Development and Cancer: At the Crossroads of Nodal and Notch Signaling

Aggressive tumor cells express a plastic, multipotent phenotype similar to embryonic stem cells. However, the absence of major regulatory checkpoints in these tumor cells allows aberrant activation of embryonic signaling pathways, which seems to contribute to their plastic phenotype. Emerging eviden...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2009-09, Vol.69 (18), p.7131-7134
Hauptverfasser: STRIZZI, Luigi, HARDY, Katharine M, SEFTOR, Elisabeth A, COSTA, Fabricio F, KIRSCHMANN, Dawn A, SEFTOR, Richard E. B, POSTOVIT, Lynne-Marie, HENDRIX, Mary J. C
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container_end_page 7134
container_issue 18
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container_title Cancer research (Chicago, Ill.)
container_volume 69
creator STRIZZI, Luigi
HARDY, Katharine M
SEFTOR, Elisabeth A
COSTA, Fabricio F
KIRSCHMANN, Dawn A
SEFTOR, Richard E. B
POSTOVIT, Lynne-Marie
HENDRIX, Mary J. C
description Aggressive tumor cells express a plastic, multipotent phenotype similar to embryonic stem cells. However, the absence of major regulatory checkpoints in these tumor cells allows aberrant activation of embryonic signaling pathways, which seems to contribute to their plastic phenotype. Emerging evidence showing the molecular cross-talk between two major stem cell signaling pathways Nodal and Notch suggests a promising therapeutic strategy that could target aggressive tumor cells on the basis of their unique plasticity, and provide new insights into the mechanisms underlying the re-emergence of developmental signaling pathways during tumor progression.
doi_str_mv 10.1158/0008-5472.can-09-1199
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source MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals
subjects Animals
Antineoplastic agents
Biological and medical sciences
Humans
Medical sciences
Neoplasms - metabolism
Neoplasms - pathology
Nodal Protein - metabolism
Pharmacology. Drug treatments
Receptors, Notch - metabolism
Signal Transduction
Tumors
title Development and Cancer: At the Crossroads of Nodal and Notch Signaling
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