MUC18的表达,而在阳性细胞中,MUC18的表达只能通过cAMP水平的变化或暴露于佛波酯来调节。细胞内cAMP的增加导致细胞表面MUC18上调,在48小时时达到最大值。在4小时时即可观察到MUC18 mRNA水平升高,到48小时时比对照细胞高3倍。将细胞暴露于佛波酯中,24小时后MUC18表面表达降低至背景水平。这种下调与8小时时明显降低的mRNA水平相关。到24小时时,MUC18 mRNA的稳态水平降低了58%。尽管在表达MUC18的胶质瘤和癌细胞系中观察到了类似的MUC18表面表达变化,但黑色素瘤细胞对cAMP类似物和佛波酯的MUC18调节作用更具抗性。这些观察结果表明,在晚期黑色素瘤中观察到的强烈MUC18表达可能反映了该分子正常调控的紊乱。