Medical Journals

A Functional Genetic Screen Identifies Tfe3 As a Gene That Confers Resistance to the Anti-proliferative Effects of the Retinoblastoma Protein and Transforming Growth Factor-beta.

Authors:
  • Nijman Sebastian M B
  • Hijmans E Marielle
  • El Messaoudi Selma
  • van Dongen Miranda M W
  • Sardet Claude
  • Bernards RenĂ©

From: Division of Molecular Carcinogenesis and Centre for Biomedical Genetics, The Netherlands Cancer Institute, 121 Plesmanlaan, 1066 CX Amsterdam, The Netherlands.

The Journal of biological chemistry

  • Publish Date: Aug 2006
  • ISSN: 0021-9258
  • Volume: 281
  • Issue: 31
  • Pages: 21582-7
  • Medium: Print
  • Language: English
  • Citation (JAMA): Nijman Sebastian M B, Hijmans E Marielle, El Messaoudi Selma, et al. A Functional Genetic Screen Identifies Tfe3 As a Gene That Confers Resistance to the Anti-proliferative Effects of the Retinoblastoma Protein and Transforming Growth Factor-beta.. J. Biol. Chem. Aug 2006;281:21582-7

Abstract

The helix-loop-helix transcription factor TFE3 has been suggested to play a role in the control of cell growth by acting as a binding partner of transcriptional regulators such as E2F3, SMAD3, and LEF-1. Furthermore, translocations/TFE3 fusions have been directly implicated in tumorigenesis. Surprisingly, however, a direct functional role for TFE3 in the regulation of proliferation has not been reported. By screening retroviral cDNA expression libraries to identify cDNAs that confer resistance to a pRB-induced proliferation arrest, we have found that TFE3 overrides a growth arrest in Rat1 cells induced by pRB and its upstream regulator p16(INK4A). In addition, TFE3 expression blocks the anti-mitogenic effects of TGF-beta in rodent and human cells. We provide data supporting a role for endogenous TFE3 in the direct regulation of CYCLIN E expression in an E2F3-dependent manner. These observations establish TFE3 as a functional regulator of proliferation and offer a potential mechanism for its involvement in cancer.

Mesh Headings (Keywords): Animals, Cell Proliferation, Cells, Cultured, Cyclin E, DNA, Complementary, E2F3 Transcription Factor, Epithelial Cells, Fibroblasts, Gene Expression Regulation, Gene Library, Humans, Mink, Rats, Retinoblastoma Protein, Transfection, Transforming Growth Factor beta


Check for Full Text / PubMed Unique Identifier (PMID): 16737956


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.