| Literature DB >> 28409421 |
Huifeng Jin1, Jared J Barrott1, Matthew G Cable1, Michael J Monument1, Daniel M Lerman1, Kyllie Smith-Fry1, Dakota Nollner1, Kevin B Jones2,3.
Abstract
Synovial sarcoma (SS) is initiated by a t(X;18) chromosomal translocation and resultant SS18-SSX fusion oncogene. Only a few SS cell lines exist. None has been compared to its source tumor. In order to compare matched tumor and cell line pairs, we performed RNAseq on 3 tumor/cell line pairs from a genetically engineered mouse model of SS, as well as 2 pairs from human SS tumors. Transcriptomes of mouse tumors and derivative cell lines deviated significantly. Differentially expressed genes highlighted inflammatory infiltrates and metabolism. The same was found for the human tumor and cell line pairs. More was shared between different tumors than between any tumor and its cell line. Direct xenografting generated transcriptomes that more closely resembled the primary tumor than did its derivative cell line. SS tumor transcriptomes are powerfully impacted by the environment wherein they reside, especially with regard to immune interaction and metabolism.Entities:
Keywords: GEMM; Microenvironment; RNA transcriptome; Synovial sarcoma
Year: 2017 PMID: 28409421 PMCID: PMC5750196 DOI: 10.1007/s12307-017-0192-y
Source DB: PubMed Journal: Cancer Microenviron ISSN: 1875-2284