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Researchers
at the Dana-Farber Cancer Institute have discovered six new genes
linked to inherited breast cancer.
A mutation
of any of the six genes involved in Fanconi anemia (a rare childhood
disease) can increase a woman's risk of developing breast cancer,
according to the study published in the journal Science.
The discovery
of the six genes raises the total of breast cancer susceptibility
genes to eight, including the BRCA1 and BRCA2 mutations.
"Just
as women today can be tested for BRCA1 and BRCA2 mutations to
determine if they have an inherited predisposition for breast
cancer, testing for mutations in these other six genes may soon
become a routine part of gauging inherited breast cancer risk,"
said Dr. Alan D'Andrea, senior author of the study. "Women
and their doctors can then use the information in deciding how
to keep that risk at a minimum."
The discovery
of the new breast cancer susceptibility genes came from more than
10 years of research by D'Andrea into Fanconi anemia, a condition
that affects only 500 families in the United States. Children
with the condition develop bone marrow failure early in life and
are especially susceptible to developing various forms of cancer
if they live into early adulthood.
"This
work is a prime example of how research into rare conditions can
lead to better diagnosis and treatment for people with far more
common diseases," said D'Andrea.
Now that the
association between the six Fanconi genes and breast cancer has
been found, researchers are hopeful they will be able to find
new tests for determining who is at risk for inherited breast
cancer, and develop new drugs targeted at these mutated genes.
Other
sources: Dana-Farber Cancer Institute
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