TY - JOUR
T1 - Merlin
T2 - Hanging tumor suppression on the Rac
AU - Sherman, Larry S.
AU - Gutmann, David H.
N1 - Funding Information:
We thank Nancy Ratner for helpful discussions and insightful criticism of this manuscript. We apologize to authors whose work could not be cited owing to space limitations. D.H.G. is supported by NIH NS35848 and NS42520; L.S.S. is supported by NIH NS39550.
PY - 2001/11/1
Y1 - 2001/11/1
N2 - Cancer can result from any number of abnormalities in the control of cell-cycle progression, intracellular signaling and transduction of extracellular cues. Many insights into the crucial events that govern the regulation of cell growth have derived from studies of the gene products mutated in inherited cancer syndromes. Recent work on the neurofibromatosis 2 (NF2) tumor suppressor gene suggests that this negative growth regulator might function by modulating growth factor and extracellular matrix (ECM) signals that trigger Rac1-dependent cytoskeleton-associated processes. In this article, we propose a molecular model for NF2 protein (merlin) function in the light of these and related new findings.
AB - Cancer can result from any number of abnormalities in the control of cell-cycle progression, intracellular signaling and transduction of extracellular cues. Many insights into the crucial events that govern the regulation of cell growth have derived from studies of the gene products mutated in inherited cancer syndromes. Recent work on the neurofibromatosis 2 (NF2) tumor suppressor gene suggests that this negative growth regulator might function by modulating growth factor and extracellular matrix (ECM) signals that trigger Rac1-dependent cytoskeleton-associated processes. In this article, we propose a molecular model for NF2 protein (merlin) function in the light of these and related new findings.
UR - http://www.scopus.com/inward/record.url?scp=0035500494&partnerID=8YFLogxK
U2 - 10.1016/S0962-8924(01)02128-6
DO - 10.1016/S0962-8924(01)02128-6
M3 - Review article
C2 - 11684412
AN - SCOPUS:0035500494
SN - 0962-8924
VL - 11
SP - 442
EP - 444
JO - Trends in Cell Biology
JF - Trends in Cell Biology
IS - 11
ER -