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PMID: 16288293 Published · ppublish English Journal Article Review

Akt-regulated pathways in prostate cancer.

Oncogene ·Vol. 24 ·No. 50 ·2005-11-14 ·Pages 7465-74

Majumder PK, Sellers WR

Abstract

Prostate cancer remains a major cause of cancer-related mortality. Genetic clues to the molecular pathways driving the most aggressive forms of prostate cancer have been limited. Genetic inactivation of PTEN through either gene deletion or point mutation is reasonably common in metastatic prostate cancer and the resulting activation of phosphoinostide 3-kinase, AKT and mTOR provides a major therapeutic opportunity in this disease as mTOR inhibitors, HSP90 inhibitors and PI3K inhibitors begin to enter clinical development.

MeSH Terms
Humans Male PTEN Phosphohydrolase/genetics,physiology Phosphatidylinositol 3-Kinases/genetics,metabolism Prostatic Neoplasms/genetics,physiopathology Protein Kinases/genetics,physiology Proto-Oncogene Proteins c-akt/genetics,physiology Signal Transduction TOR Serine-Threonine Kinases
Chemicals
Protein Kinases MTOR protein, human Proto-Oncogene Proteins c-akt TOR Serine-Threonine Kinases PTEN Phosphohydrolase PTEN protein, human
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Majumder Pradip K
Department of Medical Oncology, Dana Farber Cancer Institute, Boston, MA 02115, USA.
Sellers William R
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
2005-11-14
Pages
7465-74
Language
English
Region
England
NLM ID
8711562
Subset
IM
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