Sciellin mediates mesenchymal-to-epithelial transition in colorectal cancer hepatic metastasis

Oncotarget. 2016 May 3;7(18):25742-54. doi: 10.18632/oncotarget.8264.

Abstract

Hepatic metastasis is the major cause of mortality in colorectal cancer (CRC) patients. Using proteomic analysis, we found sciellin (SCEL) to be specifically expressed in hepatic metastatic CRC cell lines. SCEL knockdown increased CRC cell migration and invasion, while overexpression had the opposite effect. SCEL knockdown also caused cancer cells to form more invasive structures within 3D cultures, increased the mesenchymal marker vimentin, and attenuated the epithelial marker E-cadherin. SCEL increased WNT signaling by activating β-catenin and its downstream target c-myc, and activated mesenchymal-to-epithelial transition (MET) through a SCEL-β-catenin-E-cadherin axis. SCEL showed higher expression in late stage primary CRC than in its hepatic metastatic counterpart. SCEL expression is dynamically modulated by TGF-β1 and hypoxia, revealing a plastic MET mechanism for tumor colonization. Intrahepatic injection in immunodeficient mice revealed that SCEL is necessary for metastatic CRC tumor growth in the liver. These results demonstrate that SCEL is a MET inducer dynamically regulated through the metastasis process. They suggest SCEL may be a useful therapeutic target for preventing or eliminating CRC hepatic metastasis.

Keywords: SCEL; colorectal cancer; hepatic metastasis; mesenchymal-to-epithelial transition.

MeSH terms

  • Animals
  • Carrier Proteins / metabolism*
  • Cell Line, Tumor
  • Cell Movement / physiology
  • Cell Transdifferentiation / physiology*
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • Epithelial-Mesenchymal Transition*
  • Heterografts
  • Humans
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / secondary*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Metastasis

Substances

  • Carrier Proteins
  • SCEL protein, human