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Cancer Monthly News and CancerWire
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Greetings!
In this edition of
CancerWire we focus on three recent
studies:
New research from UCLA has revealed that natural
chemicals in fruits and vegetables, as well as in wine
and tea, may protect smokers lung cancer.
A study suggests that an extract from a Chinese
medicinal herb attacks breast cancer cells but spares
healthy ones.
A recent study published in the International Journal of
Medical Sciences reports that a combination of
vitamins C and K may help patients with prostate
cancer.
And finally, we report on the recent brain cancer
diagnosis of Senator Edward Kennedy and discuss
the lack of progress in treating this cancer over the
last 30 years.
Disclaimer - Please Read: None of
the information in CancerWire is a
substitute for professional medical advice,
examination, diagnosis or treatment and you
should always seek the advice of your
physician or other qualified health
professional before starting any new
treatment or making any changes to an
existing treatment. No information contained
in Cancer Monthly or CancerWire including the
information below, should be used to
diagnose, treat, cure or prevent any disease
without the supervision of a medical
doctor.
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Lung Cancer and Natural Substances
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Components in Vegetables, Wine, and Tea Might Reduce Smokers' Lung Cancer Risk
By now, it's obvious that smoking can lead to disease,
and that eating a diet rich in fruits and vegetables can
protect against disease. Now researchers have
discovered that natural chemicals in fruits and
vegetables, as well as in wine and tea, might protect
smokers against one disease in particular-lung
cancer.
A team of researchers in California investigated the
effects of natural plant components called flavonoids
in 558 people with lung cancer and 837 people
without lung cancer. Researchers interviewed the
participants about their history of smoking, diet, and
other cancer risk factors and compared these factors
between lung cancer cases and healthy controls.
Smokers who had high levels of certain flavonoids
had a lower risk of developing lung cancer, the
researchers reported in the journal, Cancer. This is a
particularly significant finding, considering that
smoking is implicated in up to 90 percent of lung
cancer cases, according to Zuo-Feng Zhang, MD,
PhD, Professor of Epidemiology at the UCLA School
of Public Health and Jonsson Comprehensive Cancer
Center.
Smokers who ate three servings of vegetables, drank
tea, and had a glass of wine each day had a lower risk
of lung cancer than those who didn't incorporate these
components into their diets. Among the flavonoids that
appeared to be most beneficial were catechin (found
in green tea, black tea, red wine, strawberries),
quercetin (found in apples, onions, beans), and
kaempferol (found in red wine, apples, Brussels
sprouts).
Flavonoids appear to protect against lung cancer in
several ways: they prevent cancer cells from
multiplying, trigger a process of programmed cancer
cell death (apoptosis), block the formation of blood
vessels that feed tumors, and inhibit the action of
highly unstable oxidative molecules in the body called
free radicals, among other functions.
The reason flavonoids affected lung cancer
development in smokers but not in non-smokers
might be that their antioxidant properties work
specifically on the type of damaging molecules
created by tobacco smoking. "Smoking results in
increased oxidative stress and DNA damage, leading
to lung cancer, and flavonoids' antioxidant function
may reduce the damage from tobacco smoking,"
according to Dr. Zhang.
Why certain flavonoids are more protective against
lung cancer development than others is still
unknown. "Our results will encourage laboratory
scientists to work on cell lines and animal models to
find out why some flavonoids can, and some can't
protect against cancer development among smokers,"
Dr. Zhang says. His team will also investigate which
types of vegetables, and how many servings might
offer the greatest protection against lung cancer.
Because this is the first study to document the effects
of flavonoids on lung cancer, more research is
needed before any real health recommendations can
be made. However, it's very clear from this and past
research that quitting smoking, avoiding passive
smoking, and eating a diet rich in fruits and
vegetables may be a good way to protect against lung
cancer, as well as other diseases.
Source:
Cui Y, Morgenstern H, Greenland S, Tashkin DP, Mao
JT, Cai L, Cozen W, Mack TM, Lu QY, Zhang ZF.
Dietary flavonoid intake and lung cancer - a
population-based case-control study. Cancer.
Published online March 7, 2008.
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Breast Cancer and Chinese Herb
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Chinese Herb Attacks Breast Cancer Cells but Spares Healthy Cells
The challenge in treating cancer has
been to selectively target cancer cells without harming
normal cells. Researchers have found a new drug that
appears to do just that-they have discovered that an
herbal drug called BZL101 significantly damages
cancer cells while sparing healthy cells, and now they
think they know how it works.
BZL 101 is an extract from the Chinese medicinal
herb, Scutellaria barbata. (Flower of plant is shown at
left.) In a phase 1 trial, the drug showed promise in
treating advanced breast cancer, but researchers
wanted to find out exactly how the drug kills cancer
cells, and why it spares healthy cells. "I think it's very
important to know the mechanism of action, because
it's difficult to give patients drugs when you have no
idea how they work," explains lead author Emma
Shtivelman, PhD, Director of Cancer Research at
BioNovo, Inc in Emeryville, California. "If you know the
mechanisms you can target the drug more precisely
and predict potential side effects, which are clear
goals of research and development."
Many cancer therapies that kill cancer cells do so by a
process of programmed cell death, called apoptosis.
But this didn't seem to be the case with BZL101,
which had the researchers wondering as to the real
mechanism.
"The buzzword in cancer research for years was
apoptosis-and we saw that BZL101 induces a lot of
cell death, but we couldn't describe it as apoptopic
cell death," says Dr. Shtivelman. In a culture of breast
cancer cells, only 10 to 15 percent of the cancer cells
were killed by apoptosis. For the remainder, there was
obviously a different cause at work.
What the researchers found after treating cancer cell
lines with BZL101 was that the drug triggers high
levels of reactive oxygen species (ROS)-highly
unstable molecules that can damage DNA. "Normal
cells are well equipped to cope with highly reactive
oxygen species because they're harmful," according
to Dr. Shtivelman. Tumor cells, though, already have
high levels of ROS, and the additional ROS induced by
BZL101, "takes them overboard and they die," she
says. Also, because the drug inhibits glycolysis-the
method cancer cells use to produce energy-it can
force them to deplete their energy stores and
essentially starve to death, Dr. Shtivelman and her
colleagues reported in Cancer Biology & Therapy.
Because it spares healthy cells, BZL101 appears to
be very safe overall. The only side effects noted so far
have been mild, including constipation, nausea, and
diarrhea.
The next phase of the research, which will look at the
drug's effectiveness, is slated to be completed in
September 2009. If the results are favorable, the
researchers will move on to phase 3 trials with larger
groups of patients.
The study authors believe BZL offers great promise
over many current cancer therapies because of its low
toxicity and limited risk of side effects. "Conventional
chemotherapeutic drugs hit all proliferating cells in the
body," says Dr. Shtivelman. "That's why cancer
patients who are on chemotherapy lose their hair,
have intestinal problems, and are frequently anemic. If
that can be avoided you can increase the dose, if
necessary. And with BZL101 that seems to be the
case-tumor cells are ready to die when they see the
drug and normal cells remain healthy."
Source:
Fong S, Shoemaker M, Cadaoas J, Lo A, Liao W,
Tagliaferri M, Cohen I, Shtivelman E. Molecular
mechanisms underlying selective cytotoxic activity of
BZL101, an extract of Scutellaria barbata, towards
breast cancer cells. Cancer Biology & Therapy.
2008;7:7(4).
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Prostate Cancer and Vitamins C & K
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Vitamin Combo Slows Prostate Cancer Progression
A treatment combining high doses of vitamins C and
K helps slow the progress of prostate cancer in men
who have not responded to surgery, radiation, and
other standard therapies, according to a recent study
in the International Journal of Medical Sciences.
prostate cancer is the most common cancer in men,
with more than 180,000 new cases diagnosed each
year in the U.S., according to the American Cancer
Society. In men whose cancer is advanced, treatment
usually involves hormone therapy to lower the amount
of male hormones (androgens), which fuel prostate
cancer growth. However, this treatment can have side
effects and it doesn't always work, particularly in men
with a form of prostate cancer that doesn't rely on
male hormones to grow.
In their search for new prostate cancer treatment
options, researchers investigated a therapy called
Apatone, which combines 500 milligrams (mg) of
vitamin C and 5 mg of vitamin K3. Vitamin C acts as
an antioxidant to protect cells against oxidative
damage caused by unstable molecules called free
radicals. Meanwhile, vitamin K3 produces oxidative
stress in the cancer cells, which kills them off via
various mechanisms, says lead author Basir Tareen,
MD, assistant professor of Urologic Oncology at the
Albert Einstein College of Medicine in New York.
The study included 17 prostate cancer patients
(average age, 71) who had failed standard treatments
(surgery, radiation, and hormone therapy). All of the
patients took 10 capsules of Apatone each day for 12
weeks.
Thirteen of the 17 patients showed a real response to
the treatment based on their levels of prostate specific
antigen (PSA)-a marker of prostate cancer
progression. The majority of participants' PSA velocity
(a measurement of how quickly PSA levels rise over
time) decreased, while their PSA doubling time (the
length of time it takes the PSA level to double)
increased, indicating that cancer progression had
slowed.
Most of the patients opted to continue treatment with
Apatone after the study. Many of them said they
felt "better" and more "energetic." Their PSA levels
remained stable, while those who stopped taking
Apatone experienced a spike in PSA levels.
Apatone appeared to be safe and well tolerated, with
no major side effects reported. The only problem
participants experienced was mild gastroesophageal
reflux, which was relieved by taking Apatone with
meals or antacids. Hormone therapy, by comparison,
can lead to side effects such as hot flashes and
weakened bones (osteoporosis), while chemotherapy
can trigger nausea, vomiting, and hair loss. "Certainly
Apatone is better tolerated than androgen deprivation
or chemotherapy in terms of quality of life and side
effects from what we have observed," according to Dr.
Tareen.
Despite the promising results, however, the study
didn't investigate whether treatment with Apatone
actually prolonged patients' survival. "In order to truly
show a survival benefit, we would have to have a
control group of patients who did not receive Apatone,"
Dr. Tareen explains. "For ethical and logistical
reasons, those types of placebo studies are very
difficult to perform and justify."
Further research will help clarify the role of Apatone in
prostate cancer treatment. "Obviously more studies
need to be done in this very challenging patient
population," Dr. Tareen says. An upcoming study will
investigate the use of Apatone in men who are on
long-term hormone therapy for prostate cancer.
Researchers are also looking at whether Apatone
might be useful for other types of cancers, particularly
lung and skin cancers. So far the treatment appears
promising.
If you are interested in learning more about vitamin
therapy, be sure to speak with your licensed
healthcare practitioner.
Sources:
Tareen B, Summers JL, Jamison JM, Neal DR,
McGuire K, Gerson L, Diokno A. A 12 week, open
label, phase I/IIa study using Apatone for the treatment
of prostate cancer patients who have failed standard
therapy. Int J Med Sci. 2008;5:62-67.
American Cancer Society. How many men get prostate cancer?
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Senator Kennedy Diagnosed with Brain Cancer
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Glioblastoma - no significant improvement in survival in 30 years
Senator Edward M. Kennedy, 76, the longtime
Massachusetts Democrat has been diagnosed with a
malignant brain tumor. Preliminary results from the
biopsy revealed a malignant glioma. The most
common type of malignant glioma is called
glioblastoma multiforme or "GBM."
As reported in the New York Times published on May
21, 2008, Kennedy's doctors have stated that "the
usual course of treatment includes combinations of
various forms of radiation and chemotherapy" and
that "decisions regarding the best course of treatment
for Senator Kennedy will be determined after further
testing and analysis."
According to published medical information, survival
for patients with GBM is typically about 12 months.
Our prayers go out to Mr. Kennedy and his family.
Perhaps this unfortunate diagnosis may initiate a
more global discussion on the continued lack of
progress in treating malignant brain cancers.
No Progress in 30 Years
Despite the occasional pronouncements
of "breakthroughs" the improvement in survival for
GBM is practically zero over the last 30 years.
According to The Central Brain Tumor Registry of the
United States, the two year Relative Survival Rate for
GBM from 1973-1994 was 8.8%. It was 8.7% for the
period 1973-2002. The five year Relative Survival Rate
for GBM from 1973-1994 was 3.4%. It was 3.3% for
the period 1973-2002. And the ten year rate for GBM
from 1973-1994 and 1973-2002 was 2.3%. After
nearly 30 years there has been essentially no
improvement in survival despite the millions of dollars
spent on research and treatment.
Targeted Therapies - "Disappointing"
In the last several years there has been research in
the area of targeted therapies like vascular endothelial
growth factor (VEGF). VEGF is an important signaling
protein involved in the growth of blood vessels. A
theory called "anti-angiogenesis" is based on the
concept that it may be possible to starve a tumor by
stopping the growth of new blood vessels that feed
the cancer. While the theory is promising, in clinical
practice with malignant gliomas the results to date
have been disappointing. According to a report
published in March of this year in the journal Expert
Opinion on Emerging Drugs, "Experience with
targeted therapeutics for malignant glioma has been
to date disappointing. These agents are generally well
tolerated, but activity is limited."
Unconventional Thinking - Poly MVA and
Antineoplastons
Has there been any progress whatsoever in treating
GBM and other malignant gliomas? There has been
some intriguing results, but they have not come from
leading medical centers or drug companies.
Poly MVA
Poly MVA was invented by Dr. Merrill Garnett, a
biochemist. It is a dietary supplement based on the
nontoxic chemotherapeutic lipoic acid-palladium
complex (LAPd). LAPd is a liquid crystal that works in
cancer cells by transferring excess electrons from
membrane fatty acids to DNA via the mitochondria. It
has been used as a dietary supplement by thousands
of cancer patients. According to anecdotal reports
published on websites some patients who have
survived glioblastoma and other malignant brain
tumors believe their use of this dietary supplement
may have been partly responsible. Are mainstream
oncologists intrigued by these results? No. Nearly all
conventional oncologists reject this dietary
supplement as a potential therapeutic modality.
Dr. Burzynski's Antineplastons
According to a National Cancer Institute Factsheet:
"Antineoplastons are a group of synthetic compounds
that were originally isolated from human blood and
urine by Stanislaw Burzynski, M.D., Ph.D., in Houston,
Texas. Dr. Burzynski has used antineoplastons to
treat patients with a variety of cancers. In 1991, the
National Cancer Institute (NCI) conducted a review to
evaluate the clinical responses in a group of patients
treated with antineoplastons at the Burzynski
Research Institute in Houston. The medical records
of seven brain tumor patients who were thought to
have benefited from treatment with antineoplastons
were reviewed by NCI. This did not constitute a clinical
trial but, rather, was a retrospective review of medical
records, called a "best case series." The reviewers of
this series found evidence of antitumor activity, and
NCI proposed that formal clinical trials be conducted
to further evaluate the response rate and toxicity of
antineoplastons in adults with advanced brain
tumors."
These clinical trials never occurred. Nonetheless, the
Burzynski Research Institute is conducting FDA
approved clinical trials using antineoplastons for a
variety of cancers. Results in brain tumor continue to
be encouraging. In a March 2006 study published in
the journal Integrative Cancer Therapies, four patients
with glioblastoma were treated with antineoplastons.
One of the four patients had survived (at the time of
publication) more than 5 years. The results of only
four patients may not be statistically valid, but if they
are validated with further results it would suggest a 5-
year survival of 25% compared to 3.3% with
conventional therapies.
Are mainstream oncologists intrigued by the potential
therapeutic value of antineoplastons? No. Nearly all
oncologists reject this modality.
Conventional Oncologists Reject Unorthodox
Approaches
Why do oncologists reject any potential therapy, like
lipoic acid-palladium complex and Burzynski's
antineoplastons, that was not created by a major
medical center or a pharmaceutical company? There
are many reasons possibly including:
1) These approaches represent fundamental shifts in
thinking about how to treat brain cancer. To
understand how Poly MVA or antineoplastons may
work in the human body requires a different
understanding of the biochemistry of cancer and the
role of our immune systems.
2) The experience and skills of mainstream
oncologists are dictated to a large degree by what they
leaned in medical school and the studies they have
been involved in subsequent to their graduation.
These studies are often financed or partly financed by
drug companies who focus on therapies that are
easily patentable. Chemotherapy fits this model.
3) There may be an emotional investment. In the case
of malignant gliomas many oncologists have seen
hundreds of their patients pass away. To admit that
they, the doctor, have been on the wrong path all
along, maybe too tough to bear.
Whatever the reasons, the result has been no
dramatic improvement in survival with GBM over
decades. Because patients who are the ultimate
consumer of these therapies generally put their lives
in their doctor's hands, there is no "market demand"
for thinking outside the box. Because drug
companies finance the lion's share of research in this
area, corporations continue to decide what is
developed and what is not based on their own
financial incentives. Because doctors get paid
regardless of whether their patients live or die there is
no burning incentive for physicians to break from the
status quo. What all this means, unfortunately, is that
the lack of progress will most likely continue.
But, there is hope for Mr. Kennedy and other patients
diagnosed with malignant gliomas. If you are willing
to be your own best advocate and expand your
universe of possible treatment modalities outside of
chemo, radiation, and surgery, you may be able to
blaze your own path to health as others have done.
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