Identification of Global DNA Methylation Signatures in Glioblastoma-Derived Cancer Stem Cells. Issue 7 (20th July 2015)

• Record Type: Journal Article
• Authors: Lee, Eun-Joon; Rath, Prakash; Liu, Jimei; Ryu, Dungsung; Pei, Lirong; Noonepalle, Satish K.; Shull, Austin Y.; Feng, Qi; Litofsky, N. Scott; Miller, Douglas C.; Anthony, Douglas C.; Kirk, Mark D.; Laterra, John; Deng, Libin; Xin, Hong-Bo; Wang, Xinguo; Choi, Jeong-Hyeon; Shi, Huidong
• Is Part Of: Journal of genetics and genomics. Volume 42:Issue 7(2015:Jul.)
• Page Start: 355
• Page End: 371
• Publication Date: 2015-07-20
• Subjects: Genetics -- Periodicals; Genomics -- Periodicals; 576.505
• DOI: 10.1016/j.jgg.2015.06.003
• Languages: English
• ISSNs: 1673-8527

Abstract

<abstract xml:lang="en" abstract-type="author" id="abs0010"> <title id="sectitle0010">Abstract</title> <sec> <p id="abspara0010">Glioblastoma (GBM) is the most common and most aggressive primary brain tumor in adults. The existence of a small population of stem-like tumor cells that efficiently propagate tumors and resist cytotoxic therapy is one proposed mechanism leading to the resilient behavior of tumor cells and poor prognosis. In this study, we performed an in-depth analysis of the DNA methylation landscape in GBM-derived cancer stem cells (GSCs). Parallel comparisons of primary tumors and GSC lines derived from these tumors with normal controls (a neural stem cell (NSC) line and normal brain tissue) identified groups of hyper- and hypomethylated genes that display a trend of either increasing or decreasing methylation levels in the order of controls, primary GBMs, and their counterpart GSC lines, respectively. Interestingly, concurrent promoter hypermethylation and gene body hypomethylation were observed in a subset of genes including <italic>MGMT</italic>, <italic>AJAP1</italic> and <italic>PTPRN2</italic>. These unique DNA methylation signatures were also found in primary GBM-derived xenograft tumors indicating that they are not tissue culture-related epigenetic changes. Integration of GSC-specific epigenetic signatures with gene expression analysis further identified candidate tumor suppressor genes that are frequently down-regulated in GBMs such as <italic>SPINT2</italic>, <italic>NEFM</italic> and <italic>PENK</italic>. Forced re-expression of <italic>SPINT2</italic> reduced glioma cell proliferative capacity, anchorage independent growth, cell motility, and tumor sphere formation <italic>in vitro</italic>. The results from this study demonstrate that GSCs possess unique epigenetic signatures that may play important roles in the pathogenesis of GBM.</p> </sec> </abstract>