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GeneBlocs Are Powerful Tools to Study and Delineate Signal Transduction Processes That Regulate Cell Growth and Transformation

Authors :
Ira von Carlowitz
Anke Klippel
Anett Schmiedeknecht
Frank Gebhardt
Klaus Giese
Anny Kretschmer
Frauke Leenders
Maria Sternberger
Leonid Beigelman
Frank Czauderna
Mike Engle
Source :
Antisense and Nucleic Acid Drug Development. 12:131-143
Publication Year :
2002
Publisher :
Mary Ann Liebert Inc, 2002.

Abstract

The study of signal transduction processes using antisense oligonucleotides is often complicated by low intracellular stability of the antisense reagents or by nonspecific effects that cause toxicity. Here, we introduce a new class of antisense molecules, so-called GeneBlocs, which are characterized by improved stability, high target RNA specificity, and low toxicity. GeneBlocs allow for efficient downregulation of mRNA expression at nanomolar concentrations, and they do not interfere with cell proliferation. We demonstrate these beneficial properties using a positive readout system. GeneBloc-mediated inhibition of tumor suppressor PTEN (phosphatase and tension homologue detected on chromosome 10) expression leads to hyperactivation of the phosphatidylinositol (PI) 3-kinase pathway, thereby mimicking the loss of PTEN function and its early consequences observed in mammalian cancer cells. Specifically, cells treated with PTEN GeneBlocs show functional activation of Akt, a downstream effector of PI 3-kinase signaling, and exhibit enhanced proliferation when seeded on a basement membrane matrix. In addition, GeneBlocs targeting the catalytic subunit of PI 3-kinase, p110, specifically inhibit signal transduction of endogenous or recombinant PI 3-kinase. This demonstrates that GeneBlocs are powerful tools to analyze and to modulate signal transduction processes and, therefore, represent alternative reagents for the validation of gene function.

Details

ISSN :
10872906
Volume :
12
Database :
OpenAIRE
Journal :
Antisense and Nucleic Acid Drug Development
Accession number :
edsair.doi.dedup.....03d3f17ef82019940a1dd966ce489c33
Full Text :
https://doi.org/10.1089/108729002760220734