Just learned about another exciting anti-cancer nutrient – Cancer Defeated

Just learned about another exciting anti-cancer nutrient

By Lee Euler / February 12, 2017

What is it about fresh fruits and vegetables that makes them so good for us? Can nature’s bounty really be that tuned in to what the human body and mind needs to stay healthy?

As it turns out… yes.

The longer researchers study plants, fruits and vegetables the more phytonutrients — plant-based chemicals proven to have health benefits for humans –they discover.

These phytonutrients can be used as treatments for various conditions ranging from Alzheimer’s disease to cancer.

I recently came across a new one that shows great promise in treating a variety of cancers…

I’m talking about fisetin, a flavonal that belongs in the flavonoid group of nutrients.

Flavonoids exhibit a range of biological properties including antioxidant, anticarcinogenic, anti-inflammatory, antibacterial, antiviral and immune-stimulating effects.1

Other flavonoids include chemicals previously covered in this newsletter such as quercetin, kaempferol, and catechins.

Fisetin is found in many plants, fruits and vegetables and acts as a coloring agent (as the best plant nutrients often do.) Once eaten, it can have a powerful effect on the body. It chews up free radicals, reduces inflammation and destroys cancer cells while leaving healthy cells unharmed.

Prevents cancer before you get it,
treats cancer after you have it

Researchers are interested in how fisetin works when eaten and how its chemopreventive and chemotherapeutic properties can be synthesized to create new treatment options for cancer.

They’ve learned that fisetin can inhibit the growth of cancer cells by altering the cell cycle and inducing apoptosis (programmed cell death).2

Below is a small sampling of the research. . .

Lung cancer

Lung cancer is one of the most common cancers in the world, and metastatic lung cancer is the cause of more than 90% of deaths related to lung cancer.3

A 2009 study published in the Journal of Agricultural and Food Chemistry found that fisetin inhibited the migration and invasion of A549 cells — in other words, the spread of a particular kind of lung cancer cell.

Fisetin also interfered with the cells’ signaling ability, which further reduces the spreading and metastasis of the cancer. These facts lead the researchers to conclude that fisetin plays a significant role in reducing invasion and migration of these deadly cells.4

A hydrocarbon called benzo(a)pyrene [B(a)P] plays a key role in lung carcinogenesis caused by tobacco smoke.5

Research published in the journal Food and Chemical Toxicology shows that treatment with fisetin “significantly reduced” the degree of lesions in the lungs and increased antioxidant levels in B(a)P-induced mice.

Fisetin also showed an anti-proliferation effect against the lung cancer cells, reducing the spread of the disease.6

Colon cancer

A lot of research has been done around flavonoids and colon cancer, because it’s well established that eating or not eating certain foods plays an important role in reducing the risk of this type of cancer.7

It makes sense that what a person eats would affect their colon, right?

A common cause of colon cancer is the overexpression of cyclooxygenase 2 (COX2) and uncontrolled signaling pathways. You’ve probably heard of COX2 because it’s a well-known cause of inflammation. A 2009 study found that treatment with fisetin on the overexpressing cells resulted in apoptosis and downregulating of COX2 protein expression.

The activity of the signaling pathways also decreased, thereby decreasing the spread of the cancer cells.8

Prostate cancer

Research shows an inverse relationship between the amount of flavonoid intake and prostate cancer risk. An example of this is that the East Asian diet is high in flavonoids, and men in China and Japan have the lowest incidence of prostate cancer worldwide.

Fisetin in particular has shown antiproliferative and cell cycle arresting properties when applied to prostate cancer cells.9

In addition to that, fisetin has also shown promise in regulating the signaling pathways that run out of control in prostate cancer, as well as inducing programmed cell death.10

Other cancers

In much the same ways as mentioned above (inducing apoptosis, regulating cell signaling pathways), fisetin has shown promise in treating pancreatic cancer11, melanoma12, and gastric cancers.13

Get your fisetin here

Now that we’ve seen how beneficial this flavonoid is, I’m sure you’re wondering how you can get more of it in your diet.

Fisetin is found in abundance in fruits and vegetables such as:

✔  Strawberries

✔  Blueberries

✔  Mangoes

✔  Apples

✔  Persimmon

✔  Kiwi

✔  Grapes

✔  Onions

✔  Cucumber

The skins of these foods contain high levels of fisetin, so whenever possible be sure to eat these foods whole.

When eating the skins of fruits and vegetables your best bet is to buy organic, especially if it’s a food (such as strawberries) that’s high on the Environmental Working Group’s (EWG) Dirty Dozen list — a list of the foods most contaminated by chemical and industrial pesticides. Apples and grapes are also on the list.14

Fisetin is also available in supplements. Most doses are around 100 mg per day, and you shouldn’t need more than that.

The research I’ve seen didn’t mention any adverse effects of getting too much fisetin, but that doesn’t necessarily mean more is better. So take the supplement only as directed.

Better yet, be sure to eat your organic fruits and vegetables for good overall health and reduced cancer risk.

Plant remedies are wonderful, but drugs aren’t all bad. Last issue I wrote about one that l think is an important cancer treatment. If you missed it, we’re running the article again just below.

Inexpensive, Off-Patent Drug Turns Out to be
A Cancer Game-Changer

“. . .every day I am thankful to have the opportunity
to watch the responses as they happen.” – Dr. Jill Cottel

Dr. Angus G. Dalgleish, professor of oncology at St George’s Hospital, London, was very surprised to see an advanced cancer patient’s condition had remained stable, so he asked her if she was using a remedy he didn’t know about.

She admitted she was taking low-dose naltrexone (LDN).

After coming across other patients doing well on LDN, Dr. Dalgleish decided to prescribe it for patients who had run out of all conventional options. Here’s what he found. . .

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Dr. Dalgleish describes some of the results he has witnessed as “clearly quite remarkable.”

One of his patients had a very serious melanoma of the head and neck. He’d been stable on an immunotherapy program for four years, but then his condition started to progress. He wouldn’t accept chemotherapy, but agreed to take LDN.

Within a week, he broke out in severe whole body vitiligo (white skin patches). The patient wasn’t pleased, but Dr. Dalgeish was delighted.

That’s because the skin symptom showed that part of the patient’s immune receptor pathway was being stimulated and had targeted the melanoma. The immune system’s killer T cells had started to recognize a major component of melanoma – melanin – and were taking out the normal melanin at the same time. This “side effect” created the bare skin patches.

What state-of-the-art, orthodox cancer treatment hadn’t achieved in four years, LDN attained in a matter of days. The patient is still alive some years later.

Dr. Dalgleish’s other experiences include:

  • multiple liver metastases in patients who went on to long-term disease-free status or stability
  • stabilization of advanced ovarian cancer
  • stabilization of advanced prostate cancer
  • stabilization of stage IV glioma (a brain cancer) for six months, even though the patients had continued to go downhill during standard radiotherapy and chemotherapy
  • remarkable improvements in the mental state of patients. They feel much better, probably due to subtle effects on opiate receptors

Immunomodulatory Effects

Naltrexone belongs to a family of drugs called opiate antagonists. These block the activity of many naturally occurring chemicals such as neurotransmitters and hormones. It was licensed as a treatment for drug and alcohol addiction in 1984 in dosages ranging from 50mg to 300mg.

It may seem odd, but a medication used to help drug addicts kick the habit turns out to be a powerful anti-cancer remedy. I first wrote about LDN years ago, and my enthusiasm only continues to grow.

It’s effective because the body produces its own natural opiates called endorphins, well known for giving feelings of euphoria, and these have an important immune function. Naltrexone has endorphin-modifying properties.

An influential paper written in 1985 concluded that “endorphins can be considered as immunomodulators…and may become a tool in the field of immunotherapy.”

As an endorphin modifier, naltrexone was found to have immunological effects at doses ten to forty times lower than that required for opiate or alcohol addiction.

In 1986, it was shown that receptors for opiates were present in many different types of immune cell. Since then, Dr. Ian Zagon from Pennsylvania State University has been at the forefront of work on endorphins and low-dose Naltrexone, publishing over 300 papers.

Works on many different facets of the immune system

Dr. Zagon has shown that the immune system is regulated by endorphins which act on opiate receptors. Blocking these receptors for a short time, by using LDN, upregulates the production of endorphins. These can act as immune modulators to correct immune system over- or under-functioning.

In addition, the growth of cells can also be suppressed by endorphins. This would clearly have applications in cancer treatment.

Endorphins are not the whole picture, however. LDN also binds to another group of receptors called toll-like receptors (TLRs) which are an essential part of the innate (non-specific) immune system. This function of the immune system provides a first-line defense against microbial invasion.

By binding to TLRs, LDN suppresses pro-inflammatory cytokines and NF-kB. The latter is a very potent molecule linked to the expression of cancer oncogenes. These in turn prevent cancer cells from self-destruction, leading to uncontrolled growth.

LDN has also been shown to increase natural killer cell and T lymphocyte activity, interfere with cell signaling, and increase p16 and p21 protein pathways to inhibit cancer cell division.

It’s a “game-changer”

One of the St. George’s research team, Dr. Wai M. Liu, says the beauty of LDN is that it is a fantastic stimulator of the immune system and is also able to bind to certain proteins on the surface of the cancer cell. It may even enter the cell independently of these receptors.

By doing so, it makes cancer more sensitive to cell death. This allows some other remedy to directly kill the cancer cell. LDN therefore is best used as an adjuvant, in partnership with a direct cancer-killing agent.

In their most recent study, published in the International Journal of Oncology in August, 2016, they discovered in their lab work that continuous treatment with LDN had minimal effect on suppressing tumor growth in various cell lines.

However, changing the schedule to intermittent administration resulted in greatly enhanced cell destruction.

According to Dr. Liu, thanks to better knowledge of LDN’s impact on the immune system and results of their latest study, “we can design new treatment regimens; different strategies that can be used in patients, and in that regard it’s a game-changer because we now know how best to use LDN.”

Dr Bihari’s success with LDN

The first placebo-controlled, double-blind, randomized trial on LDN is due to report this year. However this study is restricted to measuring quality of life of glioma patients undergoing standard chemoradiation.

So we have to rely on anecdotal or small series evidence to see effects outside of the laboratory.

A pioneer in the use of LDN was the late Dr. Bernard Bihari, who practiced in New York. He is reported to have had considerable success among the 450 cancer patients that he saw.

86 experienced tumor shrinkage of at least three-quarters, with 125 stabilized and/or moving toward remission. These are impressive results, considering that many patients had already undergone standard treatments, and had run out of options. In addition, standard chemotherapy does tremendous damage to the immune system. It’s remarkable that LDN is able to revive immunity in these patients.

The experience of other doctors

Dr. Paul Anderson, Medical Director of AMSA Seattle, has been using LDN for eight years. The reason?

“I would say that of all the integrative and standard therapies that I have seen both in chronic illness, but especially in cancer, in the last 20 years, LDN has been one of the top treatments that has impressed me as far as outcomes, improving quality of life and stabilizing disease.”

LDN is also one of the treatments employed by Dr. Akbar Khan of the Medicor Cancer Center in Toronto. He started using it in 2007, and has continued to do so because he sees better patient outcomes.

Consider a few examples from his files:

  • 65-year-old with aggressive bladder cancer. Surgeons wanted to remove the bladder but he refused. He was put on LDN together with an immune therapy called BCG. After four months there was no trace of the tumor. He is still in full remission seven years later.
  • A 58-year-old presented with a rare form of mouth cancer. Surgeons recommended removal of tongue and voice box followed by chemoradiation. The patient refused such a mutilating strategy. He was prescribed LDN and high-dose vitamin D. Two years later, MRI scans showed complete disappearance of the cancer. He has now been cancer free for over five years.

Dr. Dana Flavin of the CollMed Foundation, Greenwich, Connecticut, says “all cancer patients should be on LDN because of the fact that it is helpful for them in every area of cancer therapy, period. If I had cancer myself I would be on LDN, and I’m a physician, pharmacologist and a former FDA official. I would recommend it to any and every one of my patients.”

Besides cancer, LDN is used for multiple sclerosis and lupus, inflammatory bowel disease, chronic fatigue syndrome and fibromyalgia, autoimmune thyroid disorders, restless leg syndrome, depression, and autism spectrum disorder.

Dr. Jill Cottel, medical director of the Poway Integrative Medicine Center in California, currently has more than 100 patients taking LDN. She writes:

“Not everyone has had a dramatic response, but there are many who have. Some of my patients became symptom-free within just a few months of treatment. Some of my chronic pain patients were pain-free within the first month.

“It has been an amazing thing to witness, and every day I am thankful to have the opportunity to watch the responses as they happen.”

I have seldom seen doctors rave about a cancer treatment like they do this one. It’s worth your attention.

LDN is a generic off-label prescription drug that is extremely safe. It has a low incidence of side effects, and those that occur usually resolve within a few weeks.

Every doctor in the US is able to prescribe it – if they are willing to do so.

Best regards,

Lee Euler,

References Article #1:
1 Fisetin: A dietary antioxidant for health promotion.
2 Dietary flavonoid fisetin for cancer prevention and treatment.
3 Lung cancer: Epidemiology, etiology, and prevention.
4 Involvement of the ERK signaling pathway in fisetin reduces invasion and migration in the human lung cancer cell line A549.
5 Benzo(a)pyrene induced lung cancer: Role of dietary phytochemicals in chemoprevention.
6 Fisetin, a novel flavonol attenuates benzo(a)pyrene-induced lung carcinogenesis in Swiss albino mice.
7 Fisetin: A dietary antioxidant for health promotion.
8 A plant flavonoid fisetin induces apoptosis in colon cancer cells by inhibition of COX2 and Wnt/EGFR/NF-kappaB-signaling pathways.
9 Novel antiproliferative flavonoids induce cell cycle arrest in human prostate cancer cell lines.
10 Fisetin induces autophagic cell death through suppression of mTOR signaling pathway in prostate cancer cells.
11 Fisetin, a natural flavonoid, targets chemoresistant human pancreatic cancer AsPC-1 cells through DR3 mediated inhibition of NF-κB.
12 Inhibition of human melanoma cell growth by dietary flavonoid fisetin is associated with disruption of Wnt/β-catenin signaling and decreased Mitf levels.
13 Fisetin inhibits cellular proliferation and induces mitochondria-dependent apoptosis in human gastric cancer cells.
14 Dirty Dozen.
References Article #2:
The LDN Book edited by Linda Elsegood
About the author

Lee Euler

Hi I'm Lee Euler, I’ve spent over a decade investigating every possible way a person can beat cancer. In fact, our commitment to defeating cancer has made us the world’s #1 publisher of information about Alternative Cancer Treatments -- with over 20 books and 700 newsletters on the subject. If you haven't heard about all your cancer options, or if you want to make sure you don’t miss even one answer to this terrible disease, then join our newsletter. When you do, I'll keep you informed each week about the hundreds of alternative cancer treatments that people are using to cure cancer all over the world.

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