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Fish Oil And Cancer - New
Findings
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By Ralph W. Moss, Ph.D.
Swedish scientists recently published an important paper on the positive impact
of omega-3 fatty acids (which are found mainly in fish oil) on a certain
type of childhood cancer called neuroblastoma (Gleissman 2010). These Karolinska
Institute scientists had previously shown that DHA (the most unsaturated
form of fatty acid in fish oil) could cause apoptosis (i.e., programmed
cell death) in cancer cells. They have now extended their work to
experimental animals, showing that fish oil supplementation caused either
stabilization or actual regression of tumors in these animals. As they
state, DHA "is a promising new agent for cancer treatment and
prevention of minimal residual disease" (ibid). Their conclusions, as
I shall show, also have relevance to a broader range of adult cancers.
The paper actually encompasses two parts, one on treatment, the other on prevention. In the prevention half, they
gave DHA as a food supplement to rats before the animals were implanted
with human neuroblastoma cells. (Because they
lack a thymus, the rats in question are unable to reject tissue from a foreign
species.) In the treatment half of the study, athymic
rats that already had established neuroblastomas
were force fed DHA daily and their tumor growth and DHA levels were then
monitored. The authors concluded that "untreated control animals
developed progressive disease, whereas treatment with DHA resulted in
stable disease or partial response." The response depending on the
dose of DHA.
Neuroblastoma is a tumor of the sympathetic
nervous system that occurs in children. In fact, it accounts for 6 to 9
percent of all childhood cancers. It is the most deadly solid tumor of
childhood outside the brain. "Despite intensive treatment modalities,
the cure rate for these patients is less than 50 percent," the authors
report, "and the majority experience relapse
from minimal residual disease." Needless to say, there is an urgent
need for new treatment ideas.
There appears to be a very special relationship between DHA and nerve
tissue. For instance, a deficiency of DHA will lead to delayed neural
development. Compared to normal nerve tissue, neuroblastoma
is "profoundly deficient in DHA," whereas the level of the
competing omega-6 fatty acid arachidonic acid
(AA) is increased. This suggested to the authors that "an imbalance
between omega-3 and omega-6 fatty acids may serve as an adaptation
mechanism in nervous system tumors." Logically, then, one might expect
the addition of DHA to slow or even stop the growth of neuroblastoma.
This is indeed what happened when they gave DHA supplements. The authors
reported: "In the DHA-supplemented group the mean time to tumor take
was significantly delayed compared to the control group" (ibid.). One
rat receiving the DHA-enriched diet did not develop tumors at all. In the
treatment part of the study, the median tumor volume index at the end of
the experiment (day 12) was 3.72 for animals receiving one gram of DHA per
kilogram of body weight, 5.47 for animals receiving half a gram per
kilogram of DHA, and 9.48 in the control animals. The results were
statistically significant. Put another way, a high dose of DHA decreased
normal tumor growth by about two-thirds. As was predicted in the authors’
‘omega-3 deficiency’ theory, the level of DHA in the tumor tissue tripled
in the higher-dose treatment group vs. the controls.
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The finding that DHA supplements cut the amount of tumor formation by
two-thirds in experimental rats was astonishing, but not exactly new. It was
in line with previous findings that a fish oil-enriched diet could inhibit
the formation of various other kinds of tumors, including papillomas
(Akihisa 2004), breast cancer (Manna 2008, Yuri 2003, Noguchi 1997), cancers
of the large and small intestines (Toriyama-Baba
2001) lungs (Toriyama-Baba 2001), colon cancer
(Takahashi 1993, Iigo 1997), sarcoma (Ramos 2004), and
prostate cancer (Kelavkar 2006). Other studies have
shown that omega-3 is strongly associated with a decreased risk of
aggressiveness in prostate (Fradet 2006), kidney (Wolk 2006) and breast cancer (Kim 2009).
But DHA supplementation worked better at preventing the occurrence or
recurrence of tumors than at treating established tumors. "Our study
shows that DHA given as a daily oral supplement displays a moderate capacity
to reduce neuroblastoma growth in the majority of
treated animals," Judith Gleissman and her Karolinska coworkers wrote, "but not in all."
Some animals simply did not incorporate DHA into their tumor tissue, and it
was precisely those animals that did not respond to the treatment.
Do these recent Swedish findings have relevance to cancers in humans,
including, but not limited to, children with neuroblastoma?
I believe they do. The authors point to a study in an Inuit population of
Alaska, which has a DHA intake several-fold higher than typical Caucasians.
In one study, this group’s neuroblastoma rate was
one-tenth that of a comparable lower-48 American population (Dewailly 2001). Alarmingly, in most of America, the ratio
of omega-3 to omega-6 fatty acids has "dropped precipitously" over
the past few decades. This bodes ill for American children and their parents
and loved ones.
Eating more fatty fish seems, even more than ever, a prudent thing to do.
Children, too, should be encouraged to increase their DHA intake through
fatty fish consumption. However, with the Gulf of Mexico oil spill, finding
good sources of non-contaminated fish is likely to become even more difficult
than it already has been. High quality supplements of DHA and EPA may thereore be the best solution for most readers. For
vegetarians, getting sufficient amounts of DHA and EPA can be a challenge.
The best sources are walnuts, flaxseeds and flaxseed oil, olive oil, canola
(rapeseed) oil, and avocado. DHA supplements derived from microalgae, not
fish, are also readily available. There are also three or four clinical trials
underway to test the effect of DHA and other omega-3 fatty acids in various
kinds of cancer, such as lung, breast and lymphoma. Readers can find out
about these by entering the terms "DHA," "EPA" and cancer
into the Clinicaltrials.gov database.
References:
Dewailly E, Blanchet C, Lemieux S, Sauve L, Gingras S, Ayotte P, Holub BJ. n-3 Fatty acids and cardiovascular disease risk factors
among the Inuit of Nunavik. Am J Clin Nutr 2001;74:464-73.
Fradet V, Cheng I, Casey G, Witte JS. Dietary
Omega-3 Fatty Acids, Cyclooxygenase-2 Genetic Variation, and Aggressive
Prostate Cancer Risk. Clin Cancer Res
2009.
Gleissman H, Segerström
L, Hamberg M, Ponthan F, Lindskog M, Johnsen JI, Kogner P. Omega-3 fatty acid supplementation delays the
progression of neuroblastoma in vivo. Int J Cancer. 2010 May 24. [Epub
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Iigo M, Nakagawa T, Ishikawa C, Iwahori Y, Asamoto M, Yazawa K, Araki E, Tsuda H. Inhibitory
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J, Dhir R, Kim P, Allen KG, McHugh K. Prostate
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B, Chatterjee M, Panda A, Srivastava
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Takahashi M, Minamoto T, Yamashita N, Yazawa K, Sugimura T, Esumi H. Reduction
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