X-Message-Number: 17657
From: Brent Thomas <>
Subject: very interesting life extension research
Date: Wed, 26 Sep 2001 09:57:04 -0400

Still kind of fundamental research at this point but very interesting in its
potential

from http://www.sciencedaily.com/releases/2001/09/010925070413.htm

Source:   University Of Illinois At Chicago (http://www.uic.edu/) 
 
 
Date:   Posted 9/25/2001 

University Of Illinois At Chicago Researchers Find "Fountain Of Youth" Gene 

The body's inability to grow new tissue as it ages might be overcome by
increasing the activity of a gene known as FoxM1B, according to a study
published in the Sept. 25 issue of the Proceedings of the National Academy
of Science. 
By increasing the activity, or expression, of this gene in aged experimental
mice, Robert Costa, professor of molecular genetics at the University of
Illinois at Chicago College of Medicine, and his colleagues were able to
restore the regeneration of liver cells to rates of growth typical of young
mice. 

Because in humans the FoxM1B gene exists not only in the liver but also
throughout the body, the researchers believe their discovery might one day
be used in gene therapy in the elderly to restore their ability to replace
old cells with new ones and rejuvenate worn-out organs. Cells divide
normally when stimulated by FoxM1B, making it an ideal candidate for use in
therapeutic intervention, according to Costa. 

"Ponce de Leon was looking in the wrong place for the fountain of youth,"
said Costa. "He should have been looking for the FoxM1B gene." 

According to Costa, earlier studies had shown that age-related defects in
the proliferation of cells found in connective tissue throughout the body
are associated with diminished expression of FoxM1B. Defects in cell
proliferation lead to chromosomal abnormalities and mutations, which in turn
lead to a variety of health problems found in older people, including
infections, organ failure, Alzheimer's disease, dementia and an increased
incidence of cancer. 

In the elderly, cells grow slowly in response to injury and do not
proliferate adequately to replenish damaged cells in the skin, hair, muscle
and other tissues. As a consequence, injuries take longer to heal, and
certain physical changes occur-for example, the skin wrinkles and muscles
atrophy. 

In the present study, aged mice were fitted with a "promoter" to increase
expression of the FoxM1B gene. After undergoing a partial hepatectomy, in
which a portion of the liver was removed, the mice rapidly regenerated new
tissue, unlike typical aged mice. 

The DNA in the regenerating liver cells replicated normally, and cells
divided just as they do in the livers of young mice that have been injured.
Furthermore, laboratory studies showed that increasing expression of the
FoxM1B gene in aged mice restored as well the activity of numerous other
genes involved in cell division. 

"FoxM1B clearly regulates the expression of a whole network of genes that
are required for cells to multiply," said Costa. 

Importantly, Costa added, the study indicated that the FoxM1B gene also
controls exit from mitosis, that is, the completion of cell division.
Without that, cells would be abnormal, failing to divide and retaining too
many copies of DNA - defects commonly seen in cancers. 


Other scientists involved in the study were Xinhe Wang, from UIC, Elizabeth
Quail, a visiting scientist from the University of Western Australia,
Nai-Jung Hung, from UIC, Yongjun Tan, from UIC, and Honggang Ye, formerly
from UIC and now at the University of Chicago. 

The National Institute of Diabetes and Digestive and Kidney Diseases of the
National Institutes of Health supported the research.  



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http://www.sciencedaily.com/releases/2001/09/010925070413.htm
 

 
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