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The PTEN/PI3K/AKT Signalling Pathway in Cancer, Therapeutic Implications

Carnero, Amancio, Blanco-Aparicio, Carmen, Renner, Oliver, Link, Wolfgang, Leal, Juan·2008·Current Cancer Drug Targets

Abstract

PTEN/PI3K/AKT constitutes an important pathway regulating the signaling of multiple biological processes such as apoptosis, metabolism, cell proliferation and cell growth. PTEN is a dual protein/lipid phosphatase which main substrate is the phosphatidyl-inositol,3,4,5 triphosphate (PIP3), the product of PI3K. Increase in PIP3 recruits AKT to the membrane where it is activated by other kinases also dependent on PIP3. Many components of this pathway have been described as causal forces in cancer. PTEN activity is lost by mutations, deletions or promoter methylation silencing at high frequency in many primary and metastatic human cancers. Germ line mutations of PTEN are found in several familial cancer predisposition syndromes. Activating mutations which have been reported for PI3K and AKT, in tumours are able to confer tumourigenic properties in several cellular systems. Additionally, the binding of PI3K to oncogenic ras is essential for the transforming properties of ras. In summary, the data strongly support the view of the PTEN/PI3K/AKT pathway as an important target for drug discovery.

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Metadata

Authors
Carnero, A., Blanco-Aparicio, C., Renner, O., Link, W., & Leal, J.
Venue
Current Cancer Drug Targets
Published
2008-05-01
Volume
8
Issue
3
Pages
187-198
ISSN
1568-0096 (ISSN-L)
OpenAlex
W2102353246
Cited by
887
References
0
FWCI
17.50
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The PTEN/PI3K/AKT Signalling Pathway in Cancer, Therapeutic Implications. https://app.cochat.ai/papers/10.2174/156800908784293659
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Carnero, A., Blanco-Aparicio, C., Renner, O., Link, W., & Leal, J. (2008). The PTEN/PI3K/AKT Signalling Pathway in Cancer, Therapeutic Implications. Current Cancer Drug Targets. https://doi.org/10.2174/156800908784293659

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.