Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma

被引:69
作者
Rettig, Eleni M. [1 ]
Talbot, C. Conover, Jr. [2 ]
Sausen, Mark [3 ]
Jones, Sian [3 ]
Bishop, Justin A. [4 ]
Wood, Laura D. [4 ]
Tokheim, Collin [5 ,6 ]
Niknafs, Noushin [5 ,6 ]
Karchin, Rachel [5 ,6 ,7 ]
Fertig, Elana J. [8 ]
Wheelan, Sarah J. [7 ]
Marchionni, Luigi [7 ]
Considine, Michael [8 ]
Fakhry, Carole [1 ,9 ]
Papadopoulos, Nickolas [10 ,11 ]
Kinzler, Kenneth W. [10 ,11 ]
Vogelstein, Bert [10 ,11 ]
Ha, Patrick K. [1 ,9 ]
Agrawal, Nishant [1 ,10 ,11 ,12 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Inst Basic Biomed Sci, Baltimore, MD USA
[3] Personal Genome Diagnost, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Johns Hopkins Inst Computat Med, Baltimore, MD USA
[6] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD USA
[7] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD USA
[8] Johns Hopkins Univ, Sch Med, Dept Oncol Biostat & Bioinformat, Baltimore, MD USA
[9] Greater Baltimore Med Ctr, Milton J Dance Jr Head & Neck Canc Ctr, Baltimore, MD USA
[10] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Ludwig Ctr Canc Genet & Therapeut, Baltimore, MD 21205 USA
[11] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[12] Univ Chicago, Dept Surg, Sect Otolaryngol Head & Neck Surg, 5841 S Maryland Ave, Chicago, IL 60637 USA
关键词
SQUAMOUS-CELL CARCINOMA; RHO-GTPASES; MYB EXPRESSION; NFIB; HEAD; NECK; GENES; PATHWAY; FUSION; BREAST;
D O I
10.1158/1940-6207.CAPR-15-0316
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adenoid cystic carcinomas (ACC) of the salivary glands are challenging to understand, treat, and cure. To better understand the genetic alterations underlying the pathogenesis of these tumors, we performed comprehensive genome analyses of 25 fresh-frozen tumors, including whole-genome sequencing and expression and pathway analyses. In addition to the well described MYB-NFIB fusion that was found in 11 tumors (44%), we observed five different rearrangements involving the NFIB transcription factor gene in seven tumors (28%). Taken together NFIB translocations occurred in 15 of 25 samples (60%, 95% CI, 41%-77%). In addition, mRNA expression analysis of 17 tumors revealed overexpression of N1218 in ACC tumors compared with normal tissues (P = 0.002). There was no difference in NFIB mRNA expression in tumors with NFIB fusions compared with those without. We also report somatic mutations of genes involved in the axonal guidance and Rho family signaling pathways. Finally, we confirm previously described alterations in genes related to chromatin regulation and Notch signaling. Our findings suggest a separate role for NFIB in ACC oncogenesis and highlight important signaling pathways for future functional characterization and potential therapeutic targeting. Ca nccr Prey Hes; 9(4); 265-74. (C) 2016 AACR.
引用
收藏
页码:265 / 274
页数:10
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