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Researchers
have discovered a new gene that they believe may be a missing
link that triggers both hereditary and spontaneous forms of breast
cancer.
Women who
inherit faulty BRCA genes are at significantly increased risk
of breast cancer. But the new EMSY gene appears to shut down a
form of fully-functioning BRCA -- increasing risk in other women.
Inheriting
faulty BRCA genes gives women a high risk of breast and ovarian
cancer - but only 5% of breast cancers run in families like this.
Scientists
have been hunting for the genes that cause spontaneous breast
cancers ever since the BRCA genes were identified eight years
ago. Only 5 percent of breast cancers run in women inheriting
faulty BRCA genes.
"Discovering
such an important new gene is very exciting and gives us the piece
in the jigsaw we've been looking for," said lead researchers
Tony Kouzarides.
In their study
which will be reported in the journal Cell, the researchers said
tests on hundreds of tumor samples revealed that 13 percent of
breast cancers contained extra copies of the EMSY gene, but it
was never found in normal tissue.
EMSY seems
to play a particularly important role in aggressive forms of breast
cancer, with women whose tumors had extra copies of the EMSY gene
surviving 6.4 years on average compared with 14 years for those
whose breast cancers had normal amounts of EMSY.
Testing for
EMSY early in breast cancer treatment might thus enable doctors
to predict how aggressive the disease is likely to become, and
how aggressively it needs to be treated, the searchers suggested.
Other
Sources: Cell
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