A Combined Gene Expression and Functional Study Reveals the Crosstalk Between N-Myc and Differentiation-inducing MicroRNAs in Neuroblastoma Cells

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dc.contributor.authorZhao, Zhenze
dc.contributor.authorMa, Xiuye
dc.contributor.authorShelton, Spencer D.
dc.contributor.authorSung, Derek C.
dc.contributor.authorLi, Monica
dc.contributor.authorHernandez, Daniel
dc.contributor.authorZhang, Maggie
dc.contributor.authorLosiewicz, Michael D.
dc.contributor.authorChen, Yidong
dc.contributor.authorPertsemlidis, Alexander
dc.contributor.authorYu, Xiaojie
dc.contributor.authorLiu, Yuanhang
dc.contributor.authorDu, Liqin
dc.date.accessioned2020-04-15T19:41:44Z
dc.date.available2020-04-15T19:41:44Z
dc.date.issued2016-10
dc.description.abstractMYCN amplification is the most common genetic alteration in neuroblastoma and plays a critical role in neuroblastoma tumorigenesis. MYCN regulates neuroblastoma cell differentiation, which is one of the mechanisms underlying its oncogenic function. We recently identified a group of differentiation-inducing microRNAs. Given the demonstrated inter-regulation between MYCN and microRNAs, we speculated that MYCN and the differentiation-inducing microRNAs might form an interaction network to control the differentiation of neuroblastoma cells. In this study, we found that eight of the thirteen differentiation-inducing microRNAs, miR-506-3p, miR-124-3p, miR-449a, miR-34a-5p, miR-449b-5p, miR-103a-3p, miR-2110 and miR-34b-5p, inhibit N-Myc expression by either directly targeting the MYCN 3'UTR or through indirect regulations. Further investigation showed that both MYCN-dependent and MYCN-independent pathways play roles in mediating the differentiation-inducing function of miR-506-3p and miR-449a, two microRNAs that dramatically down-regulate MYCN expression. On the other hand, we found that N-Myc inhibits the expression of multiple differentiation-inducing microRNAs, suggesting that these miRNAs play a role in mediating the function of MYCN. In examining the published dataset collected from clinical neuroblastoma specimens, we found that expressions of two miRNAs, miR-137 and miR-2110, were significantly anti-correlated with MYCN mRNA levels, suggesting their interactions with MYCN play a clinically-relevant role in maintaining the MYCN and miRNA expression levels in neuroblastoma. Our findings altogether suggest that MYCN and differentiation-inducing miRNAs form an interaction network that play an important role in neuroblastoma tumorigenesis through regulating cell differentiation.
dc.description.departmentChemistry and Biochemistry
dc.formatText
dc.format.extent16 pages
dc.format.medium1 file (.pdf)
dc.identifier.citationZhao, Z., Ma, X., Shelton, S. D., Sung, D. C., Li, M., Hernandez, D., Zhang, M., Losiewicz, M. D., Chen, Y., Pertsemlidis, A., Yu, X., Liu, Y., & Du, L. (2016). A combined gene expression and functional study reveals the crosstalk between N-Myc and differentiation-inducing microRNAs in neuroblastoma cells. Oncotarget, 7(48), pp. 79358–79373.
dc.identifier.doihttps://doi.org/10.18632/oncotarget.12676
dc.identifier.issn1949-2553
dc.identifier.urihttps://hdl.handle.net/10877/9619
dc.language.isoen
dc.publisherImpact Journals
dc.sourceOncotarget, 2016, Vol. 7, No. 48, pp. 79358–79373.
dc.subjectdifferentiation
dc.subjectmicroRNA
dc.subjectneuroblastoma
dc.subjectMYCN
dc.subjectChemistry and Biochemistry
dc.titleA Combined Gene Expression and Functional Study Reveals the Crosstalk Between N-Myc and Differentiation-inducing MicroRNAs in Neuroblastoma Cells
dc.typeArticle

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