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Molecular and Cellular Biology, October 2001, p. 6906-6912, Vol. 21, No. 20
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.20.6906-6912.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
RhoB Is Dispensable for Mouse Development, but It Modifies
Susceptibility to Tumor Formation as Well as Cell Adhesion and
Growth Factor Signaling in Transformed Cells
Ai-Xue
Liu,1
Neena
Rane,1
Jeh-Ping
Liu,2,
and
George C.
Prendergast1,3,*
The Wistar Institute,
Philadelphia,1 and The DuPont
Pharmaceuticals Company, Glenolden Laboratory,
Glenolden,3 Pennsylvania, and Center for
Neurobiology and Behavior, Columbia University, New York, New
York2
Received 20 April 2001/Returned for modification 14 June
2001/Accepted 6 July 2001
RhoB is an endosomal small GTPase that is implicated in the
response to growth factors, genotoxic stress, and farnesyltransferase inhibitors. To gain insight into its physiological functions we examined the consequences of homozygous gene deletion in the mouse. Loss of RhoB did not adversely affect mouse development, fertility, or
wound healing. However, embryo fibroblasts cultured in vitro exhibited
a defect in motility, suggesting that RhoB has a role in this process
that is conditional on cell stress. Neoplastic transformation by
adenovirus E1A and mutant Ras yielded differences in cell attachment
and spreading that were not apparent in primary cells. In addition,
transformed
/
cells displayed altered actin and proliferative
responses to transforming growth factor
. A negative modifier role
in transformation was suggested by the increased susceptibility of
/
mice to 7,12-dimethylbenz[a]anthracene-induced skin carcinogenesis and by the increased efficiency of intraperitoneal tumor formation by
/
cells. Our findings suggest that RhoB is a
negative regulator of integrin and growth factor signals that are
involved in neoplastic transformation and possibly other stress or
disease states.
*
Corresponding author. Mailing address: Glenolden
Laboratory, DuPont Pharmaceuticals Company, 500 S. Ridgeway Ave., Rm.
265, Glenolden, PA 19036. Phone: (610) 237-7847. Fax: (610) 237-7937. E-mail: george.c.prendergast{at}dupontpharma.com.

Present address: Department of Neuroscience, University of Virginia
School of Medicine, Charlottesville,
Va.
Molecular and Cellular Biology, October 2001, p. 6906-6912, Vol. 21, No. 20
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.20.6906-6912.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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