The small GTPase Rac1 is essential for the aberrant growth properties and invasive behavior of transformed cells. The long term goals of our laboratory are to elucidate the signaling pathways that are governed by Rac1 to stimulate cell proliferation and invasion. Rac1 regulates a number of cellular functions that are likely to play a role in malignant transformation. These include the inhibition of receptor-mediated endocytosis and the stimulation of lamellipodia formation. Endocytosis contributes to the down-regulation of growth factor receptors and inhibition of endocytic trafficking has been shown to enhance cell proliferation. Lamellipodia are thought to be important for cell motility. He recently identified the phosphatidylinositol 5'-phosphastase synaptojanin 2 as a novel effector of Rac1. Synaptojanins have been implicated in the regulation of receptor-mediated endocytosis and the organization of the actin cytoskeleton, processes that are known to by modulated by phosphatidylinositol metabolism. The overall objective of this proposal is to examine the hypothesis that synaptojanin 2 functions downstream of Rac1 in the regulation of endocytic trafficking and actin dynamics and that these functions in turn contribute to cell transformation and invasion.
In Aim 1 he will study the molecular mechanisms of the regulation of synaptojanin 2 by Rac1.
In Aim 2 he will examine whether synaptojanin 2 mediates the effects of Rac1 on endocytosis and actin cytoskeleton dynamics. To test these hypothesis, he will use two distinct antisense strategies to inhibit expression of synaptorjanin 2. He will complement this approach, he will stimulate synapotjanin 2 activity in cells using expression of a version of synaptojanin 2 that is Rac-1 independent.
In Aim 3 he will use similar strategies to examine the hypothesis that synaptojanin 2 functions downstream of Rac1 in the regulation of cell proliferation and invasion. These studies will contribute to the understanding of the molecular of cancer. Identifying a role for synaptojanin 2 in the regulation of either cell transformation or invasion would suggest novel avenues for cancer therapy.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA087567-01
Application #
6189413
Study Section
Pathology B Study Section (PTHB)
Program Officer
Gallahan, Daniel L
Project Start
2000-06-01
Project End
2004-05-31
Budget Start
2000-06-01
Budget End
2001-05-31
Support Year
1
Fiscal Year
2000
Total Cost
$342,240
Indirect Cost
Name
Picower Institute for Medical Research
Department
Type
DUNS #
City
Manhasset
State
NY
Country
United States
Zip Code
11030
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Salhia, Bodour; Hwang, Jeong Hyun; Smith, Christian A et al. (2008) Role of myosin II activity and the regulation of myosin light chain phosphorylation in astrocytomas. Cell Motil Cytoskeleton 65:12-24
Chuang, Ya-yu; Valster, Aline; Coniglio, Salvatore J et al. (2007) The atypical Rho family GTPase Wrch-1 regulates focal adhesion formation and cell migration. J Cell Sci 120:1927-34
Tran, Nhan L; McDonough, Wendy S; Savitch, Benjamin A et al. (2006) Increased fibroblast growth factor-inducible 14 expression levels promote glioma cell invasion via Rac1 and nuclear factor-kappaB and correlate with poor patient outcome. Cancer Res 66:9535-42
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Valster, Aline; Tran, Nhan L; Nakada, Mitsutoshi et al. (2005) Cell migration and invasion assays. Methods 37:208-15
Chan, Amanda Y; Coniglio, Salvatore J; Chuang, Ya-yu et al. (2005) Roles of the Rac1 and Rac3 GTPases in human tumor cell invasion. Oncogene 24:7821-9
Chuang, Ya-Yu; Tran, Nhan L; Rusk, Nicole et al. (2004) Role of synaptojanin 2 in glioma cell migration and invasion. Cancer Res 64:8271-5
Schlunck, Gunther; Damke, Hanna; Kiosses, William B et al. (2004) Modulation of Rac localization and function by dynamin. Mol Biol Cell 15:256-67

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