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Cancer Epidemiology Biomarkers & Prevention Vol. 15, 1941-1947, October 2006
© 2006 American Association for Cancer Research

Cyclin E Expression and Outcome in Pancreatic Ductal Adenocarcinoma

David A. Skalicky1, James G. Kench1,3, Davendra Segara1, Maxwell J. Coleman2, Robert L. Sutherland1, Susan M. Henshall1, Elizabeth A. Musgrove1 and Andrew V. Biankin1,4

1 Cancer Research Program, Garvan Institute of Medical Research; 2 Division of Surgery, St. Vincent's Clinic; 3 Institute of Clinical Pathology and Medical Research, Westmead Hospital; and 4 Department of Surgery, Bankstown Hospital, Sydney, New South Wales, Australia

Requests for reprints: Davendra Segara, Cancer Research Program, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, Sydney, New South Wales 2010, Australia. Phone: 61-2-9295-8320; Fax: 61-2-9295-8321. E-mail: d.segara{at}garvan.org.au

The association of high cyclin E expression with poor outcome in some cancers, in particular breast cancer, suggests that it may play an important role in tumor biology. Because the influence of cyclin E expression on outcome is yet to be examined in pancreatic cancer, we assessed the relationship between the expression of cyclin E, p27Kip1, and survival in a large cohort of pancreatic cancer patients with long-term follow-up. Expression of cyclin E and p27Kip1 was assessed by immunohistochemistry using tissue microarrays of tumor samples from 118 patients with pancreatic ductal adenocarcinoma (75 resections and 43 biopsies). High cyclin E expression (>10% positive nuclei) was identified in 39 of 118 (33%) patients. This was associated with poor prognosis on univariate analysis in the whole cohort (P = 0.005), as well as in the subgroup of 75 patients who underwent operative resection (P = 0.04). On multivariate analysis, high cyclin E expression was an independent predictor of poor survival in both the entire cohort (P = 0.005) and the resected subgroup (P = 0.03), and was superior to all tested clinicopathologic factors (tumor size, lymph node metastases, differentiation, margin involvement, and perineural invasion) as a marker of survival. Low p27Kip1 expression (<5% positive nuclei) was present in 41 of 111 (37%) patients, but was not associated with survival, and coexpression of p27Kip1 did not influence the association of high cyclin E expression with poor survival. High cyclin E expression is a strong independent predictor of poor outcome in patients with pancreatic cancer. Thus, if these data are confirmed in independent cohorts, measurement of cyclin E may add significant prognostic information to the currently used clinicopathologic variables and hence have potential clinical utility in the management of this disease. (Cancer Epidemiol Biomarkers Prev 2006;15(10):1941–7)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Copyright © 2006 by the American Association for Cancer Research.