Expression of enhancer of zeste homologue 2 is significantly associated with increased tumor cell proliferation and is a marker of aggressive breast cancer

被引:242
作者
Collett, K
Eide, GE
Arnes, J
Stefansson, IM
Eide, J
Braaten, A
Aas, T
Otte, AP
Akslen, LA [1 ]
机构
[1] Univ Bergen, Haukeland Univ Hosp, Gade Inst, Sect Pathol, N-5021 Bergen, Norway
[2] Univ Bergen, Haukeland Univ Hosp, Clin Res Ctr, N-5021 Bergen, Norway
[3] Univ Bergen, Haukeland Univ Hosp, Dept Radiol, N-5021 Bergen, Norway
[4] Univ Bergen, Haukeland Univ Hosp, Dept Surg, N-5021 Bergen, Norway
[5] Univ Bergen, Dept Publ Hlth & Primary Hlth Care, Sect Epidemiol & Med Stat, N-5021 Bergen, Norway
[6] Univ Amsterdam, Swammerdam Inst Life Sci, Dept Biochem, Amsterdam, Netherlands
关键词
D O I
10.1158/1078-0432.CCR-05-1533
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The polycomb group protein enhancer of zeste homologue 2 (EZH2) has been linked to invasive properties of aggressive breast cancer. In this report, tissue microarray analysis of 190 breast carcinomas from a nested case-control study shows that EZH2 is significantly associated with interval breast cancers. Further, a strong relationship was found with tumor cell proliferation (by Ki-67 expression), locally advanced disease, metastasis at presentation, markers of the basal epithelial phenotype (positivity for cytokeratin 5/6 or P-cadherin), and p53 status. EZH2 expression was also significantly associated with glomeruloid microvascular proliferation, an aggressive angiogenic phenotype. For prediction of aggressive disease (any event of locally advanced disease, lymph node spread, or distant spread), EZH2 was the only variable of significance in multivariate analysis, whereas no additional information was given by Ki-67. Although EZH2 expression was significant in univariate survival analysis, only tumor cell proliferation and lymph node status were significant in the final multivariate model. In conclusion, our findings indicate an important relationship not only between EZH2 and markers of tumor cell proliferation but also with aggressive disease. These findings might be practically important and relevant because the polycomb group proteins have recently been suggested as candidates for targeted therapy.
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收藏
页码:1168 / 1174
页数:7
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