Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
Department of Radiology and Oncology, School of Medicine, University of São Paulo, São Paulo, Brazil; ICESP - Cancer Institute of the State of São Paulo, São Paulo, Brazil.
Gynecol Oncol. 2018 Sep;150(3):545-551. doi: 10.1016/j.ygyno.2018.06.014. Epub 2018 Jun 28.
The methylation profile of genes in precursor lesions in cervical cancer was characterized to improve screening techniques for high-grade intraepithelial neoplasia.
A total of 447 cervical cytology samples obtained from women who underwent colposcopy were examined. The cases were distributed as follows: (1) cervices without cervical intraepithelial neoplasia (CIN; n = 152); (2) cervices with a CIN grade of 1 (CIN 1; n = 147); and (3) cervices with a CIN grade of 2 or 3 (CIN 2/3; n = 148). The methylation pattern for a panel of 15 genes was analysed by quantitative methylation-specific PCR (qMSP) and compared between the groups (≤CIN 1 vs. CIN 2+).
In the validation set, seven genes presented significantly different methylation profiles according to diagnosis, namely, DAPK1 (p = 0.001), EPB41L3 (p = 0.001), HIC1 (p = 0.028), hsa-miR-124-2 (p = 0.001), LMX1A (p = 0.001), SOX1 (p = 0.001), and TERT (p = 0.001). Six genes showed a significant increase in the frequency of methylation in the presence of hr-HPV, namely, DAPK1 (p = 0.001), EPB41L3 (p = 0.001), hsa-miR-124-2 (p = 0.001), LMX1A (p = 0.001), SOX1 (p = 0.001), and TERT (p = 0.001). The methylation of the hsa-miR-124 gene showed sensitivity and specificity (86.7% and 61.3%, respectively) similar to that of the HPV test (91.3% and 50.0%, respectively). The independent factors associated with the diagnosis of CIN 2+ and the methylation of the hsa-miR-124-2 (OR = 5.1), SOX1 (OR = 2.8), TERT (OR = 2.2), and LMX1A (OR = 2.0) genes were a positive test for hr-HPV (odds ratio [OR] = 5.5).
Hypermethylation of the hsa-miR-124-2, SOX1, TERT, and LMX1A genes may be a promising biomarker for precursor lesions in cervical cancer regardless of the hr-HPV status.
对宫颈癌前病变基因的甲基化谱进行分析,以改善高级别上皮内瘤变的筛查技术。
共检测了 447 例接受阴道镜检查的女性的宫颈细胞学样本。病例分布如下:(1)无宫颈上皮内瘤变(CIN)的宫颈(n=152);(2)CIN 1 级宫颈(n=147);和(3)CIN 2/3 级宫颈(n=148)。采用定量甲基化特异性 PCR(qMSP)分析一组 15 个基因的甲基化模式,并比较各组间的差异(≤CIN 1 与 CIN 2+)。
在验证集中,根据诊断结果,有七个基因呈现出明显不同的甲基化谱,分别为 DAPK1(p=0.001)、EPB41L3(p=0.001)、HIC1(p=0.028)、hsa-miR-124-2(p=0.001)、LMX1A(p=0.001)、SOX1(p=0.001)和 TERT(p=0.001)。在存在高危型 HPV 的情况下,有六个基因的甲基化频率显著增加,分别为 DAPK1(p=0.001)、EPB41L3(p=0.001)、hsa-miR-124-2(p=0.001)、LMX1A(p=0.001)、SOX1(p=0.001)和 TERT(p=0.001)。hsa-miR-124 基因的甲基化具有与 HPV 检测相似的敏感性和特异性(分别为 86.7%和 61.3%)。与 CIN 2+诊断和 hsa-miR-124-2、SOX1、TERT 和 LMX1A 基因甲基化相关的独立因素是 hr-HPV 的阳性检测(比值比[OR]分别为 5.1、2.8、2.2 和 2.0)。
hsa-miR-124-2、SOX1、TERT 和 LMX1A 基因的高甲基化可能是一种有前途的宫颈癌前病变生物标志物,与 hr-HPV 状态无关。