De Araújo Érica S S, Kashiwabara André Y, Achatz Maria I W, Moredo Luciana F, De Sá Bianca C S, Duprat João P, Rosenberg Carla, Carraro Dirce M, Krepischi Ana C V
aInternational Research Center bDepartment of Oncogenetics cSkin Cancer Department, A. C. Camargo Cancer Center dDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo eFederal Technological University of Paraná, Paraná, Brazil.
Melanoma Res. 2015 Apr;25(2):173-7. doi: 10.1097/CMR.0000000000000141.
Aberrant DNA methylation pattern is a well-known epigenetic marker of cancer cells. Recently, aberrant methylation was also reported in the peripheral blood of cancer patients and it could potentially serve as a biomarker for cancer risk. We investigated the methylation pattern of LINE-1 and other repetitive DNA elements in peripheral blood of cutaneous melanoma patients in order to search for an association with clinical characteristics. The patient cohort was composed by 69 unrelated melanoma patients, 28 of whom were hereditary cases (with or without CDKN2A mutations) and 41 were isolated (sporadic) melanoma cases. Methylation of LINE-1 was evaluated by pyrosequencing, whereas additional repetitive DNA sequences were assessed using Illumina 450K methylation microarray. Melanoma patients exhibited a higher, albeit heterogeneous, LINE-1 methylation level compared with controls. Hereditary melanoma patients carrying CDKN2A mutations showed a hypermethylated pattern of both LINE-1 and repetitive DNA elements compared with other patients. In particular, the methylation level at one specific CpG of LINE-1 was found to be correlated with the occurrence of metastasis. Our data suggest that LINE-1 hypermethylation in peripheral blood of melanoma patients is a potential epigenetic biomarker for metastasis occurrence.
异常的DNA甲基化模式是癌细胞一种众所周知的表观遗传标记。最近,癌症患者外周血中也报道了异常甲基化,它有可能作为癌症风险的生物标志物。我们研究了皮肤黑色素瘤患者外周血中LINE-1和其他重复DNA元件的甲基化模式,以寻找与临床特征的关联。患者队列由69名无亲缘关系的黑色素瘤患者组成,其中28例为遗传性病例(有或无CDKN2A突变),41例为散发性黑色素瘤病例。通过焦磷酸测序评估LINE-1的甲基化,而使用Illumina 450K甲基化微阵列评估其他重复DNA序列。与对照组相比,黑色素瘤患者的LINE-1甲基化水平更高,尽管存在异质性。与其他患者相比,携带CDKN2A突变的遗传性黑色素瘤患者的LINE-1和重复DNA元件均呈现高甲基化模式。特别是,发现LINE-1一个特定CpG位点的甲基化水平与转移的发生相关。我们的数据表明,黑色素瘤患者外周血中LINE-1的高甲基化是转移发生的潜在表观遗传生物标志物。