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[Cancer Research 54, 4667-4670, September 1, 1994]
© 1994 American Association for Cancer Research

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Prognostic Significance of p53 Overexpression in Endometrial Cancer1

Kiyoshi Ito2, Keiko Watanabe, Suhail Nasim, Hironobu Sasano, Shinji Sato, Akira Yajima, Steven G. Silverberg and Carleton T. Garrett

Department of Obstetrics and Gynecology [K. I., K. W., S. S., A. Y.] and Pathology [H. S.], Tohoku University School of Medicine, Sendai, Japan, and Department of Pathology, George Washington University Medical Center, Washington, DC 20052 [S. N., S. G. S., C. T. G.]

Abnormalities of p53, a tumor suppressor gene, have been considered to play an important role in tumorigenesis. Clinically, overexpression of p53 has been reported to correlate with poor prognosis in several types of tumors. In this study, we examined 221 cases of endometrioid endometrial carcinoma for overexpression of p53 using immunohistochemistry in patients with a median follow-up of 41 months. Immunohistochemical analysis was performed with monoclonal antibody pAbl801. Overexpression of p53 was detected in 47 of 221 cases (21.3%). There was a statistically significant correlation between p53 overexpression and poor prognosis (P < .0001). In the early stages of cancer (stages 1 and 2), p53 was overexpressed in 11 of 22 patients (50%) who died or had a recurrence during follow-up. In contrast, overexpression was detected in only 14.7% of the 156 disease-free patients during the same period (P < .0001). In advanced stages (stages 3 and 4), tumors from patients with recurrent disease had a higher frequency of overexpression (41.2%; 7 of 17) than those of disease-free patients (23.1%; 6 of 26). However, the difference between these frequencies was not statistically significant. In multivariate analysis using the Cox proportional hazard model, p53 overexpression was an independent risk factor when compared with clinical stage, nuclear grade, and patient age. Our results indicate that p53 immunohistochemical evaluation of the most common form of endometrial cancer may be useful in identifying cases of aggressive carcinoma, especially in the early stages.

1 Supported in part by the National Cancer Institute Grant RO1 CA 47994 and a gift from the Elaine Snyder Research Foundation.

2 To whom requests for reprints should be addressed, at Department of Pathology, Medical College of Virginia, P.O. Box 980662, Richmond, VA 23298-0662.

Received 3/18/94. Accepted 7/ 6/94.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1994 by the American Association for Cancer Research.