Affiliation:
1. Department of Pathology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA
2. Department of Obstetrics and Gynecology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA
Abstract
Molecular profiling of endometrial neoplasms reveals genetic changes in endometrial carcinomas that support the dualistic model, in which type I carcinomas are estrogen-dependent, low grade lesions and type II carcinomas are nonestrogen dependent and high grade. The molecular changes in type I endometrial carcinomas include mutations inPTEN, PIK3CA, KRAS,and -catenin, along with microsatellite instability, whereas type II endometrial carcinomas are characterized by genetic alterations inp53, HER2/neu, p16,and E-cadherin. For endometrial neoplasms with a malignant mesenchymal component,C-MYCmutations and loss of heterozygosity are frequently seen in carcinosarcomas, and a fusion gene,JAZF1/JJAZ1, is distinctive for endometrial stromal sarcoma. In addition,p53mutations may play an important role in tumorigenesis of undifferentiated endometrial sarcoma. These molecular changes can help in the diagnosis of endometrial neoplasms, as well as form the basis of molecular targeted therapy.
Subject
Obstetrics and Gynaecology
Cited by
106 articles.
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