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Targeted genomic profiling reveals recurrent KRASmutations and gain of chromosome 1q in mesonephric carcinomas of the female genital tract

Authors :
Mirkovic, Jelena
Sholl, Lynette M
Garcia, Elizabeth
Lindeman, Neal
MacConaill, Laura
Hirsch, Michelle
Dal Cin, Paola
Gorman, Melissa
Barletta, Justine A
Nucci, Marisa R
McCluggage, W Glenn
Howitt, Brooke E
Source :
Modern Pathology; November 2015, Vol. 28 Issue: 11 p1504-1514, 11p
Publication Year :
2015

Abstract

Mesonephric carcinoma is a rare form of gynecologic cancer derived from mesonephric remnants usually located in the lateral wall of the uterine cervix. An analogous tumor occurs in the adnexa, female adnexal tumor of probable Wolffian origin. The pathogenesis and molecular events in mesonephric carcinoma are not known. The aim of this study was to examine the molecular alterations in mesonephric carcinoma to identify driver mutations and therapeutically targetable mutations. This study consisted of 19 tumors from 17 patients: 18 mesonephric carcinomas (15 primary tumors and three metastatic tumors) and 1 female adnexal tumor of probable Wolffian origin. In two patients, both primary and metastatic tumors were available. Genomic DNA was isolated and targeted next-generation sequencing was performed to detect mutations, copy number variations, and structural variants by surveying full exonic regions of 300 cancer genes and 113 selected intronic regions across 35 genes. Fluorescence in situhybridization (FISH) for 1p and 1q was performed in two cases. Eighty-one percent (13/16) of mesonephric carcinomas had either a KRAS(n=12) or NRAS(n=1) mutation. Mutations in chromatin remodeling genes (ARID1A, ARID1B, or SMARCA4) were present in 62% of mesonephric carcinomas. All mesonephric carcinomas lacked mutations in PIK3CAand PTEN. The most common copy number alteration was 1q gain, found in 12 (75%) mesonephric carcinomas; this was confirmed by FISH in two cases. Mesonephric carcinoma is characterized by molecular alterations that differ from those of more common variants of cervical and endometrial adenocarcinoma, which harbor KRAS/NRASmutations in 7% and 25% of cases, respectively. KRAS/NRASmutations are common in mesonephric carcinoma and are often accompanied by gain of 1q and mutations in chromatin remodeling genes. Targeting inhibitors of the RAS/MAPK pathway may be useful in the treatment of mesonephric carcinoma.

Details

Language :
English
ISSN :
08933952 and 15300285
Volume :
28
Issue :
11
Database :
Supplemental Index
Journal :
Modern Pathology
Publication Type :
Periodical
Accession number :
ejs62057632
Full Text :
https://doi.org/10.1038/modpathol.2015.103