Department of Gynecology and Obstetrics, CHRU de Nancy, Nancy, France.
INSERM U954, Université de Lorraine, Vandœuvre-lès-Nancy, France.
Virchows Arch. 2018 Apr;472(4):623-633. doi: 10.1007/s00428-017-2278-9. Epub 2017 Dec 14.
Minichromosome maintenance complex component 6 (MCM6) is involved in initiating DNA replication and is upregulated during licensed G0 phase of the cell cycle. This early expression permits its labeling of more proliferating cells than those by Ki-67. Here using a cohort of 89 endometrioid adenocarcinoma, we report findings made on the prognostic value of MCM6 based on immunohistochemical labeling index (LI) of the protein in comparison with that of Ki67 as no such information is currently available. Additionally, we examined the prognostic values of these markers based on their mRNA expression using a cohort of uterine corpus endometrial carcinoma (UCEC, n = 307) taken from The Cancer Genome Atlas (TCGA) database. Our evidence indicated the presence of a positive correlation between the LI of MCM6 and the histological grade of endometrioid endometrial adenocarcinoma (grade I, 66.7%; grade II, 75.3%; grade III, 81.4%; p < 0.001) and an inverse correlation between the LI of MCM6 and the overall and progression-free survival (p = 0.02 for both). The LI of Ki-67 correlated with grade (p < 0.001), but not survival. The MCM6 and Ki-67 inter-observer intra-class correlation coefficients were excellent: 0.84 (95% confidence interval, 0.83-0.91) and 0.84 (0.77-0.90), respectively. For in silico analyses of the TCGA cohort, both univariate and multivariate Cox analyses (p = 0.003 and p = 0.03, respectively) revealed high MCM6 mRNA Z-scores associated with reduced overall survival. This association was absent for Ki-67. MCM6 is thus a highly reproducible marker of poor prognosis in endometrial cancer. Evaluation of MCM6 should thus be considered in daily practice for risk stratification.
微小染色体维持复合物成分 6(MCM6)参与启动 DNA 复制,并在细胞周期的许可 G0 期上调。这种早期表达允许其标记更多的增殖细胞,而不是 Ki-67 标记的细胞。在这里,我们使用了 89 例子宫内膜样腺癌队列,报告了基于蛋白质免疫组化标记指数(LI)与 Ki-67 相比,MCM6 的预后价值的发现,因为目前尚无此类信息。此外,我们使用来自癌症基因组图谱(TCGA)数据库的子宫体子宫内膜癌(UCEC,n=307)队列检查了这些标志物的预后价值,基于它们的 mRNA 表达。我们的证据表明,MCM6 的 LI 与子宫内膜样腺癌的组织学分级之间存在正相关(I 级,66.7%;II 级,75.3%;III 级,81.4%;p<0.001),而 MCM6 的 LI 与总生存期和无进展生存期呈负相关(p=0.02)。Ki-67 的 LI 与分级相关(p<0.001),但与生存无关。MCM6 和 Ki-67 的观察者间组内相关系数均为优秀:0.84(95%置信区间,0.83-0.91)和 0.84(0.77-0.90)。对于 TCGA 队列的计算分析,单因素和多因素 Cox 分析(p=0.003 和 p=0.03)均显示高 MCM6 mRNA Z 评分与总生存期降低相关。Ki-67 则没有这种关联。因此,MCM6 是子宫内膜癌预后不良的高度可重复标志物。在日常实践中,应考虑评估 MCM6 以进行风险分层。