West Lafayette, Indiana
December 15, 2004
The form of
vitamin E found in many plant seeds – but not in most
manufactured nutritional supplements – might halt the growth of
prostate and lung cancer cells, according to a Purdue University
study.
A team led by Qing
Jiang (pronounced "ching zhang") has found that
gamma-tocopherol, which occurs naturally in walnuts, pecans,
sesame seeds, and in corn and sesame oils, inhibits the
proliferation of lab-cultured human prostate and lung cancer
cells. The vitamin's presence interrupts the synthesis of
certain fatty molecules called sphingolipids, important
components of cell membranes. However, the gamma-tocopherol
leaves healthy human prostate cells unaffected, which could give
it value as an anticancer agent.
"This is the first
time gamma-tocopherol has been shown to induce death in
lab-grown human cancer cells while leaving healthy cells alone,"
said Jiang, who is an assistant professor of foods and nutrition
in the College of Consumer and Family Sciences. "This could be
wonderful news for cancer patients if the effect can be
reproduced in animal models. But because most nutritional
supplements contain only alpha-tocopherol, a different form of
vitamin E that alone does not have these anticancer properties,
it may be better to supplement the diet with mixed forms of
vitamin E. The study shows that the anticancer effect is
enhanced when mixed forms are used."
Jiang's research
appears in the current (week of Dec. 13) online edition of the
scientific journal Proceedings of the National Academy of
Sciences. She co-authored the paper with Jeffrey Wong,
Henrik Fyrst, Julie D. Saba and Bruce N. Ames of the Children's
Hospital Oakland Research Institute in Oakland, Calif.
Scientists have
been studying vitamin E for more than three-quarters of a
century, but most efforts have focused largely on
alpha-tocopherol, one of eight known forms in the vitamin's
family. Alpha-tocopherol was found early on to have the most
beneficial effects on laboratory animals fed diets deficient in
vitamin E, and also is the major form found in body tissues. For
these reasons, it has been nearly the only form of the vitamin
to be included in most manufactured nutritional supplements.
"Since then,
alpha-tocopherol has justifiably earned a good reputation as an
antioxidant, which helps to fight against damage caused by
unwanted free radicals," Jiang said. "But its familiarity has
perhaps attracted research away from the other seven forms of
vitamin E, and since gamma-tocopherol is the vitamin's most
commonly occurring natural form in the American diet, I grew
interested in it a few years ago."
In 2000 another
study by Jiang and colleagues found that gamma-tocopherol
inhibits inflammation, which had already been implicated in
cancer development. They theorized that it might retard the
progress of cancer and cardiovascular disease, and to test their
hypothesis they exposed cultures of cancerous prostate and lung
cells to the vitamin. Normal prostate epithelial cells were used
as a control group.
"We discovered
that as we increased the quantity of gamma-tocopherol, the
cancer cells grew more slowly," Jiang said. "But the normal
prostate cells were not affected and grew normally. This could
indicate that the vitamin could be used to target lung and
prostate cancer cells without the damaging side effects of
chemotherapy."
The study also
revealed that gamma-tocopherol caused cell death by interrupting
sphingolipid synthesis.
"This is also a
novel discovery," Jiang said. "Although there have been prior
indications that some form of vitamin E may cause cell death in
some mouse cell lines, we are the first to provide a mechanism
for such an effect."
Gamma-tocopherol,
though rarely available in vitamin pills, is nevertheless found
in abundance in the typical American diet. Many nuts are rich in
it, including walnuts and pecans, as are cooking oils such as
corn and sesame oil.
Though Jiang said
she would be cautious about using food sources to slow prostate
or lung cancer's progress in humans, she said that high-risk
groups such as older men could benefit from supplementation – if
carried out with prudence.
"Foods rich in
gamma-tocopherol are also rich in fats, and some products bring
other hazards as well," she said. "Corn oil, for example, is
rich in linolic acid, which has been shown to promote certain
types of cancer in some studies. But sesame seeds and pecans
seem to be good all-around choices."
Jiang said the
next step for her research team would be testing the effect of
gamma-tocopherol and mixed forms of vitamin E on animal cancers.
"Although this
discovery is promising, we do not yet know whether
gamma-tocopherol has any effect on cancer in living creatures,"
she said. "We hope that future research not only will clarify
whether gamma-tocopherol could have applications in human cancer
treatment, but also will show how we might supplement the body
with the vitamin to prevent cancer from developing in the first
place. These questions will continue to direct our work."
This research was
funded in part by the National Institutes of Health.
Writer:
Chad Boutin
Related Web site:
Online paper in Proceedings of the National Academy of Sciences
ABSTRACT
Gamma-Tocopherol
or Combinations of Vitamin E Forms Induce Cell Death in Human
Prostate Cancer Cells by Interrupting Sphingolipid Synthesis
Qing Jiang, Jeffrey Wong,
Henrik Fyrst, Julie D. Saba, and Bruce D. Ames
g -Tocopherol (g
T), the predominant form of vitamin E in diets, but not a
-tocopherol (a T), the major vitamin E form in tissues and
supplements, inhibits proliferation of prostate (LNCaP, PC-3)
and lung (A549) cancer cells. In contrast, at similar
concentrations, g T had no effects on normal prostate epithelial
cells. Combinations of some vitamin E forms such as g T and d
-tocopherol (d T) exhibit additive or synergistic inhibitory
effects. g T, and its combination with d T, induced apoptosis in
androgen-sensitive prostate LNCaP, but not androgen resistant
PC-3 cells, by the induction of cytochrome C release, activation
of caspase 9 and caspase 3, cleavage of PARP and involvement of
caspase-independent pathways. Myriocin and fumonisin B1,
specific inhibitors of key enzymes (serine palmitoyltransferase
and dihydroceramide synthase, respectively) in de novo
synthesis of sphingolipids, significantly protected cells from g
T-induced DNA fragmentation, cytochrome C release, PARP cleavage
and the formation of active caspase 3. Compared with
vehicle-treated controls, g T treatment led to pronounced
dihydroceramide and dihydrosphingosine accumulation, which
preceded morphological and biochemical manifestations of
apoptosis. In contrast, ceramide levels did not increase until
day 3, when substantial cell death took place. Our study
demonstrates that g T and mixed vitamin E forms induce cell
death by interrupting the de novo sphingolipid pathway in
a prostate cancer cell line. Thus, certain vitamin E forms may
be valuable as anticancer agents. |