HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Notch protection against apoptosis in T-ALL cells mediated by GIMAP5.

Abstract
Recent studies have highlighted the role of Notch signalling in the development of T cell acute lymphoblasic leukaemia (T-ALL). Over-expression of Notch3 and gain of function mutations in the Notch1 gene have been reported. The aims of this study were to determine the effect of Notch signalling on apoptosis in human T-ALL cell lines and to identify targets of Notch signalling that may mediate this effect. Functional studies showed that inhibition of Notch signalling using gamma secretase inhibitors promoted glucocorticoid-induced apoptosis in cells carrying gain of function mutations in Notch1. Moreover, ectopic expression of constitutively activated Notch provided protection against glucocorticoid-induced apoptosis, indicating that signalling via Notch may also contribute to the development of T-ALL by conferring resistance to apoptosis. Microarray analysis revealed that GIMAP5, a gene coding for an anti-apoptotic intracellular protein, is upregulated by Notch in T-ALL cell lines. Knockdown of GIMAP5 expression using siRNA promoted glucocorticoid-induced apoptosis in T-ALL cells carrying gain of function mutations in Notch1 and in T-ALL cells engineered to express ectopic constitutively activated Notch indicating that Notch signalling protects T-ALL cells from apoptosis by upregulating the expression of GIMAP5.
AuthorsNicholas Chadwick, Leo Zeef, Virginia Portillo, Joanna Boros, Sarah Hoyle, Jaap C L van Doesburg, Anne-Marie Buckle
JournalBlood cells, molecules & diseases (Blood Cells Mol Dis) Vol. 45 Issue 3 Pg. 201-9 (Oct 15 2010) ISSN: 1096-0961 [Electronic] United States
PMID20817506 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2010 Elsevier Inc. All rights reserved.
Chemical References
  • GIMAP5 protein, human
  • Glucocorticoids
  • NOTCH1 protein, human
  • NOTCH3 protein, human
  • Protease Inhibitors
  • Receptor, Notch1
  • Receptor, Notch3
  • Receptors, Notch
  • GTP-Binding Proteins
Topics
  • Apoptosis
  • GTP-Binding Proteins (biosynthesis, genetics)
  • Gene Expression Profiling
  • Gene Expression Regulation, Leukemic (drug effects, genetics)
  • Gene Knockdown Techniques
  • Glucocorticoids (pharmacology)
  • Humans
  • Jurkat Cells
  • Oligonucleotide Array Sequence Analysis
  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma (genetics, metabolism)
  • Protease Inhibitors (pharmacology)
  • Receptor, Notch1 (genetics, metabolism)
  • Receptor, Notch3
  • Receptors, Notch (genetics, metabolism)
  • Signal Transduction
  • Up-Regulation (drug effects, genetics)

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: