ROLE OF SYNAPTOJANIN 2 IN MALIGNANT TRANSFORMATION
ROLE OF SYNAPTOJANIN 2 IN MALIGNANT TRANSFORMATION
批准号:
6644132
负责人:
MARC H SYMONS
金额:
$30.03万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-06-01 至 2005-05-31
关键词:
actins antisense nucleic acid cell proliferation clathrin complementary DNA endocytosis epidermal growth factor growth factor receptors guanine nucleotide binding protein guanosinetriphosphatases intermolecular interaction neoplasm /cancer invasiveness neoplastic transformation oligonucleotides phosphatidylinositols phosphomonoesterases receptor expression tissue /cell culture yeast two hybrid system
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION: (Adapted from the investigator's abstract) 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.
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依托单位:
海外基金