Yonemitsu Yutaka, Imazeki Fumio, Chiba Tetsuhiro, Fukai Kenichi, Nagai Yuichiro, Miyagi Satoru, Arai Makoto, Aoki Ryutaro, Miyazaki Masaru, Nakatani Yukio, Iwama Atsushi, Yokosuka Osamu
Department of Medicine and Clinical Oncology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Hum Pathol. 2009 Sep;40(9):1304-11. doi: 10.1016/j.humpath.2009.01.017. Epub 2009 Apr 22.
Polycomb gene products play a crucial role in the development of highly malignant phenotypes and aggressive cancer progression in a variety of cancers; however, their role in hepatocellular carcinoma remains unclear. First, we analyzed the impact of EZH2 and BMI1 modulation on cell growth of HepG2 cells. 3-(4,5-Dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium assays revealed marked growth inhibition after EZH2 or BMI1 knockdown. In addition, simultaneous knockdown of these 2 genes further augmented cell growth inhibitory effects. Next, we conducted immunohistochemical assessment of 86 hepatocellular carcinoma surgical specimens, evaluating the correlation between EZH2 and BMI1 protein expression and clinicopathologic features. High-level EZH2 and BMI1 expression was detected in 57 (66.3%) and 52 tumor tissues (60.5%), respectively. Among these, 48 tumor tissues (55.8%) showed colocalization of EZH2 and BMI1 in almost all tumor cells. The cumulative recurrence rate, but not survival rate, was significantly higher in patients positive for EZH2 (P = .029) and BMI1 (P = .039) than in their negative counterparts, as determined by Kaplan-Meier analysis. These data indicate that EZH2 and BMI1 may cooperate in initiation and progression of hepatocellular carcinoma.
多梳基因产物在多种癌症的高度恶性表型发展和侵袭性癌症进展中发挥关键作用;然而,它们在肝细胞癌中的作用仍不清楚。首先,我们分析了EZH2和BMI1调节对HepG2细胞生长的影响。3-(4,5-二甲基噻唑-2-基)-5-(3-羧甲氧基苯基)-2-(4-磺基苯基)-2H-四唑𬭩测定显示,EZH2或BMI1敲低后有明显的生长抑制。此外,同时敲低这两个基因进一步增强了细胞生长抑制作用。接下来,我们对86例肝细胞癌手术标本进行了免疫组织化学评估,评估EZH2和BMI1蛋白表达与临床病理特征之间的相关性。在57例(66.3%)和52例肿瘤组织(60.5%)中分别检测到高水平的EZH2和BMI1表达。其中,48例肿瘤组织(55.8%)在几乎所有肿瘤细胞中显示EZH2和BMI1共定位。根据Kaplan-Meier分析,EZH2阳性(P = .029)和BMI1阳性(P = .039)患者的累积复发率显著高于阴性患者,而生存率无显著差异。这些数据表明,EZH2和BMI1可能在肝细胞癌的发生和进展中协同作用。