TLE4 promotes colorectal cancer progression through activation of JNK/c-Jun signaling pathway

Oncotarget. 2016 Jan 19;7(3):2878-88. doi: 10.18632/oncotarget.6694.

Abstract

The Groucho transcriptional co-repressor TLE4 protein has been shown to be a tumor suppressor in a subset of acute myeloid leukemia. However, little is known about its role in development and progression of solid tumor. In this study, we found that the expression of TLE4 in colorectal cancer (CRC) tissues was significantly higher than that in their matched adjacent intestine epithelial tissues. In addition, high expression of TLE4 was significantly correlated with advanced Dukes stage, lymph node metastasis and poor prognosis of CRC. Moreover, enforced expression of TLE4 in CRC cell lines significantly enhanced proliferation, invasion and tumor growth. On the contrary, knock down of TLE4 repressed cell proliferation, invasion and tumor growth. Furthermore, our study exhibited that the TLE4 promoted cell proliferation and invasion partially via activation of JNK-c-Jun pathway and subsequently increased cyclinD1 and decreased P27Kip1 expression. In conclusion, these results suggested that TLE4, a potential prognostic biomarker for CRC, plays an important role in the development and progression of human CRC.

Keywords: JNK; TLE4; c-Jun; colorectal cancer; proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers, Tumor / metabolism
  • Caco-2 Cells
  • Cell Line, Tumor
  • Cell Proliferation
  • Colorectal Neoplasms / pathology*
  • Cyclin D1 / biosynthesis
  • Cyclin-Dependent Kinase Inhibitor p27 / biosynthesis
  • Disease Progression
  • Enzyme Activation
  • HCT116 Cells
  • HT29 Cells
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Lymphatic Metastasis / pathology
  • MAP Kinase Signaling System / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Invasiveness / pathology
  • Neoplasm Transplantation
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Prognosis
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Transplantation, Heterologous
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Biomarkers, Tumor
  • CCND1 protein, human
  • CDKN1B protein, human
  • Nuclear Proteins
  • RNA, Small Interfering
  • Repressor Proteins
  • TLE4 protein, human
  • Tumor Suppressor Proteins
  • Cyclin D1
  • Cyclin-Dependent Kinase Inhibitor p27
  • JNK Mitogen-Activated Protein Kinases