for the p53 Special Issue
p53 Review Article
TP53 and ovarian cancer†
Article first published online: 24 FEB 2003
DOI: 10.1002/humu.10181
© 2003 Wiley-Liss, Inc.
Issue
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Human Mutation
Special Issue: Focus on p53 and Cancer
Volume 21, Issue 3, pages 285–291, March 2003
Additional Information
How to Cite
Schuijer, M. and Berns, E. M.J.J. (2003), TP53 and ovarian cancer. Hum. Mutat., 21: 285–291. doi: 10.1002/humu.10181
- †
Publication History
- Issue published online: 24 FEB 2003
- Article first published online: 24 FEB 2003
- Abstract
- References
- Cited By
Keywords:
- cancer;
- ovarian cancer;
- TP53;
- histology;
- prognosis;
- BRCA1;
- DPH2L1;
- OVCA1;
- OVCA2;
- tumor suppressor
Abstract
Ovarian cancer represents the fourth most frequent type of cancer among females and is the leading cause of death from gynecological cancer in the western world. This review describes gene alterations in ovarian cancer. Specific emphasis is placed on genetic alterations and the prevalence of TP53 (p53) gene alterations in the distinct biological ovarian tumors (benign, borderline, and malignant) and histological subtypes (serous, mucinous, endometrioid, clear cell), as well as in BRCA1-associated hereditary ovarian cancer. Although multi-modality treatment regimens, including cytoreductive surgery and cisplatin-containing combination chemotherapy, have usefully prolonged survival, the overall cure rate of the disease has not changed dramatically. Ovarian cancer is difficult to eradicate completely by surgery and many patients have only a partial response to postoperative chemotherapy and/or many will develop chemotherapy resistance. All these important factors contribute to the poor prognosis of ovarian cancer patients. In this review, the putative prognostic or predictive value of TP53 in ovarian cancer is addressed. Hum Mutat 21:285–291, 2003. © 2003 Wiley-Liss, Inc.

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