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TI-3D Seed Grants
Fortilin
The
NS1 Protein
Regulation of sGC
function by non-heme tetrapyrrole macrocycles
FastLab
Virtual
Screening
Protein
Kinases
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Postdoctoral Research Initiatives

Fortilin
Stephen Martin, PhD - Department of
Chemistry & Biochemistry, The University of Texas at Austin
Ken Fujise, MD - Institute for Molecular Medicine, The University of
Texas Health Science Center
Fortilin is a 172 amino-acid polypeptide
with potent anti-apoptotic function. In a differential gene
expression analysis between cancer cell lines exhibiting benign and
malignant phenotypes, fortilin showed the strongest differential
expression among 263 genes that were significantly up- or
down-regulated. Fortilin is highly overexpressed in breast,
prostate, lung cancers, and it seems likely that fortilin, by virtue
of its anti-apoptotic activity, allows cancerous cells to be more
aggressive and evade the tumor surveillance system of the host.
These observations suggest that anti-fortilin agents might be
powerful anti-cancer drugs, but no systematic effort to verify this
exciting hypothesis has been undertaken. We have recently developed
a facile and reliable screening method to identify compounds,
especially small molecules, that interact with fortilin, and we have
identified a lead compound. We will now systematically design and
synthesize small molecular weight compounds that are related to the
lead compound or that are identified by virtual screening and
computational docking studies. These new compounds will be rapidly
screened in both in vitro and in vivo systems. The ultimate goal
will be to identify potent fortilin inhibitors that will be powerful
anticancer agents.
Dr. Ken Fujise is Associate Professor of Medicine and of Molecular
Medicine at Brown Foundation Institute of Molecular Medicine for the
Prevention of Human Diseases and Division of Cardiology, within
University of Texas Health Science Center at Houston. He also serve
as a faculty member of Graduate School for Biomedical Sciences. Dr.
Fujise is a practicing physician who pursues basic biomedical
research studying the role of fortilin in atherosclerogenesis and
tumorigenesis. Atherosclerogenesis and tumorigenesis share many
signaling pathways in common. Fortilin was originally discovered in
his laboratory as a novel anti-apoptotic molecule. Fortilin research
in Dr. Fujise' s laboratory has been supported by National
Institutes of Health, American Heart Association, and MacDonald
General Research Fund. Dr. Fujise's laboratory is located in Sarofim
Research Building at Brown Foundation Institute of Molecular
Medicine.
Ken Fugise
Stephen Martin
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