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Transcriptomic Profiling of 39 Commonly-used Neuroblastoma Cell Lines

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Journal Sci Data
Specialty Science
Date 2017 Mar 29
PMID 28350380
Citations 92
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Abstract

Neuroblastoma cell lines are an important and cost-effective model used to study oncogenic drivers of the disease. While many of these cell lines have been previously characterized with SNP, methylation, and/or mRNA expression microarrays, there has not been an effort to comprehensively sequence these cell lines. Here, we present raw whole transcriptome data generated by RNA sequencing of 39 commonly-used neuroblastoma cell lines. These data can be used to perform differential expression analysis based on a genetic aberration or phenotype in neuroblastoma (e.g., MYCN amplification status, ALK mutation status, chromosome arm 1p, 11q and/or 17q status, sensitivity to pharmacologic perturbation). Additionally, we designed this experiment to enable structural variant and/or long-noncoding RNA analysis across these cell lines. Finally, as more DNase/ATAC and histone/transcription factor ChIP sequencing is performed in these cell lines, our RNA-Seq data will be an important complement to inform transcriptional targets as well as regulatory (enhancer or repressor) elements in neuroblastoma.

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References
1.
Nair P, McArdle L, Cornell J, Cohn S, Stallings R . High-resolution analysis of 3p deletion in neuroblastoma and differential methylation of the SEMA3B tumor suppressor gene. Cancer Genet Cytogenet. 2007; 174(2):100-10. DOI: 10.1016/j.cancergencyto.2006.11.017. View

2.
Kang M, Smith M, Morton C, Keshelava N, Houghton P, Reynolds C . National Cancer Institute pediatric preclinical testing program: model description for in vitro cytotoxicity testing. Pediatr Blood Cancer. 2010; 56(2):239-49. PMC: 3005554. DOI: 10.1002/pbc.22801. View

3.
Bray N, Pimentel H, Melsted P, Pachter L . Near-optimal probabilistic RNA-seq quantification. Nat Biotechnol. 2016; 34(5):525-7. DOI: 10.1038/nbt.3519. View

4.
Vandesompele J, Michels E, De Preter K, Menten B, Schramm A, Eggert A . Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics. Int J Cancer. 2007; 122(5):1177-82. DOI: 10.1002/ijc.23156. View

5.
Ciccarone V, Spengler B, MEYERS M, Biedler J, Ross R . Phenotypic diversification in human neuroblastoma cells: expression of distinct neural crest lineages. Cancer Res. 1989; 49(1):219-25. View