CAJ | 학술논문

目的探讨人黑素瘤细胞株和原代黑素细胞IGFBP7启动子区CpG岛甲基化状态与IGFBP7表达的关系.方法亚硫酸氢钠修饰后测序法检测4株人黑素瘤细胞和原代黑素细胞中IGFBP7基因启动子区CpG岛DNA甲基化状态.结果 IGFBP7表达阴性的3个细胞株(A375、M14、SK-MEL-1)和表达阳性的2个细胞株(MV3及原代黑素细胞)的甲基化模式存在差异,聚类分析各自聚为一类.结论 IGFBP7基因启动子区CpG岛甲基化状态和基因表达有一定相关性.
목적 탐토인흑소류세포주화원대흑소세포IGFBP7계동자구CpG도갑기화상태여IGFBP7표체적관계.방법 아류산경납수식후측서법검측4주인흑소류세포화원대흑소세포중IGFBP7기인계동자구CpG도DNA갑기화상태.결과 IGFBP7표체음성적3개세포주(A375、M14、SK-MEL-1)화표체양성적2개세포주(MV3급원대흑소세포)적갑기화모식존재차이,취류분석각자취위일류.결론 IGFBP7기인계동자구CpG도갑기화상태화기인표체유일정상관성.
Objective To assess the relationship of methylation status of CpG islands in the promoter region of insulin-like growth factor binding protein 7 (IGFBP7) gene with the expression of IGFBP7 gene in human melanoma cell lines and primary melanocytes.Methods Primary melanocytes from human forcskin tissue as well as 4 human melanoma cell lines,including A375,M14,SK-MEL-1 and MV3,were used in this study.Bisulfite sequencing PCR (BSP) was applied to detect the methylation status of 54 CpG sites in the 5'-flanking promoter region of IGFBP7 gene in all of the melanoma cell lines and primary melanocytes.Results As hierarchical cluster analysis showed,IGFBP7-positive cells (including A375,M14 and SK-MEL-1 ) differed significantly from IGFBP7-negative cells (including MV3 cells and primary melanocytes) in the methylation pattern of IGFBP7 gene promoter region.Conclusion The methylation status of CpG island in the promoter region of IGFBP7 gene may be associated with its expression in melanoma cell lines.