Evaluation of p۵۳, PTEN and β-catenin Immunoexpressions in Primary Ovarian Epithelial Tumors
Publish place: Middle East Journal of Cancer، Vol: 6، Issue: 3
Publish Year: 1394
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
JR_MISJ-6-3_001
تاریخ نمایه سازی: 25 آبان 1402
Abstract:
Background: Ovarian cancer comprises a heterogeneous group of neoplasms. The prognosis cannot be predicted by histopathologic examination alone. The aim of this study is to evaluate p۵۳, PTEN, and β-catenin expressions in primary ovarian carcinomas in an attempt to find a possible relationship with morphologic parameters and clinical findings.Methods: The study included ۱۰۰ epithelial ovarian tumors (borderline and carcinomas) from affiliated hospitals of Shiraz university of medical sciences during ۲۰۰۷-۲۰۱۳. Immunohistochemical staining for p۵۳, PTEN, and β-catenin was performed on ۶۵ serous, ۱۸ mucinous, ۱۰ endometrioid, ۵ clear cell, and ۲ mixed tumors.Results: p۵۳ expression pattern in serous carcinoma significantly differed from endometrioid carcinomas. Strong positivity (۲+) in >۵۰% of the tumor cells favored serous carcinoma. PTEN expression significantly differed in mucinous and serous carcinomas as well as in endometrioid carcinoma and borderline endometrioid tumor. There was significantly decreased β-catenin expression in the carcinomas compared with borderline tumors. In all of the different subtypes of ovarian carcinomas, we observed a significant association with decreased β-catenin expression to tumor grade as well as in serous carcinomas with increased nuclear grade, mitosis, and tumor grade. There was no significant relation between expressions of p۵۳, PTEN, and β-catenin in epithelial ovarian tumors to FIGO staging, response to chemotherapy, serum CA- ۱۲۵ marker, and tumor recurrence.Conclusion: p۵۳ and PTEN are helpful in differentiation of some epithelial ovarian tumor subtypes. In serous carcinomas, diminished expression of β-catenin is associated with higher tumor and nuclear grade. This expression is significantly different in borderline and carcinomas.
Authors
Fatemeh Sari Aslani
Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran
Azarmidokht Momeni
Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran
Mozhdeh Momtahan
Department of Obstetrics and Gynecology, Shiraz University of Medical Sciences, Shiraz, Iran
Mozhgan Akbarzadeh Jahromi
Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran
Amir Reza Dehghanian
Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran
Dorna Motevali
Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran