By ISRAEL21c Staff
August
23, 2010
A gene affecting chronic pain caused by nerve injury
has been identified by Israeli and international researchers, opening the way
for new treatment approaches.
Understanding the genetics of pain: Prof.
Marshall Devor and Prof. Ariel Darvasi of the Hebrew University of Jerusalem.
A gene associated with susceptibility to chronic pain
caused by nerve injury in humans has been identified by a team of Israeli and
international researchers, offering hope of new treatments for sufferers
everywhere.
Chronic pain affects about 20 percent of adults
worldwide, and can range from persistent headaches, to back pain, the pain of
arthritis, and even psychogenic pain, where doctors can't find the cause for a
constant pain.
While it is recognized that some people are more
susceptible than others to chronic pain, no one knows why. Given the same injury
and the same operation, people will suffer variable degrees of pain, even under
nearly identical circumstances.
Now researchers at the Hebrew University of Jerusalem (HUJ), the University of
Toronto in Canada, Sanofi-Aventis in Germany and the Karolinska Institute Center
for Oral Biology in Sweden, believe they may have found the answer in genetics.
"The immediate significance is the mere awareness
that differences in pain perception may have a genetic predisposition,"
says Prof. Ariel Darvasi of the Alexander Silberman Institute of Life Sciences
at the Hebrew University. "Our discovery may provide insights for treating
chronic pain through previously unthought-of mechanisms."
The gene at the heart of your pain perception
In a report published late last week in Genome
Research, Darvasi and colleagues identified a region of
mouse chromosome 15 that likely contained a genetic variant or variants
contributing to pain. However, this region contains many genes, and the
responsible variant remained unknown.
Darvasi and his team, which includes Prof. Marshall
Devor of the Hebrew University, undertook two fine-mapping approaches to narrow
down the chromosomal locus to an interval of 155 genes.
By applying bioinformatics approaches and whole genome
microarray analysis, they were able to confidently identify a single gene,
Cacgn2, as the likely candidate. In mouse experiments, the researchers were able
to confirm that Cacfn2 has a functional role in pain.
To find out whether the human version of the gene also
plays a part in chronic pain, the scientists then analyzed a group of breast
cancer patients who experienced chronic pain more than six months after they had
undergone removal or partial removal of a breast. The researchers found that
genetic variants of Cacng2 were significantly associated with this chronic pain.
While cautioning that this association will need
further analysis, the researchers say that the result suggests that this gene is
an important factor in experiencing pain.
The work was supported by the Israel Science
Foundation, the Hebrew University Center for Research on Pain, the Canada
Research Chair Program and the European Community's 6th Framework Program