Chemotherapy drugs work better against cancer when combined with cycles of short, severe fasting, a study has found.
According to world-science.net, researchers suggest the fasting
might help because normal cells tend to put off trying to divide
when nutrients are lacking—but cancer cells keep trying, and this
process ultimately kills them.
Fasting, even on its own, effectively treated a majority of
cancers tested in mice, including transplanted cancer tumors made
of human cells, researchers said. Their study, published in the
journal Science Translational Medicine, found that five out of
eight cancer types in mice responded to fasting alone: just as with
chemotherapy, fasting slowed the growth and spread of tumors. And
without exception, “the combination of fasting cycles plus
chemotherapy was either more or much more effective than chemo
alone,” said study senior author Valter Longo of the University of
Southern California.
Multiple cycles of fasting combined with chemotherapy cured
20 percent of mice with a highly aggressive type of children’s
cancer that had spread throughout the body, and 40 percent of mice
with a more limited spread of the same cancer, the authors added. No
mice survived in either case if treated only with chemotherapy.
“We don’t know whether in humans it’s effective,” said Longo,
adding that it would take a clinical trial of several years to find
out. Results from the first phase of a clinical trial with breast,
urinary tract and ovarian cancer patients, conducted at the
university, have been submitted for presentation at the next
annual meeting of the American Society of Cancer
Oncologists. But the first phase tests only the safety of a
therapy, in this case whether patients can tolerate two-day fasts
before and after chemotherapy.
Reported by www.world-science.net
Fasting isn’t safe for everyone, Longo warned. The clinical
trial didn’t enroll patients who already had lost more than 10
percent of their normal weight or who had other risk factors, such
as diabetes. Fasting also can cause a drop in blood pressure and
headaches, which could make driving and other activities
dangerous for some.
In a case report study with self-reported data published in the
journal Aging in 2010, 10 cancer patients who tried fasting cycles
perceived fewer side effects from chemotherapy.
In mice, the new study found that fasting cycles without
chemotherapy could slow the growth of breast cancer as well as the
cancers melanoma, glioma and human neuroblastoma. In several
cases, the fasting cycles were as effective as chemotherapy,
the researchers said. Fasting also extended survival in mice
bearing a human ovarian cancer. In the case of melanoma, a
deadly skin cancer, the cancer cells became resistant to fasting
alone after a single round, but the single cycle of fasting was as
effective as chemothera in reducing the spread of cancer to
other organs.
For all cancers tested, fasting combined with chemotherapy
improved survival, slowed tumor growth and/or limited the spread
of tumors, the investigators reported.
As with any potential cancer treatment, fasting has its limits,
Longo stressed. The growth of large tumor masses was reduced by
multiple fasting and chemotherapy cycles, but cancer-free
survival wasn’t achieved, the researchers said. Longo speculated
that cells inside a large tumor may be protected somehow or that
the variety of mutations in a large tumor may make it more
adaptable.
But he noted that in most patients, oncologists have at least one chance to attack the cancer before it grows too large.
Longo and collaborators at the U.S. National Institute on
Aging studied one type of breast cancer in detail to try to
understand fasting’s effects. While normal cells deprived of
nutrients enter a dormant state similar to hibernation, the
researchers saw that the cancer cells tried to make new proteins and
took other steps to keep growing and dividing. The result, Longo
said, was a “cascade of events” that led to the creation of
damaging molecules called free radicals. These broke down the
cancer cells’ DNA and destroyed them.
“The cell is, in fact, committing cellular suicide. What we’re
seeing is that the cancer cell tries to compensate for the lack of
all these things missing in the blood after fasting. It may be
trying to replace them, but it can’t,” Longo said.
The new study bookends research published in the journal
Proceedings of the National Academy of Sciences in 2008. In that
work, Longo’s team showed that fasting protected normal cells
against chemotherapy, but didn’t address the effect on cancer
cells. The study also focused only on a single cancer and
chemotherapy drug. The new work extends those results by showing
that fasting not only fails to protect cancer cells, but makes them
more vulnerable, Longo said. He called the effect “different
stress sensitization” to reflect the change in vulnerability
between normal and cancerous cells.
Longo’s interest in fasting and cancer grew from years of
studies on the beneficial effects of fasting in yeast and other
organisms. He found 15 years ago that starved yeast cells enter a
stress-resistant mode as they wait for better times. By contrast, he
said, the mutations in cancer cells come at a cost, such as a loss
in adaptability to diverse environments.
“A way to beat cancer cells may not be to try to find drugs that
kill them specifically but to confuse them by generating extreme
environments, such as fasting, that only normal cells can quickly
respond to,” Longo said.
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