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PMID: 18565101 Published · ppublish English Journal Article Review

The Notch pathway in prostate development and cancer.

Differentiation; research in biological diversity ·Vol. 76 ·No. 6 ·2008-07-00 ·Pages 699-716

Leong KG, Gao WQ

Abstract

The Notch family of transmembrane receptors are important mediators of cell fate determination. Accordingly, Notch signaling is intimately involved in the development of numerous tissues. Recent findings have highlighted a critical role for Notch signaling in normal prostate development. Notch signaling is required for embryonic and postnatal prostatic growth and development, for proper cell lineage specification within the prostate, as well as for adult prostate maintenance and regeneration following castration and hormone replacement. Evidence for Notch as a regulator of prostate cancer development, progression, and metastasis has also emerged. This review summarizes our current understanding of the role of Notch pathway elements, including members of the Jagged, Delta-like, hairy/enhancer-of-split, and hairy/enhancer-of-split related with YRPW motif families, in prostate development and tumorigenesis. Data supporting Notch pathway elements as oncogenes and tumor suppressors in prostate tumors, as well as data implicating Notch receptors and ligands as potential markers of normal prostate stem/progenitor cells and prostate cancer stem/initiating cells, are also presented.

MeSH Terms
Animals Humans Male Neoplasms/physiopathology Prostate/growth & development,pathology Receptors, Notch/metabolism Signal Transduction Stem Cells/metabolism,pathology
Chemicals
Receptors, Notch
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Leong Kevin G
Department of Molecular Biology, Genentech Inc., 1 DNA Way Southern San Francisco, CA 94080, USA.
Gao Wei-Qiang
Article Info
Journal
Differentiation; research in biological diversity
Abbr.
Differentiation
ISSN
1432-0436
Published
2008-07-00
Epub
2008-00-28
Pages
699-716
Language
English
Region
England
NLM ID
0401650
Subset
IM
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