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A few weeks ago, I released two videos
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on the general effectiveness of chemotherapy.
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What happens when you add fasting to the mix?
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This is the first of a 3-video series exploring that very question.
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"Fasting Before and After Chemotherapy and Radiation"
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For the past 50 years, chemotherapy has been a major medical treatment
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for a wide range of cancers.
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Its main strategy has been largely based on targeting cancer cells,
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by means of DNA damage caused in part by the
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production of free radicals.
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Although these drugs were first believed to be
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quite selective for tumor cells,
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we now know that normal cells also experience severe
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chemotherapy-dependent damage, leading to dose-limiting side effects
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including bone marrow and immune system suppression,
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fatigue, vomiting, diarrhea, and in some cases even death.
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And if you do survive, the DNA damage to normal cells
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can even lead to new cancers down the road.
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There are cell-protecting drugs that have been tried
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to reduce the side effects,
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so you can pump in higher chemo doses,
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but these drugs have not been shown to increase survival,
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in part because they may also be protecting the cancer cells.
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What about instead using fasting
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for cellular protection during cancer treatment?
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Fasting may have an unrecognized role
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in cancer prevention and treatment.
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Short-term fasting before and immediately after chemotherapy
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may minimize side effects, while at the same time
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may actually make cancer cells more sensitive to treatment.
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That's exciting.
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During nutrient deprivation, healthy cells switch from growth
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to maintenance and repair, but tumor cells are unable
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to slow down their unbridled growth due to growth-promoting mutations
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that led them to become cancer cells in the first place.
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This inability to adapt to starvation may represent an important
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Achilles' heel for many types of cancer cells.
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As a consequence of these differential responses
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of healthy versus cancer cells to short-term fasting,
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chemotherapy causes more DNA damage and cell suicide
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in tumor cells, while potentially leaving healthy cells unharmed.
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Thus, short-term fasting may protect healthy cells
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against the toxic properties of chemotherapy
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and render tumor cells more sensitive,
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or at least that's the theory. Let's test it out.
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Tyrosine kinase inhibitors are a group of chemo drugs
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that are now the mainstay of treatment in many types of cancer.
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Let's see them in action.
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These are petri dishes filled with cancer cells that
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have been dyed pink.
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Two types of lung cancer cells and one type of colorectal cancer.
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This is the before, and this the after, exposed to the chemo drugs
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erlotinib, gefitinib, crizotinib, and regorafenib.
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See how there's less pink?
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That shows how many cancer cells the chemo killed off.
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Starve the cells for 24 hours first, though,
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and the drugs work even better.
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Even the starvation alone without the drugs killed off a bunch of them.
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The researchers conclude that these TKI drugs that are
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commonly administrated for treating solid tumors become
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potentiated in their activity by 24 hours of starvation,
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but that's in a petri dish.
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Similar results were found for breast cancer and
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a chemo drug called doxorubicin.
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Here's five days of unhindered growth of breast cancer in a petri dish,
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from 150,000 cancer cells to 800,000 in under a week.
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Dripping on a little chemo can knock it down to around 600,000,
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but starve those cells for 48 hours first,
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and the chemo can completely keep them in check.
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Even the short-term starvation alone can restrain growth.
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Short-term fasting raises the possibility that you could get
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twice the effect for half the dose, which may be particularly important
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for a drug as toxic as doxorubicin, which causes heart failure
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in as many as 1 in 3 at higher doses.
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Again, though, these are just in vitro studies in a petri dish
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Then researchers moved to mice and found the same dual benefit:
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less toxic chemo, yet at the same time
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more effective, and not just by a little.
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A high enough chemo dose to kill 100% in less than a week.
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But after being starved for 60 hours, after the same dose, 100% survived.
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Ok, that's the toxicity. What about efficacy?
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Here's tumor growth without chemo, growth with chemo,
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and with chemo after short-term fasting,
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and this translated into improved survival.
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Interestingly, fasting alone appeared to work
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as well as the chemo, and the same with radiation.
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Unbridled tumor growth knocked down by radiation therapy,
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and even more so after the combination of radiation
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and alternate-day fasting,
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but alternate-day fasting alone seemed to do as well as the radiation.
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OK, but that's breast cancer in mice.
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I'm sure Mickey is thrilled for Minnie, but what about in people?
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We'll explore that next.
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