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      Expression of EZH2 and Ki-67 in colorectal cancer and associations with treatment response and prognosis

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          Abstract

          Background:

          Enhancer of zeste homologue 2 (EZH2) is a member of the Polycomb group of genes that is involved in epigenetic silencing and cell cycle regulation.

          Methods:

          We studied EZH2 expression in 409 patients with colorectal cancer stages II and III. The patients were included in a randomised study, and treated with surgery alone or surgery followed by adjuvant chemotherapy.

          Results:

          EZH2 expression was significantly related to increased tumour cell proliferation, as assessed by Ki-67 expression. In colon cancer, strong EZH2 expression ( P=0.041) and high proliferation (⩾40%; P=0.001) were both associated with better relapse-free survival (RFS). In contrast, no such associations were found among rectal cancers. High Ki-67 staining was associated with improved RFS in colon cancer patients who received adjuvant chemotherapy ( P=0.001), but not among those who were treated by surgery alone ( P=0.087). In colon cancers stage III, a significant association between RFS and randomisation group was found in patients with high proliferation ( P=0.046), but not in patients with low proliferation ( P=0.26). Multivariate analyses of colon cancers showed that stage III (hazard ratio (HR) 4.00) and high histological grade (HR 1.80) were independent predictors of reduced RFS, whereas high proliferation indicated improved RFS (HR 0.55).

          Conclusion:

          Strong EZH2 expression and high proliferation are associated features and both indicate improved RFS in colon cancer, but not so in rectal cancer.

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          Most cited references15

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          Levamisole and fluorouracil for adjuvant therapy of resected colon carcinoma.

          Twelve hundred ninety-six patients with resected colon cancer that either was locally invasive (Stage B2) or had regional nodal involvement (Stage C) were randomly assigned to observation or to treatment for one year with levamisole combined with fluorouracil. Patients with Stage C disease could also be randomly assigned to treatment with levamisole alone. The median follow-up time at this writing is 3 years (range, 2 to 5 1/2). Among the patients with Stage C disease, therapy with levamisole plus fluorouracil reduced the risk of cancer recurrence by 41 percent (P less than 0.0001). The overall death rate was reduced by 33 percent (P approximately 0.006). Treatment with levamisole alone had no detectable effect. The results in the patients with Stage B2 disease were equivocal and too preliminary to allow firm conclusions. Toxic effects of levamisole alone were infrequent, usually consisting of mild nausea with occasional dermatitis or leukopenia, and those of levamisole plus fluorouracil were essentially the same as those of fluorouracil alone--i.e., nausea, vomiting, stomatitis, diarrhea, dermatitis, and leukopenia. These reactions were usually not severe and did not greatly impede patients' compliance with their regimen. We conclude that adjuvant therapy with levamisole and fluorouracil should be standard treatment for Stage C colon carcinoma. Since most patients in our study were treated by community oncologists, this approach should be readily adaptable to conventional medical practice.
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            Expression of enhancer of zeste homologue 2 is significantly associated with increased tumor cell proliferation and is a marker of aggressive breast cancer.

            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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              Ki67 protein: the immaculate deception?

              This article updates our previous review of Ki67 published in Histopathology 10 years ago. In this period the numbers of papers published featuring this antibody has increased 10-fold from 338 to 3489 indicating the considerable enthusiasm with which this antibody has been studied. This review attempts to provide an update on the characterization of the Ki67 protein, its function and its use as a prognostic or diagnostic tool.
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                Author and article information

                Journal
                Br J Cancer
                British Journal of Cancer
                Nature Publishing Group
                0007-0920
                1532-1827
                22 September 2009
                13 October 2009
                20 October 2009
                : 101
                : 8
                : 1282-1289
                Affiliations
                [1 ]Department of Oncology, Haukeland University Hospital Bergen, Norway
                [2 ]Department of Pathology, Haukeland University Hospital Bergen, Norway
                [3 ]Department of Surgery, Ullevål University Hospital Oslo, Norway
                [4 ]Department of Surgery, University of Northern Norway Tromsø, Norway
                [5 ]Department of Pathology, Stavanger University Hospital Stavanger, Norway
                [6 ]Laboratory for Pathology AS Oslo, Norway
                [7 ]Department of Pathology, Buskerud Central Hospital Drammen, Norway
                [8 ]Department of Pathology, The National Hospital Oslo, Norway
                [9 ]Department of Pathology, St Olav's Hospital Trondheim, Norway
                [10 ]Department of Oncology, Ullevål University Hospital Oslo, Norway
                [11 ]Department of Biochemistry, Swammerdam Institute for Life Sciences, University of Amsterdam Amsterdam, The Netherlands
                [12 ]The Gade Institute, Department of Pathology, University of Bergen Bergen, Norway
                [13 ]Section of Oncology, Institute of Medicine, University of Bergen Bergen, Norway
                Author notes
                [* ]Author for correspondence: olav.dahl@ 123456helse-bergen.no
                Article
                6605333
                10.1038/sj.bjc.6605333
                2768450
                19773751
                09231c01-950b-4055-b628-04323fb7d0a4
                Copyright 2009, Cancer Research UK
                History
                : 21 April 2009
                : 25 August 2009
                : 25 August 2009
                Categories
                Clinical Studies

                Oncology & Radiotherapy
                ki-76,adjuvant chemotherapy,immunehistochemistry,prediction of outcome,colorectal cancer,ezh2

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