Although several human studies
have shown that Se supplementation has a stronger anti-cancer effect in
men than in women, and cohort studies have generally not found an
association between Se status and risk of breast cancer (Waters et al,
2004), Se is nevertheless conceptually/plausibly protective against
breast cancer, and there is substantial evidence from laboratory and
animal trials. Some of these studies have found a particularly strong
anti-breast cancer effect. For example, when mice bred for breast
cancer susceptibility were supplemented with 2 ppm of sodium selenite in
drinking water for 15 months, the incidence of spontaneous mammary
tumours was just 10%, compared to 82% in control mice (Schrauzer &
Ishmael, 1974).
Human case-control studies
include these findings: women with breast cancer had 20% lower Se
status than their matched healthy controls and controls with non-cancer
chronic diseases (Lopez-Saez et al, 2003). Women with breast cancer had
lower serum Se (mean of 50
µg/l)
than women with fibrocystic disease (72
µg/l)
or healthy women (81 µg/l)
(Krsnjavi & Beker, 1990).
Most animal and laboratory
studies have found selenite to be the most effective Se form against
breast cancer cells; however synthetic organoselenium compounds such as
1,4-phenylenebis (methylene) selenocyanate (p-XSC) has been the most
effective form in the DMBA-rat mammary tumour model. It appears that
several mechanisms are involved: inhibition of adduct formation at the
initiation stage of carcinogenesis; inhibition of cell proliferation;
and induction of apoptosis (El-Bayoumy & Sinha, 2004). In addition,
inhibition of angiogenesis (blood vessel formation) in animal mammary
tumour studies was found for Se in three forms: Se-enriched garlic,
sodium selenite, and Se-methylselenocysteine. Selenite was the most
effective form (Jiang etal, 1999).
The strongest evidence for a Se
anti-breast cancer effect in humans comes from a recent study in Poland
which found a strong effect of Se in reducing DNA damage (a probable
cancer precursor) in women who are genetically at high risk of the
disease (Kowalska et al, 2005). Women who have mutations of the
BRCA1 gene have greatly increased risks of breast and ovarian
cancers. The product of this gene is involved in DNA repair, and DNA
damage is an early risk factor for cancer. Women with the BRCA1
gene mutation (n=55) were supplemented with 275
µg
Se/day as sodium selenite for around two months. Cultured blood
lymphocytes were assessed for DNA damage at baseline and then at
conclusion of the study. As a control, relatives of these women, but
who were not carriers of the aberrant gene, were tested as well. The
mean number of chromosome breaks per cell at baseline was 0.63 for the
BRCA1 mutation women, and 0.39 for the controls. After Se
supplementation, the mean breaks for the BRCA1 women had declined
to 0.40, i.e. normal level (Kowalska et al, 2005). [link to
www.cebp.aacrjournals.org/cgi/content/full/14/5/1302]
Although this was not a large
study, the result was statistically highly significant, and suggests
that Se supplementation could reduce breast cancer risk in women with
the BRCA1 mutation. This may also be the case for other
mutations which confer increased risk of breast cancer, but more
intervention trials such as this are required.
References
El-Bayoumy K, Sinha R 2004. Mechanisms of mammary
cancer chemoprevention by organoselenium compounds. Mutat Res
551(1-2): 181-197.
Jiang C, Jiang W, Ip C, Ganther H, Lu J 2000.
Selenium-induced inhibition of angiogenesis in mammary cancer at
chemopreventive levels of intake. Mol Carcinogenesis 26:
213-225.
Kowalska E, Narod SA, Huzarski T, Zajaczek S,
Huzarska J, Gorski B, Lubinski J 2005. Increased rates of chromosome
breakage in BRCA1 carriers are normalized by oral selenium
supplementation. Cancer Epidemiol Biomarkers Prev 14(5):
1302-1306.
Krsnjavi H, Beker D 1990. Selenium in serum as a
possible parameter for assessment of breast disease. Breast Cancer
Res Treat 16: 57-61.
Lopez-Saez JB, Senra-Varela A, Pousa-Estevez L 2003.
Selenium in breast cancer. Oncology 64(3): 227-231.
Schrauzer GN, Ishmael D 1074. Effects of selenium and
of arsenic on the genesis of spontaneous mammary tumors in inbred C3H
mice. Ann Clin Lab Sci 4(6): 441-447.
Waters DJ, Chiang, Cooley DM, Morris JS 2004. Making
sense of sex and supplements: differences in the anticarcinogenic
effects of selenium in men and women. Mut Res 551(1-2):
91-107.
Nutritional supplementation
protocol for prevention & control of breast cancer
All of the components of this
program are backed by solid evidence, and are best taken in combination,
as a number of them are synergistic, i.e. they enhance each other’s
effects. For patients undergoing chemotherapy/radiotherapy, higher
doses of some components (Se, vit E, vit C, green tea, soy, resveratrol)
are recommended. Studies show that certain nutritional/herbal
supplements have the dual effect of reducing the side-effects of
chemotherapy and enhancing its
anti-cancer effect. NB: For women with breast cancer, this protocol
is recommended in addition to standard treatment recommended by your
doctors, not as a substitute.
Selenium. Recommended dose
200 micrograms/day. Sodium selenite is the Se form with most
evidence for anti-breast cancer effect.
Green tea polyphenols.
Strong evidence against breast cancer in animal trials and human
epidemiological studies. Synergistic with
selenium and soy polyphenols.
Soy (or Red clover)
polyphenols (especially genistein) 50 mg/d (e.g. Blackmore’s
Phytolife Plus, around 3 tablets/d).
Omega-3 fatty acids, e.g.
fish oil capsules, 1000 mg/d.
Vitamin C. In the form of
calcium (or sodium) ascorbate, which is non-acidic. One heaped
teaspoon is around 5 grams. Take 5g/day, possibly split into two
doses (as too much at once can cause diarrhoea!), and at a different
time to the selenite, as it can reduce uptake of selenite. Vitamin
C, despite what many doctors and nutritionists say, is useful
against a range of serious conditions, but only at multi-gram
doses. Also synergistic with vit E.
Tomato paste (for the red
carotenoid, Lycopene). Take one heaped dessertspoon/day. NB Lycopene
is much more bioavailable from processed tomato products than from
fresh tomato.
Coenzyme Q10, available in
capsules, for mitochondrial support. Suggest 50-100 mg/day. One
study reported spectacular success in arresting advanced breast
cancer, using 350 mg/day for 12 months. Can be expensive: the best
value is on the Internet.
Grape seed extract (for
Resveratrol). This is a much more concentrated form than occurs in
red wine!
Low-dose aspirin (around
1/3 Disprin/day, or the low-dose coated form, “Cartia”).
Alternatively, include plenty of thyme (high salicylate
concentration) in your diet.
B-vitamins, especially
folate. Take at around double the recommended dose. A VG product is
“Super B50” from Australian Naturalcare Products in Sydney, who
would also have several other items on this list (vitamin E,
magnesium). Ph. 1800 505 355.
Blackcurrant seed oil or
Evening primrose oil (for gamma-linolenic acid).
Regular exercise: 30-45
minutes of vigorous exercise per day (eg tennis, running, fast
walking, exercise bike). Try to get heart rate up to the range of
130-150 beats per minute, but build up gradually to this. Some
light weightlifting is also recommended, not only to improve muscle
strength but also to ward off osteoporosis.
Good, varied diet,
including: cooking with olive oil, drinking soy milk and eating
broccoli, beetroot (including the skin, the best part), carrots,
onions, garlic, apples, berries, nuts, fish, whole grains. Also,
dark chocolate is excellent! Limit your intake of red meat and
dairy products. Can drink a glass or two of wine (preferably red)
or beer a day.
As you’re probably feeling
overloaded by now, the following are optional:
Watercress extract (for
phenethyl isothiocyanate)
Phytic acid (myo-inositol
hexaphosphate, also known as IP6)
Whey protein (for glutathione
precursors)
Pomegranate extract
Isatis extract ( a herb with immune-enhancing and anti-COX 2
and anti-lipoxygenase properties)
European mistletoe extract (Viscum
album)
Linseed/flaxseed
In addition, for
menopausal/post-menopausal women:
Preparations that contain Black
Cohosh and Soy (or Red clover) polyphenols.
DHEA (dehydroepiandrosterone), a
steroid hormone precursor (harmless), that decreases with age. Try the
Internet.
There is no need to take
prescribed hormone replacement therapy (which can have detrimental
side-effects) if these natural supplements are used together with the
diet and exercise regime noted above. Moreover, if you are eating a
varied diet which includes leafy vegetables, whole grains, nuts, etc,
not smoking or drinking to excess, and exercising, you should not
(contrary to popular opinion and much professional advice) require
supplementary calcium. Better to take magnesium, around 350 mg/d.
Strathalbyn, South Australia
Bridgewater on Loddon, Victoria
2 Callington Rd Strathalbyn SA 5255
PO Box 200 Strathalbyn SA 5255
E-mail:
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