Whole Exome Sequencing of Growing and Non-Growing Cutaneous Neurofibromas from a Single Patient with Neurofibromatosis Type 1

被引:17
作者
Faden, Daniel L. [1 ]
Asthana, Saurabh [2 ]
Tihan, Tarik [3 ]
DeRisi, Joseph [4 ]
Kliot, Michel [5 ]
机构
[1] Univ Calif San Francisco, Dept Otolaryngol Head & Neck Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Helen Diller Comprehens Canc Ctr, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA
[4] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[5] Northwestern Univ, Dept Neurosurg, Feinberg Sch Med, Chicago, IL 60611 USA
来源
PLOS ONE | 2017年 / 12卷 / 01期
关键词
NF1; GENE; MUTATIONAL SPECTRUM; CANCER; TUMORIGENESIS; EXPRESSION; CHILDREN; TUMORS; RISK;
D O I
10.1371/journal.pone.0170348
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The growth behaviors of cutaneous neurofibromas in patients with Neurofibromatosis type 1 are highly variable. The role of the germline NF1 mutation, somatic NF1 mutation and mutations at modifying loci, are poorly understood. We performed whole exome sequencing of three growing and three non-growing neurofibromas from a single individual to assess the role of acquired somatic mutations in neurofibroma growth behavior. 1-11 mutations were identified in each sample, including two deleterious NF1 mutations. No trends were present between the types of somatic mutations identified and growth behavior. Mutations in the HIPPO signaling pathway appeared to be overrepresented.
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页数:9
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