Assessing the miRNA sponge potential of RUNX1T1 in t(8;21) acute myeloid leukemia
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Assessing the miRNA sponge potential of RUNX1T1 in t(8;21) acute myeloid leukemia. / Junge, Alexander; Zandi, Roza; Havgaard, Jakob Hull; Gorodkin, Jan; Cowland, Jack Bernard.
I: Gene, Bind 615, 2017, s. 35-40.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Assessing the miRNA sponge potential of RUNX1T1 in t(8;21) acute myeloid leukemia
AU - Junge, Alexander
AU - Zandi, Roza
AU - Havgaard, Jakob Hull
AU - Gorodkin, Jan
AU - Cowland, Jack Bernard
PY - 2017
Y1 - 2017
N2 - t(8;21) acute myeloid leukemia (AML) is characterized by a translocation between chromosomes 8 and 21 and formation of a distinctive RUNX1-RUNX1T1 fusion transcript. This translocation places RUNX1T1 under control of the RUNX1 promoter leading to a pronounced upregulation of RUNX1T1 transcripts in t(8;21) AML, compared to normal hematopoietic cells. We investigated the role of highly-upregulated RUNX1T1 under the hypothesis that it acts as competing endogenous RNA (ceRNA) titrating microRNAs (miRNAs) away from their target transcripts and thus contributes to AML formation. Using publicly available t(8;21) AML RNA-Seq and miRNA-Seq data available from The Cancer Genome Atlas (TCGA) project, we obtained a network consisting of 605 genes that may act as ceRNAs competing for miRNAs with the suggested RUNX1T1 miRNA sponge. Among the 605 ceRNA candidates, 121 have previously been implied in cancer development. Players in the integrin, cadherin, and Wnt signaling pathways affected by the RUNX1T1 sponge were overrepresented. Finally, among a set of 21 high interest RUNX1T1 ceRNAs we found multiple genes that have previously been linked to AML formation. In conclusion, our study offers a novel look at the role of the RUNX1-RUNX1T1 fusion transcript in t(8;21) AML beyond previously investigated genetic and epigenetic aberrations.
AB - t(8;21) acute myeloid leukemia (AML) is characterized by a translocation between chromosomes 8 and 21 and formation of a distinctive RUNX1-RUNX1T1 fusion transcript. This translocation places RUNX1T1 under control of the RUNX1 promoter leading to a pronounced upregulation of RUNX1T1 transcripts in t(8;21) AML, compared to normal hematopoietic cells. We investigated the role of highly-upregulated RUNX1T1 under the hypothesis that it acts as competing endogenous RNA (ceRNA) titrating microRNAs (miRNAs) away from their target transcripts and thus contributes to AML formation. Using publicly available t(8;21) AML RNA-Seq and miRNA-Seq data available from The Cancer Genome Atlas (TCGA) project, we obtained a network consisting of 605 genes that may act as ceRNAs competing for miRNAs with the suggested RUNX1T1 miRNA sponge. Among the 605 ceRNA candidates, 121 have previously been implied in cancer development. Players in the integrin, cadherin, and Wnt signaling pathways affected by the RUNX1T1 sponge were overrepresented. Finally, among a set of 21 high interest RUNX1T1 ceRNAs we found multiple genes that have previously been linked to AML formation. In conclusion, our study offers a novel look at the role of the RUNX1-RUNX1T1 fusion transcript in t(8;21) AML beyond previously investigated genetic and epigenetic aberrations.
KW - Acute myeloid leukemia
KW - Competing endogenous RNAs
KW - miRNA
KW - Regulatory network
KW - RUNX1T1
KW - t(8;21) AML
U2 - 10.1016/j.gene.2017.03.015
DO - 10.1016/j.gene.2017.03.015
M3 - Journal article
C2 - 28322996
AN - SCOPUS:85016394389
VL - 615
SP - 35
EP - 40
JO - Gene
JF - Gene
SN - 0378-1119
ER -
ID: 184382282