Message #39 From:
NewsBot Date: January 17, 2007 04:30:00 AM
GERN News Studies Show Geron's Stem Cell Therapeutic for Spinal Cord Injury Produces Nerve Growth Factors
MENLO PARK, Calif.--(BUSINESS WIRE)--Geron Corporation (Nasdaq: GERN) today reported that studies show
GRNOPC1, the company’s human embryonic stem
cell (hESC)-based oligodendroglial progenitor therapeutic, produces
multiple nerve growth factors, proteins that stimulate the survival and
regeneration of neurons damaged during spinal cord injury.
Published in Stem Cells and Development (Vol. 15, Issue 6,
943-952), the studies conducted by Geron scientists describe a
newly discovered neurotrophic effect that, in addition to the previously
documented in vivo remyelinating activity of these cells (Journal
of Neuroscience, 25 (19): 4694-4705, 2005), serves as a second
mechanism of action that demonstrates the product’s
beneficial effects when injected into animal models of acute spinal cord
injury.
“The work extends our knowledge of the
multiple biological activities of GRNOPC1,”
stated Thomas B. Okarma, Ph.D., M.D., Geron’s
president and chief executive officer. “In
addition to the remyelinating activity as previously reported, GRNOPC1
produces growth factors that can improve the survival and extension of
neuronal circuitry in the spinal cord. The multiple functions of GRNOPC1
affirm the potential therapeutic utility of our cell-based approach to
the repair of spinal cord injury and provide multiple mechanisms within
a single therapy to achieve functional recovery.”
In the published studies, GRNOPC1 was found to produce numerous
neurotrophic factors, including transforming growth factor β1
(TGF-β1), transforming growth factor β2
(TGF-β2), activin A, midkine, vascular
endothelial growth factor (VEGF) and hepatocyte growth factor (HGF).
These factors were all produced at physiologically active levels, and
each has been reported to have trophic effects on neurons associated
with the spinal cord.
In spinal cord injury, neuronal cell loss can occur not only as a result
of the physical trauma of the injury itself, but also due to the
oxidative and inflammatory reaction that subsequently occurs. The
introduction of neurotrophic factors into the lesion site could increase
neuronal survival, decrease dieback of neuronal axons and induce
sprouting of new axons to allow formation of alternative circuitry.
The studies also demonstrate that neurotrophic factors produced by
GRNOPC1 are biologically active. When culture medium used to grow
GRNOPC1 was applied to adult rat sensory neurons, sprouts called “neurites”
emerged from the rat neurons. Media that had not been exposed to GRNOPC1
stimulated significantly less neurite outgrowth.
“Our studies show that multiple neurotrophic
factors are produced by GRNOPC1 that lead to neurite outgrowth,”
said R. Scott Thies, Ph.D., Geron’s lead
investigator on the work. “Depletion or
inactivation of any single factor did not eliminate the neurotrophic
activity exhibited by these cells.”
Geron is developing first-in-class biopharmaceuticals for the treatment
of cancer and degenerative diseases, including spinal cord injury, heart
failure, diabetes and HIV/AIDS. The company is advancing an anticancer
drug and a cancer vaccine that target the enzyme telomerase through
multiple clinical trials. Geron is also the world leader in the
development of human embryonic stem cell-based therapeutics, with its
spinal cord injury treatment poised to be the first product to enter
clinical development. For more information, visit www.geron.com.
This news release may contain forward-looking statements made pursuant
to the “safe harbor”
provisions of the Private Securities Litigation Reform Act of 1995.
Investors are cautioned that such forward-looking statements in this
press release regarding potential applications of Geron’s
human embryonic stem cell technology constitute forward-looking
statements that involve risks and uncertainties, including, without
limitation, risks inherent in the development and commercialization of
potential products, uncertainty of clinical trial results or regulatory
approvals or clearances, need for future capital, dependence upon
collaborators and maintenance of our intellectual property rights.
Actual results may differ materially from the results anticipated in
these forward-looking statements. Additional information on potential
factors that could affect our results and other risks and uncertainties
are detailed from time to time in Geron’s
periodic reports, including the quarterly report on Form 10-Q for the
quarter ended September 30, 2006.