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PMID: 16848722 Published · ppublish English Journal Article Review

NOTCH signaling as a novel cancer therapeutic target.

Current cancer drug targets ·Vol. 6 ·No. 4 ·2006-06-00 ·Pages 313-23

Miele L, Miao H, Nickoloff BJ

Abstract

NOTCH-ligand interaction is a highly conserved mechanism that regulates specific cell fate decision during development. In addition to its functions in developmental and cell maturation processes, studies indicate that NOTCH activation plays a role in the onset and progression of many human malignancies. The prevailing new strategy for rationally targeted cancer treatment is aimed at the development of target-selective "smart" drugs on the basis of characterized mechanisms of action. The connection between NOTCH signaling and tumorigenesis suggests that NOTCH may be such a target candidate. Gamma-secretase is a large membrane-integral multisubunit protease complex, which is essential for NOTCH receptor activation. Inhibitors of this enzyme are being developed for Alzheimer's disease, due to its role in cleaving beta-amyloid precursor in the brain. Recently, Gamma-secretase inhibitors (GSIs), as well as various biopharmaceutical or genetic NOTCH signaling inhibitors have been suggested as potential novel cancer therapeutic strategies. This review summarizes the evidence linking NOTCH signaling to several types of cancer, as well as the possible therapeutic indications of NOTCH inhibitors and the challenges facing their clinical development.

MeSH Terms
Amyloid Precursor Protein Secretases Animals Antineoplastic Agents/pharmacology,therapeutic use Aspartic Acid Endopeptidases Cell Transformation, Neoplastic Endopeptidases/metabolism Humans Hyaluronan Receptors/metabolism Neoplasms/drug therapy,genetics,metabolism Neoplastic Stem Cells/immunology,metabolism Oligonucleotides, Antisense/genetics,metabolism Protease Inhibitors/pharmacology,therapeutic use RNA Interference RNA, Small Interfering/genetics,metabolism Receptor Cross-Talk Receptors, Notch/antagonists & inhibitors,genetics,metabolism Signal Transduction/drug effects
Chemicals
Antineoplastic Agents Hyaluronan Receptors Oligonucleotides, Antisense Protease Inhibitors RNA, Small Interfering Receptors, Notch Amyloid Precursor Protein Secretases Endopeptidases Aspartic Acid Endopeptidases BACE1 protein, human
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Miele L
Cutaneous Oncology Program, Cardinal Bernardin Cancer Center and Departments of Pathology and Microbiology-Immunology, Loyola University Chicago, Maywood, IL 60153, USA.
Miao H
Nickoloff B J
Article Info
Journal
Current cancer drug targets
Abbr.
Curr Cancer Drug Targets
ISSN
1568-0096
Published
2006-06-00
Pages
313-23
Language
English
Region
Netherlands
NLM ID
101094211
Subset
IM
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