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A simple blood
test for an unusual genetic change may identify people at risk
of colorectal cancer, according to Johns Hopkins University researchers.
While the
blood test does not detect colorectal cancer, it appears to identify
people with a tendency to develop the disease who would benefit
from an early screening test.
Researchers
said this test thus might ultimately reduce the need for everyone
over 50 to have colonoscopies, an uncomfortable colon and rectal
exam can detect precancerous growths before they become life threatening.
The DNA-based
blood test looks for a change called "loss of imprinting"
in the gene for a protein called insulin-like growth factor II
(IGF2). "Loss of imprinting" means that an extra copy
of a particular gene that promotes cell growth is turned on.
"When
you have loss of imprinting of the IGF2 gene in colon cancer,
the mother's gene copy gets turned on by mistake and the cell
gets a double dose of abnormal cell growth," said Johns Hopkins
reneticist Andrew Feinberg.
Feinberg and
his colleagues used the blood test to look for the alteration
in 172 people who were undergoing screening colonoscopies.
They reported
in the journal Science that people with a family history of the
colorectal cancer were about five times more likely to have lost
imprinting in the IGF2 gene, people with a history of precancerous
colorectal growths called adenomas were three times more likely
to have loss of imprinting.
They also
found that loss of imprinting was almost 22 times more common
in patients with a personal history of colorectal cancer were
nearly 22 times more likely to have these markers.
Feinberg emphasised
that the present test is only useful for research purposes, and
said "more efficient tests will take several more years to
develop."
Other
sources: Science
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