| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2039539 | Cell Reports | 2016 | 9 Pages |
•We identify a Wnt-regulated long non-coding RNA, WiNTRLINC1•Its downregulation in colon cancer cells causes growth defects and induces apoptosis•It positively regulates ASCL2 through long-distance looping and chromatin changes•The WiNTRLINC1-ASCL2 regulatory axis is amplified in colorectal cancer
SummaryThe canonical Wnt pathway plays a central role in stem cell maintenance, differentiation, and proliferation in the intestinal epithelium. Constitutive, aberrant activity of the TCF4/β-catenin transcriptional complex is the primary transforming factor in colorectal cancer. We identify a nuclear long non-coding RNA, termed WiNTRLINC1, as a direct target of TCF4/β-catenin in colorectal cancer cells. WiNTRLINC1 positively regulates the expression of its genomic neighbor ASCL2, a transcription factor that controls intestinal stem cell fate. WiNTRLINC1 interacts with TCF4/β-catenin to mediate the juxtaposition of its promoter with the regulatory regions of ASCL2. ASCL2, in turn, regulates WiNTRLINC1 transcriptionally, closing a feedforward regulatory loop that controls stem cell-related gene expression. This regulatory circuitry is highly amplified in colorectal cancer and correlates with increased metastatic potential and decreased patient survival. Our results uncover the interplay between non-coding RNA-mediated regulation and Wnt signaling and point to the diagnostic and therapeutic potential of WiNTRLINC1.
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