Department of Histology and Embryology, Wroclaw Medical University, Chalubinskiego 6a, 50-368 Wroclaw, Poland.
Anticancer Res. 2013 Dec;33(12):5375-83.
Despite great progress in the understanding of ovarian cancer biology, clinicopathological data (i.e. grade, stage, histological type and residual disease after surgery) seem to be the most important prognostic factors.
The present study aimed to investigate the relationship between expression of minichromosome maintenance proteins (MCM-3, MCM-7), metallothioneins (MT-I/II, MT-III), and Ki-67 in 103 ovarian cancer cases, mostly of the serous histological type.
Statistical analysis revealed strong positive correlations in the expression of MCM-3 vs. Ki-67 (r=0.492), MCM-7 vs. Ki-67 (r=0.651), and MCM-3 vs. MCM-7 (r=0.515) (all p<0.0001). The Kruskal-Wallis test showed an association of increased expression of MCM-3 and Ki-67 with increasing grade of histological malignancy (p=0.0011, p=0.029, respectively). Regarding clinical progression, cytoplasmic MT-I/II expression was significantly higher in more advanced disease stages (III+IV vs. I+II; p=0.0247).
Due to the correlations shown here, the determination of MCM proteins as proliferation markers of ovarian cancer, should be strongly considered.
尽管人们对卵巢癌生物学的认识取得了巨大进展,但临床病理数据(即分级、分期、组织学类型和手术后残留疾病)似乎仍是最重要的预后因素。
本研究旨在探讨 103 例卵巢癌病例(主要为浆液性组织学类型)中微小染色体维持蛋白(MCM-3、MCM-7)、金属硫蛋白(MT-I/II、MT-III)和 Ki-67 的表达与临床病理参数之间的关系。
统计学分析显示,MCM-3 与 Ki-67(r=0.492)、MCM-7 与 Ki-67(r=0.651)以及 MCM-3 与 MCM-7(r=0.515)的表达呈强正相关(均 P<0.0001)。Kruskal-Wallis 检验显示,MCM-3 和 Ki-67 的表达增加与组织学恶性程度的升高相关(P=0.0011,P=0.029)。关于临床进展,细胞质 MT-I/II 的表达在更晚期的疾病阶段(III+IV 期与 I+II 期;P=0.0247)显著更高。
由于这里显示的相关性,强烈考虑将 MCM 蛋白作为卵巢癌增殖标志物的测定。