TPO-Induced Metabolic Reprogramming Drives Liver Metastasis of Colorectal Cancer CD110+ Tumor-Initiating Cells

Cell Stem Cell. 2015 Jul 2;17(1):47-59. doi: 10.1016/j.stem.2015.05.016.

Abstract

Liver metastasis is a leading cause of death in patients with colorectal cancer. We previously found that colorectal cancer tumor-initiating cells (TICs) expressing CD110, the thrombopoietin (TPO)-binding receptor, mediate liver metastasis. Here, we show that TPO promotes metastasis of CD110+ TICs to the liver by activating lysine degradation. Lysine catabolism generates acetyl-CoA, which is used in p300-dependent LRP6 acetylation. This triggers tyrosine phosphorylation of LRP6, ultimately activating Wnt signaling to promote self-renewal of CD110+ TICs. Lysine catabolism also generates glutamate, which modulates the redox status of CD110+ TICs to promote liver colonization and drug resistance. Mechanistically, TPO-mediated induction of c-myc orchestrates recruitment of chromatin modifiers to regulate metabolic gene expression. Our findings, therefore, establish TPO as a component of the physiological environment critical for metastasis of colorectal cancer to the liver.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyl Coenzyme A / metabolism
  • Acetylation
  • Animals
  • Cell Line, Tumor
  • Cellular Reprogramming
  • Colorectal Neoplasms* / metabolism
  • E1A-Associated p300 Protein / metabolism
  • Fatty Acids / biosynthesis
  • Genes, myc
  • Heterografts
  • Humans
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / secondary*
  • Low Density Lipoprotein Receptor-Related Protein-6 / metabolism
  • Lysine / metabolism
  • Mice
  • Mice, Knockout
  • Neoplastic Stem Cells / metabolism*
  • Oxidative Stress
  • Receptors, Thrombopoietin / metabolism
  • Thrombopoietin / deficiency
  • Thrombopoietin / genetics
  • Thrombopoietin / metabolism*

Substances

  • Fatty Acids
  • LRP6 protein, human
  • Low Density Lipoprotein Receptor-Related Protein-6
  • Receptors, Thrombopoietin
  • MPL protein, human
  • Acetyl Coenzyme A
  • Thrombopoietin
  • E1A-Associated p300 Protein
  • EP300 protein, human
  • Lysine