CCAT2 , a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer
The University of Texas MD Anderson Cancer Center · Meertens Institute · +22 more institutions
Abstract
The functional roles of SNPs within the 8q24 gene desert in the cancer phenotype are not yet well understood. Here, we report that CCAT2, a novel long noncoding RNA transcript (lncRNA) encompassing the rs6983267 SNP, is highly overexpressed in microsatellite-stable colorectal cancer and promotes tumor growth, metastasis, and chromosomal instability. We demonstrate that MYC, miR-17-5p, and miR-20a are up-regulated by CCAT2 through TCF7L2-mediated transcriptional regulation. We further identify the physical interaction between CCAT2 and TCF7L2 resulting in an enhancement of WNT signaling activity. We show that CCAT2 is itself a WNT downstream target, which suggests the existence of a feedback loop. Finally, we…
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- References
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Authors
53- HLHui LingCorresponding
The University of Texas MD Anderson Cancer Center
- RSRiccardo Spizzo
The University of Texas MD Anderson Cancer Center
- YAYaser Atlasi
Meertens Institute
- MSMilena S. Nicoloso
The University of Texas MD Anderson Cancer Center
- MSMasayoshi Shimizu
The University of Texas MD Anderson Cancer Center
Topics & keywords
- Biology
- Wnt signaling pathway
- Long non-coding RNA
- Genetics
- Colorectal cancer
- TCF7L2
- SNP
- Chromosome instability
- Good health and well-being