Published online: 11 April 2007; | doi:10.1038/news070409-6 /
http://www.nature.com/news/2007/070409/full/070409-6.html
How to stop cancer from spreading
Breast cancer kept from the lungs of mice with simple drug cocktail.Helen Pearson


| Targetting four genes with drugs can stop at least one type of breast cancer from spreading in mice. Getty |
|
Breast
cancer has been prevented from spreading in mice with a simple cocktail
of drugs, some of which are already approved for human use.
The
spread, or metastasis, of cancer is the most dreaded aspect of the
disease: tumours formed this way are responsible for 90% of cancer
deaths. But the process has been difficult to fathom - two tumours may
by all appearances be identical, yet one will spread and one will not.
And a tumour may shed hundreds or thousands of cells into the
bloodstream every day, of which only a tiny fraction will successfully
lodge in a new site and start to proliferate into a new cancer.
In
2005, Joan Massagué at the Memorial Sloan-Kettering Cancer Center in
New York identified a roster of genes that seem to help breast cancer
cells to metastasize to the lung.
Now Massagué's team has shown how four of these genes specifically work
in concert to fuel metastasis. Addressing these four genes with drugs,
they show in mice, has a dramatic effect.
Massagué
hopes that this approach will work better than existing treatments,
because it is targeted against genes now proven to fuel tumour growth
and metastasis. And, he notes, two of the drugs are already in clinical
use, which should speed clinical trials. "You couldn't have it better,"
he says. Other researchers say they would like to see data from human
patients before getting too excited.
Four togetherThe
researchers proved the action of the four genes by silencing them in a
line of human breast cancer cells, before injecting them into mice. The
gene silencing halted the growth of breast tumours in the mice, and
almost completely blocked the formation of lung metastases, they report
in
Nature. Silencing only one of the genes at a time, by contrast, had far less effect.
The team propose that the four genes (called
EREG,
MMP1,
MMP2 and
COX2)
are vital both for aggressive growth of the primary tumour and for
metastasis : they help to hijack a network of blood vessels to nourish
the tumour's own growth, help tumour cells escape into these same blood
vessels to reach the lung, and help them to weasel their way through
the capillary wall, set up shop and grow.
The
researchers showed that a combination of existing drugs known to
inhibit the genes' action - two approved drugs called cetuximab and
celecoxib, plus an experimental one called GM6001 - had a similar
effect to silencing the genes. The two approved drugs on their own also
served to stop the cancer spread.
Massagué
says the next step is to find women whose breast tumours are relying on
these four genes, and to test whether this combination of drugs would
help to protect them from lung cancer. He is now working with doctors
to initiate clinical trials.
Born to killThe
study challenges a long-standing idea that the tendency to metastasize
is picked up late in a tumour's life. Massagué's results support an
alternative hypothesis, that certain tumour cells possess the ability
to metastasize from the outset - and in this case, the same genes that
drive the growth of the primary tumour are the ones that drive the
cells to metastasize.
Researchers don't yet know whether these four genes are
also involved in the metastasis of other cancer types. There are now
thought to be hundreds of different cancer types and it is conceivable
that each uses slightly different ploys for growing and spreading. That
would make it much harder to treat. "I hope there are rules," says
Christoph Klein, who studies metastasis at the University of
Regensburg, Germany.
There
are many other aspects of metastasis that remain mysterious. Some
patients turn up at the doctor with metastases even though,
mysteriously, their primary tumour is never found. And little is known
about why particular cancers show a proclivity for spreading to
particular tissues, such as breast cancer's particular preference to
target bone and lung.
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