Molecular Cancer (Nov 2020)

The PVT1 lncRNA is a novel epigenetic enhancer of MYC, and a promising risk-stratification biomarker in colorectal cancer

  • Kunitoshi Shigeyasu,
  • Shusuke Toden,
  • Tsuyoshi Ozawa,
  • Takatoshi Matsuyama,
  • Takeshi Nagasaka,
  • Toshiaki Ishikawa,
  • Debashis Sahoo,
  • Pradipta Ghosh,
  • Hiroyuki Uetake,
  • Toshiyoshi Fujiwara,
  • Ajay Goel

DOI
https://doi.org/10.1186/s12943-020-01277-4
Journal volume & issue
Vol. 19, no. 1
pp. 1 – 6

Abstract

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Abstract Accumulating evidence suggests that dysregulation of transcriptional enhancers plays a significant role in cancer pathogenesis. Herein, we performed a genome-wide discovery of enhancer elements in colorectal cancer (CRC). We identified PVT1 locus as a previously unrecognized transcriptional regulator in CRC with a significantly high enhancer activity, which ultimately was responsible for regulating the expression of MYC oncogene. High expression of the PVT1 long-non-coding RNA (lncRNA) transcribed from the PVT1 locus was associated with poor survival among patients with stage II and III CRCs (p < 0.05). Aberrant methylation of the PVT1 locus inversely correlated with the reduced expression of the corresponding the PVT1 lncRNA, as well as MYC gene expression. Bioinformatic analyses of CRC-transcriptomes revealed that the PVT1 locus may also broadly impact the expression and function of other key genes within two key CRC-associated signaling pathways – the TGFβ/SMAD and Wnt/β-Catenin pathways. We conclude that the PVT1 is a novel oncogenic enhancer of MYC and its activity is controlled through epigenetic regulation mediated through aberrant methylation in CRC. Our findings also suggest that the PVT1 lncRNA expression is a promising prognostic biomarker and a potential therapeutic target in CRC.

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