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Exome sequencing of pleuropulmonary blastoma reveals frequent biallelic loss of TP53 and two hits in DICER1 resulting in retention of 5p-derived miRNA hairpin loop sequences

2014; Springer Nature; Volume: 33; Issue: 45 Linguagem: Inglês

10.1038/onc.2014.150

1476-5594

Trevor J. Pugh, Yu Wang, Jian Yang, Amanda L. Field, Lauren Ambrogio, S L Carter, Kristian Cibulskis, Petros Giannikopoulos, Adam Kieżun, J Kim, Aaron McKenna, Elizabeth Nickerson, Gad Getz, S Hoffher, Yoav H. Messinger, Louis P. Dehner, Charles W.M. Roberts, Carlos Rodríguez‐Galindo, Gretchen M. Williams, Christopher Rossi, Matthew Meyerson, D. Ashley Hill,

Metastasis and carcinoma case studies

Pleuropulmonary blastoma is a rare childhood malignancy of lung mesenchymal cells that can remain dormant as epithelial cysts or progress to high-grade sarcoma. Predisposing germline loss-of-function DICER1 variants have been described. We sought to uncover additional contributors through whole exome sequencing of 15 tumor/normal pairs, followed by targeted resequencing, miRNA analysis and immunohistochemical analysis of additional tumors. In addition to frequent biallelic loss of TP53 and mutations of NRAS or BRAF in some cases, each case had compound disruption of DICER1: a germline (12 cases) or somatic (3 cases) loss-of-function variant plus a somatic missense mutation in the RNase IIIb domain. 5p-Derived microRNA (miRNA) transcripts retained abnormal precursor miRNA loop sequences normally removed by DICER1. This work both defines a genetic interaction landscape with DICER1 mutation and provides evidence for alteration in miRNA transcripts as a consequence of DICER1 disruption in cancer.