Duncan L M, Deeds J, Hunter J, Shao J, Holmgren L M, Woolf E A, Tepper R I, Shyjan A W
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston 02114, USA.
Cancer Res. 1998 Apr 1;58(7):1515-20.
We have used differential cDNA display to search for genes whose expression correlates with an aggressive phenotype in variants of the B16 murine melanoma line, B16-F1 and B16-F10. This analysis identified a novel gene, termed melastatin, that is expressed at high levels in poorly metastatic variants of B16 melanoma and at much reduced levels in highly metastatic B16 variants. Melastatin was also found to be differentially expressed in tissue sections of human melanocytic neoplasms. Benign nevi express high levels of melastatin, whereas primary melanomas showed variable melastatin expression. Melastatin transcripts were not detected in melanoma metastases. Within the set of human primary cutaneous melanomas examined, melastatin expression appeared to correlate inversely with tumor thickness. The expression pattern observed suggests that loss of melastatin expression is an indicator of melanoma aggressiveness.
我们利用差异cDNA显示技术,在B16小鼠黑色素瘤细胞系的变体B16 - F1和B16 - F10中寻找与侵袭性表型相关的基因表达。该分析鉴定出一个新基因,命名为抑黑素,它在B16黑色素瘤低转移变体中高水平表达,而在高转移的B16变体中表达水平大幅降低。还发现抑黑素在人类黑素细胞肿瘤组织切片中差异表达。良性痣中抑黑素表达水平高,而原发性黑色素瘤中抑黑素表达各异。在黑色素瘤转移灶中未检测到抑黑素转录本。在所检测的人类原发性皮肤黑色素瘤中,抑黑素表达似乎与肿瘤厚度呈负相关。观察到的表达模式表明,抑黑素表达缺失是黑色素瘤侵袭性的一个指标。