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Researchers
at the Salk Institute have identified the probable link between
the breast cancer drug Herceptin and cardiac failure, a common
side effect of the treatment.
Herceptin
targets the HER2 protein, which is over abundant in some breast
cancers. New findings show that, in mice, erbB2 (the mouse
version of HER2) is needed for heart cells to function properly.
"It
was possible that Herceptin triggered cardiac malfunction
by a number of mechanisms, but now it appears to be that the
drug's direct action on erbB2 is the culprit," said Kuo-Fen
Lee, associate professor and senior author of the study published
in Nature Medicine.
It should
be possible to develop new generations of drugs that can provide
the benefits of Herceptin while minimizing harmful effects
on heart function, said Lee.
"To
do that we need to know more about the role of erbB2 in both
cancer and heart cells," he added.
Researchers
engineered mice that would stop making erbB2 selectively in
their heart tissue. Hearts from the mice, examined at one
to six months of age, showed clear signs of cardiomyopathy
similar to those seen in Herceptin-related cardiac dysfunction.
"This
mouse model will help us identify new mechanisms to protect
patients from Herceptin cardiomyopathy, and thereby allow
more aggressive and early use of Herceptin for a broad range
of human cancers," said Ken Chien, director of the Institute
of Molecular Medicine at the University of California, San
Diego and co-author of the study.
Because
all women taking Herceptin are also given other anti-cancer
drugs including anthracyclines, and that therapy tends to
increase cardiac dysfunction in patients, researchers also
studied the effects of anthracyclines on the erbB2 mutant
mice.
The loss
of erbB2 function caused by Herceptin makes cardiac muscle
more susceptible to anthracycline toxicity, reported Lee.
"These
results suggest it may be appropriate to examine alternative
chemotherapeutic agents in combination with Herceptin, in
order to avoid the increased risk of heart disease associated
with combined Herceptin/anthracycline therapy," said
Lee.
Researchers
are focusing their efforts on developing agents that can stimulate
the heart, allowing the use of Herceptin aggressively while
protecting the heart.
Source:
Breast Cancer
Week of June 16, 2002

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