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PMID: 28068329 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. Research Support, Non-U.S. Gov't Research Support, N.I.H., Intramural

The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas.

Oncogene ·Vol. 36 ·No. 22 ·2017-00-01 ·页码 3168-3177

Pemov A, Li H, Patidar R, Hansen NF, Sindiri S, Hartley SW, Wei JS, Elkahloun A, Chandrasekharappa SC, NISC Comparative Sequencing Program, Boland JF, Bass S, NCI DCEG Cancer Genomics Research Laboratory, Mullikin JC, Khan J, Widemann BC, Wallace MR, Stewart DR

Abstract

Neurofibromatosis type 1 (NF1) is a common tumor-predisposition disorder due to germline mutations in the tumor suppressor gene NF1. A virtually pathognomonic finding of NF1 is the plexiform neurofibroma (PN), a benign, likely congenital tumor that arises from bi-allelic inactivation of NF1. PN can undergo transformation to a malignant peripheral nerve sheath tumor, an aggressive soft-tissue sarcoma. To better understand the non-NF1 genetic contributions to PN pathogenesis, we performed whole-exome sequencing, RNASeq profiling and genome-wide copy-number determination for 23 low-passage Schwann cell cultures established from surgical PN material with matching germline DNA. All resected tumors were derived from routine debulking surgeries. None of the tumors were considered at risk for malignant transformation at the time; for example, there was no pain or rapid growth. Deep (~500X) NF1 exon sequencing was also conducted on tumor DNA. Non-NF1 somatic mutation verification was performed using the Ampliseq/IonTorrent platform. We identified 100% of the germline NF1 mutations and found somatic NF1 inactivation in 74% of the PN. One individual with three PNs had different NF1 somatic mutations in each tumor. The median number of somatic mutations per sample, including NF1, was one (range 0-8). NF1 was the only gene that was recurrently somatically inactivated in multiple tumors. Gene Set Enrichment Analysis of transcriptome-wide tumor RNA sequencing identified five significant (FDR<0.01) and seven trending (0.01⩽FDR<0.02) gene sets related to DNA replication, telomere maintenance and elongation, cell cycle progression, signal transduction and cell proliferation. We found no recurrent non-NF1 locus copy-number variation in PN. This is the first multi-sample whole-exome and whole-transcriptome sequencing study of NF1-associated PN. Taken together with concurrent copy-number data, our comprehensive genetic analysis reveals the primacy of NF1 loss as the driver of PN tumorigenesis.

MeSH 主题词
Carcinogenesis/genetics,metabolism,pathology DNA Replication Gene Dosage Genes, Tumor Suppressor Germ-Line Mutation Humans Neurofibroma, Plexiform/genetics,metabolism,pathology Neurofibromatosis 1/genetics,metabolism,pathology Neurofibromin 1/deficiency,genetics Transcriptome
化学物质
Neurofibromin 1
作者与单位
共 18 位作者,点击展开单位 / ORCID
Pemov A
Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
Li H
Department of Molecular Genetics and Microbiology, UF Genetics Institute, UF Health Cancer Center, University of Florida, Gainesville, FL, USA.
Patidar R
Genetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Hansen N F
Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, Rockville, MD, USA.
Sindiri S
Genetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Hartley S W
Human Genetics Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
Wei J S
Genetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Elkahloun A
Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, Rockville, MD, USA.
Chandrasekharappa S C
Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, Rockville, MD, USA.
NISC Comparative Sequencing Program
Boland J F
Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
Bass S
Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
NCI DCEG Cancer Genomics Research Laboratory
Mullikin J C
Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, Rockville, MD, USA. | NIH Intramural Sequencing Center, National Human Genome Research Institute, Rockville, MD, USA.
Khan J
Genetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Widemann B C
Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Wallace M R
Department of Molecular Genetics and Microbiology, UF Genetics Institute, UF Health Cancer Center, University of Florida, Gainesville, FL, USA.
Stewart D R
Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
1476-5594
Published
2017-00-01
电子出版
2017-00-09
页码
3168-3177
Language
English
Country/Region
England
NLM ID
8711562
基金资助
Intramural NIH HHS · Z01 BC010801-01 · United States
Intramural NIH HHS · Z01 BC010801-02 · United States
NINDS NIH HHS · R29 NS31550 · United States
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