期刊
ONCOGENE
卷 33, 期 45, 页码 5295-5302出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2014.150
关键词
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资金
- Carlos Slim Health Institute in Mexico
- Canadian Institutes of Health Research Fellowship
- National Cancer Institute [R01CA143167]
- National Heart, Lung and Blood Institute [R01HL109265, R01HL111190]
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.
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