HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Binding of the transcription factor Slug to the L1CAM promoter is essential for transforming growth factor-β1 (TGF-β)-induced L1CAM expression in human pancreatic ductal adenocarcinoma cells.

Abstract
Members of the Slug/Snail family of transcription factors are thought to drive epithelial-mesenchymal-transition (EMT) in preneoplastic epithelial cells, thereby contributing to malignant transformation. One mediator in the EMT of pancreatic ductal adenocarcinoma (PDAC) cells and a potential target gene of Slug is the cellular adhesion molecule L1CAM. Using the human pancreatic ductal epithelial cell line H6c7 and the PDAC cell line Panc1, we could show that along with TGF-β1-induced EMT, L1CAM expression is increased in a Slug- but not Snail-dependent fashion. Two E-box recognition motifs in the L1CAM promoter upstream of the most distal transcriptional start site could be verified by gel shift and supershift assay to interact with Slug. ChIP assays detected an increased interaction of Slug with both recognition motifs of the human L1CAM promoter in TGF-β1-treated H6c7 cells, whereas binding of Snail was downregulated. Moreover, ChIP assays with Panc1 cells confirmed this interaction of Slug with the human L1CAM promoter and further detected an interaction of both recognition sites with RNA-polymerase II in a Slug-dependent fashion. Luciferase reporter gene assays using wild-type or single- and double-mutated variants of the L1CAM promoter confirmed transcriptional activation by Slug involving both recognition motifs. By demonstrating the direct transcriptional control of L1CAM expression through Slug during TGF-β1-induced EMT of PDAC cells, our findings point to a novel mechanism by which Slug contributes quite early to tumorigenesis. Moreover, our study is the first one describing the control of the human L1CAM promoter in tumor cells.
AuthorsClaudia Geismann, Alexander Arlt, Iris Bauer, Marco Pfeifer, Uwe Schirmer, Peter Altevogt, Susanne Sebens Müerköster, Heiner Schäfer
JournalInternational journal of oncology (Int J Oncol) Vol. 38 Issue 1 Pg. 257-66 (Jan 2011) ISSN: 1791-2423 [Electronic] Greece
PMID21109948 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Neural Cell Adhesion Molecule L1
  • SNAI1 protein, human
  • Snail Family Transcription Factors
  • Transcription Factors
  • Transforming Growth Factor beta1
Topics
  • Carcinoma, Pancreatic Ductal (genetics, metabolism, pathology)
  • Cell Line, Tumor
  • Humans
  • Neural Cell Adhesion Molecule L1 (biosynthesis, genetics, metabolism)
  • Pancreatic Neoplasms (genetics, metabolism, pathology)
  • Promoter Regions, Genetic
  • Snail Family Transcription Factors
  • Transcription Factors (biosynthesis, genetics, metabolism)
  • Transfection
  • Transforming Growth Factor beta1 (genetics, metabolism, pharmacology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: