Regulatory Roles of miRNA in the Human Neural Stem Cell Transformation to Glioma Stem Cells. Issue 8 (August 2014)

• Record Type: Journal Article
• Authors: Liu, Shuang; Yin, Feng; Zhang, Jianning; Wicha, Max S.; Chang, Alfred E.; Fan, Wenhong; Chen, Ling; Fan, Ming; Li, Qiao
• Is Part Of: Journal of cellular biochemistry. Volume 115:Issue 8(2014:Aug.)
• Page Start: 1368
• Page End: 1380
• Publication Date: 2014-08
• Subjects: Cytochemistry -- Periodicals; 572
• DOI: 10.1002/jcb.24786
• Languages: English
• ISSNs: 0730-2312

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jcb24786-sec-0001" sec-type="section"> <p>To investigate the expressional alternation of microRNAs (miRNA) during the malignant transformation and development of human glioma, we measured miRNA expression profile as well as mRNA expression profile in normal human neural stem cells (hNSCs) and human glioma stem cells (hGSCs). We found 116 miRNA up‐regulated and 62 miRNA down‐regulated in GSCs. On the other hand, we identified 1, 372 mRNA down‐regulated, and 1, 501 mRNA up‐regulated in GSCs compared to those in NSCs. We then analyzed the pathways and the predicted target genes of the miRNAs which differ significantly in expression between GSCs and NSCs using the statistical enrichment methods. These target mRNAs are involved in many cancer‐related signaling pathways, such as cell cycle, axon guidance, glioma development, adhesion junction, MAPK and Wnt signaling. Furthermore, we obtained the differently expressed miRNA‐target relationships according to the θ value which is used to calculate the regulation extent of miRNA‐target and using the databases of miRanda, Targetscans and Pictar. Among the top 10 miRNA‐target relationships, hsa‐miR‐198 and its potential targeted gene DCX and NNAT were selected for validation, and NNAT was found to be the direct target of miR‐198. Finally, the functional roles of miR‐155–5p and miR‐124–3p whose expressions altered significantly between GSCs and NSCs were addressed. Our results provide new clues for the potential mechanisms involved in the origin and development of glioma. Clinically, the altered miRNAs may serve as potential targets and diagnostic tools for novel therapeutic strategies of glioblastoma. J. Cell. Biochem. 115: 1368–1380, 2014. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract>