CUTL1: a key mediator of TGFbeta-induced tumor invasion

Cell Cycle. 2006 Jan;5(2):132-4. doi: 10.4161/cc.5.2.2311. Epub 2006 Jan 16.

Abstract

The TGFbeta pathway plays a dual role in human carcinogenesis. On one hand, TGFbeta is well known for its ability to inhibit epithelial cell proliferation and promote apoptosis. However, many advanced cancers acquire resistance to the growth-inhibitory effects of TGFbeta and respond to it instead with promotion of proliferation, invasion and tumor progression. The homeobox transcription factor CUTL1, also known as CCAAT displacement protein, CDP or Cux-1, is involved in the control of normal embryonic development and differentiation. Recently, we found that CUTL1 is a transcriptional target of TGFbeta and is an important mediator of the TGFbeta-induced cell migration and invasion. In addition, CUTL1 is highly expressed in various epithelial cancers and seems to negatively correlate with tumor differentiation and patient survival. Therefore we postulate that CUTL1 might be a key mediator of the tumor-promoting effects of TGFbeta in advanced cancers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gene Expression Regulation, Neoplastic
  • Homeodomain Proteins / metabolism*
  • Humans
  • Neoplasm Invasiveness / pathology*
  • Neoplasms / metabolism*
  • Neoplasms / pathology*
  • Nuclear Proteins / metabolism*
  • Repressor Proteins / metabolism*
  • Transcription Factors
  • Transforming Growth Factor beta / metabolism*

Substances

  • CUX1 protein, human
  • Homeodomain Proteins
  • Nuclear Proteins
  • Repressor Proteins
  • Transcription Factors
  • Transforming Growth Factor beta