miR-508 Defines the Stem-like/Mesenchymal Subtype in Colorectal Cancer

Cancer Res. 2018 Apr 1;78(7):1751-1765. doi: 10.1158/0008-5472.CAN-17-2101. Epub 2018 Jan 26.

Abstract

Colorectal cancer includes an invasive stem-like/mesenchymal subtype, but its genetic drivers, functional, and clinical relevance are uncharacterized. Here we report the definition of an altered miRNA signature defining this subtype that includes a major genomic loss of miR-508. Mechanistic investigations showed that this miRNA affected the expression of cadherin CDH1 and the transcription factors ZEB1, SALL4, and BMI1. Loss of miR-508 in colorectal cancer was associated with upregulation of the novel hypoxia-induced long noncoding RNA AK000053. Ectopic expression of miR-508 in colorectal cancer cells blunted epithelial-to-mesenchymal transition (EMT), stemness, migration, and invasive capacity in vitro and in vivo In clinical colorectal cancer specimens, expression of miR-508 negatively correlated with stemness and EMT-associated gene expression and positively correlated with patient survival. Overall, our results showed that miR-508 is a key functional determinant of the stem-like/mesenchymal colorectal cancer subtype and a candidate therapeutic target for its treatment.Significance: These results define a key functional determinant of a stem-like/mesenchymal subtype of colorectal cancers and a candidate therapeutic target for its treatment. Cancer Res; 78(7); 1751-65. ©2018 AACR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Caco-2 Cells
  • Cadherins / biosynthesis
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / pathology*
  • Epithelial-Mesenchymal Transition / genetics*
  • HCT116 Cells
  • HT29 Cells
  • Humans
  • Lung Neoplasms / secondary
  • Mesenchymal Stem Cells / cytology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred NOD
  • Mice, Nude
  • Mice, SCID
  • MicroRNAs / genetics*
  • Neoplasm Invasiveness / genetics
  • Neoplasm Transplantation
  • Polycomb Repressive Complex 1 / biosynthesis
  • RNA, Long Noncoding / biosynthesis
  • RNA, Long Noncoding / genetics
  • Transcription Factors / biosynthesis
  • Transplantation, Heterologous
  • Zinc Finger E-box-Binding Homeobox 1 / biosynthesis

Substances

  • Antigens, CD
  • BMI1 protein, human
  • CDH1 protein, human
  • Cadherins
  • MIRN508 microRNA, human
  • MicroRNAs
  • RNA, Long Noncoding
  • SALL4 protein, human
  • Transcription Factors
  • ZEB1 protein, human
  • Zinc Finger E-box-Binding Homeobox 1
  • Polycomb Repressive Complex 1