Bioenergetic Expert Warns Against Misguided Cancer Treatment Trends, Offers New Insights

Certain everyday exposures may quietly tilt your body toward a state of decline that feels almost impossible to notice. Left unchecked, this subtle imbalance can ripple through your system.

STORY AT-A-GLANCE

• Cancer occurs when cells abandon efficient mitochondrial energy production for glycolysis, creating lactic acid buildup and cellular dysfunction

• Estrogen drives cancer progression by forcing cells into glycolysis, while protective hormones like progesterone, testosterone, and pregnenolone counteract these harmful effects

• Environmental toxins including pesticides, plastics, soy, flax, and blue light waves act as endocrine disruptors, creating estrogen dominance and damaging mitochondrial function

• Standard cancer treatments like chemotherapy backfire by leaving cellular debris that triggers inflammation throughout the body, spreading the disease further

• Therapeutic approaches using aspirin, carbon dioxide, B vitamins, and hormone optimization restore healthy cellular energy production and guide damaged cells toward apoptosis

Advertisement

In an interview by the Rooted in Resilience podcast, bioenergetic researcher Georgi Dinkov provided an update on his research regarding the pitfalls of common cancer treatments, arguing that this approach often goes in the wrong direction. Instead of focusing on what fuels tumors, many doctors target hormones in ways that may worsen the disease.¹ He also discussed innovative strategies that result in better outcomes.

All these and more, are discussed in the podcast. I encourage you to listen to it, as it contains a wealth of new information that will change the way you think about cancer and the promising treatments that will be available in the future.

Why Do Cells Become Cancerous?

According to Dinkov, cancer is not just about random mutations, as mainstream medicine often teaches. Instead, he described it as your body falling back on an older, less efficient way of producing energy. But when stress or toxins push your cells to rely on it all the time, you are left with uncontrollable cells.

• Your cells cannibalize their own mitochondria — Dinkov described this change as your cells dismantling their mitochondria. Once those engines are taken apart, the cells start depending on a faster but dirtier process that leaves behind waste like lactic acid. This is what keeps the cancer state alive. The more your cells rely on this shortcut, the more likely they are to keep breaking down instead of functioning normally.

• Many cancer cells are not beyond saving — If you improve the cellular environment, your cells often return to normal energy production. This means that cancer, at least in its earlier stages, doesn’t always need to be attacked or destroyed. Instead, giving the cells what they need to repair themselves can turn them back into healthy, functioning tissue:

  “[I] recently was on another podcast with, Dr. [Thomas] Seyfried, who's the one who demonstrated that it's not the mutations that are causing the cancer. It’s the dysfunctional mitochondria. And his research, as well as mine, shows that you can reverse a cancer cell and make it normal again, but only in the circumstances where the mitochondria is not damaged completely.”

• What to do for cells that are too far gone — Dinkov said they should be guided toward a natural shutdown process called apoptosis. This is a built-in safety feature in your body that removes damaged cells. “If it's severely damaged and the cell can and should be forced to commit apoptosis, which is the controlled self-destruction,” he says.

The 2 Energy Pathways in Your Cells

Dinkov described how your cells rely on two different ways of making energy. The first is oxidative phosphorylation, which happens inside your mitochondria. This is the clean, high-powered method your cells are designed to use. The second is glycolysis, which takes place outside the mitochondria. Glycolysis is faster but much less efficient, producing only a small amount of energy along with a lot of waste products.

• When your cells begin depending mostly on glycolysis, trouble starts — Dinkov explained that glycolysis doesn’t just mean less energy — it also changes the chemistry inside the cell. The buildup of lactic acid pushes your cells into a more reductive state, which signals them to break down their mitochondria even further. The result is a downward spiral where the cells lose their ability to return to normal function.

• The breakdown in energy production is central to cancer behavior — According to Dinkov, glycolysis is meant as a backup for short-term survival, but cancer locks cells into that mode permanently. If the mitochondria are not working properly, cells become aggressive, multiplying rapidly.

• Restoring oxidative phosphorylation is the key to turning the tide — If you can push energy production back into the mitochondria, your cells have a chance to function normally again. But if the mitochondria are too badly damaged, then the better option is for those cells to self-destruct through apoptosis. Either way, focusing on mitochondrial health rather than simply blasting cells with drugs or radiation offers a different healing pathway.

How Estrogen Pushes Cancer Forward

Estrogen is a powerful force inside your body that changes how your cells make energy. Considering this, Dinkov argued that estrogen forces the cells to rely more on the backup system of glycolysis. This shift creates more lactic acid and weakens your mitochondria, pushing your cells toward a cancerous state.

• Other hormones balance your system — Progesterone, pregnenolone, testosterone, and dihydrotestosterone (DHT) provide a beneficial effect. Dinkov explained that these hormones help your cells resist estrogen’s effects by keeping energy flowing through the mitochondria.

• Here’s one example of how hormones protect against cancer — According to Dinkov, progesterone directly blocks estrogen’s activity at the cell level:

  “So, first of all, pregnenolone, progesterone, to a smaller degree, DHEA [Dehydroepiandrosterone], testosterone dehydrogenase — they're all aromatase inhibitors. So, they directly limit the synthesis of new estrogen no matter where it has been synthesized.

  Every cell expresses the aromatase enzyme, which is the rate-limiting step in synthesizing estrogen. So, anything that that inhibits aromatase, you know, basically will decrease the production of estrogen.”

The Hidden Threats Around You

The environment you live in is stealthily shifting your body’s chemistry in ways that increase your risk of cancer.

• Toxic chemicals all around you fuel cancer risk — Dinkov explained that pesticides, plastics, and even foods like soy and flax carry compounds that act like estrogen once they enter your body. These are known as endocrine disruptors, and according to him, they create a constant state of estrogen dominance.

• Blue light exposure fuels cancer — Dinkov pointed out that the vast majority of people are exposed to blue light via fluorescent bulbs, which affect your health:

  “Our mitochondria does not like blue light because blue light is toxic to bacteria, viruses, fungi, all these primitive microorganisms, which is probably another corroboration of the theory that mitochondria is originally, such an organism that fused with our primitive human cells because blue light is toxic to mitochondria as well.”

• Other side effects of blue light — Aside from increasing your risk of cancer, Dinkov noted that blue light affects your health in different ways. For example, if you sit under it for hours a day, such as being in an office, you’ll eventually develop headaches, cognitive disturbances and increased risk of mental health disorders.

Why Standard Cancer Treatments Might Backfire

As mentioned in the introduction, mainstream cancer treatments often create more harm than help. Dinkov explained that when doctors aggressively attack tumors with chemotherapy or radiation, the dying cells spill their insides into the bloodstream.

• Killed cancer put your immune system on overdrive — Once you kill cancer cells through pharmaceutical drugs, the debris acts like a danger signal to your body. The immune system reacts as if you are under attack from a major infection, spreading inflammation throughout your body. “A lot of the mitochondrial debris and the debris from the nucleus trigger the exact same pathways and receptors that bacteria or viral infections trigger,” he says.

• Inflammation shuts down your body’s preferred energy system — Oxidative phosphorylation takes a back seat. When that switch is flipped, healthy tissues across your body start acting more like cancer cells. “The entire body says, I’m under attack,” he explained, which pushes cells into the cancer metabolism instead of restoring balance.

  This helps explain why many people see their cancer return after initially successful treatments. Dinkov said that doctors are very good at killing the primary tumor, but the aftermath often leads to scattered, aggressive new tumors appearing throughout the body. He described this as turning “a million little cancers, and it’s all over the body” because the environment has been shifted into the wrong metabolic state.

• Returning cancer cells to normal before apoptosis — Instead of going to war with cancer right away, Dinkov suggested another path. He argued that cancer cells can be coaxed back to normal function if energy production is restored:

  “[M]ost cancer cells are still structurally normal, they are metabolically deranged, but they're still normal. Some of them are too damaged, but it looks like there's a small percentage. So really, the goal should be don't immediately go on an all-out assault, right, which, it turns out to be self-destructive. Try to coax the cancer cell to act normal again and that can be done metabolically with various approaches.”

Why the Latest Research Isn’t in Research Journals Yet

Dinkov noted that his latest research on cancer hasn’t made it into mainstream medical journals, explaining that publishing bold results often triggers powerful pushback. “You should be ready with lawyers because they’re going to attack,” he said, noting that once a controversial study is challenged and retracted, your ability to publish again is severely damaged.

• Simply share the information — Instead of chasing recognition, Dinkov said he focuses on getting information directly to people. He’s already received confirmation from doctors around the world who are quietly using his protocols. One oncologist in Ireland, for example, emailed him saying several patients had their surgeries canceled because their tumors had completely disappeared.

• Nefarious forces are pushing back — Dinkov also pointed out how easy it is for his research to be challenged. Powerful interests in the cancer industry could run the same experiments and report different results. If that happens, journals often retract the original paper, which damages the credibility of the scientists involved. That fear, he said, is one reason many professors refuse to publish such controversial work, even if the data looks strong.

• Big Pharma wants to preserve the status quo — Dinkov noted that even if human trials confirm his approach, powerful resistance will remain. Cancer treatment today is a massive industry, and anything that threatens its profit model faces enormous barriers. For him, the biggest confirmation may not come from journals but from a grassroots movement of patients and doctors who have proven results:

  “[I]f it works for sufficiently large number of people, then I don't need to publish. In fact, I don't care about publishing. Why do I need to give the enemies a sign that, you know, we're brewing a resistance here and the resistance is working?”

There Are Ways to Bring Cells Back Toward an Optimally Healthy State

There are several tools that can help your cells return to healthy energy production instead of staying locked in the cancer state. Dinkov goes over them throughout the course of the podcast:

• Aspirin — You might think of aspirin only for pain or fever, but Dinkov described how it works inside your cells to slightly lower their internal pH. This acidic environmental shift gives cells a choice — if they’re still repairable, they switch back to the healthier oxidative phosphorylation, but if they’re too damaged, they self-destruct through apoptosis.

• Carbon dioxide (CO₂) — When you increase CO₂ in your body, it moves through your cells like a current, carrying electrons and helping energy flow more smoothly. Dinkov described carbon dioxide as doing the opposite of lactic acid — it encourages proper energy production and slows down cancer metabolism:

  “[T]he acidic nature of the carbon dioxide molecule, it draws electrons across the cell as it moves, as it diffuses out of the cell. And that helps speed up the oxidative phosphorylation reaction. Also, carbon dioxide and lactate are inversely correlated in the body.”

• B vitamins — Vitamins B1 and B3 act as cofactors. Without them, the electron transport chain stalls out, and cells can’t make enough energy. In Dinkov’s research, combining aspirin with these nutrients restored energy flow in cells that had been struggling.

• Hormones — These include pregnenolone, which Dinkov described as the “structural cell stabilizer,” and testosterone. As mentioned earlier, progesterone blocks estrogen’s harmful effects as well. To learn how to use it properly and optimize your health, follow the instructions in the following sections.

How to Use Progesterone

Before you consider using progesterone, it is important to understand that it is not a magic bullet, and that you get the most benefit by implementing a Bioenergetic diet approach that allows you to effectively burn glucose as your primary fuel without backing up electrons in your mitochondria that reduces your energy production. My new book, "Your Guide to Cellular Health: Unlocking the Science of Longevity and Joy," covers this process in great detail.

Once you have dialed in your diet, an effective strategy that can help counteract estrogen excess is to take transmucosal progesterone (i.e., applied to your gums, not oral or transdermal), which is a natural estrogen antagonist. Progesterone is one of only three hormones I believe many adults can benefit from. (The other two are DHEA and pregnenolone.)

I do not recommend transdermal progesterone, as your skin expresses high levels of 5-alpha reductase enzyme, which causes a significant portion of the progesterone you're taking to be irreversibly converted primarily into allopregnanolone and cannot be converted back into progesterone.

Ideal Way to Administer Progesterone

Please note that when progesterone is used transmucosally on your gums as I advise, the FDA believes that somehow converts it into a drug and prohibits any company from advising that on its label. This is why companies promote their progesterone products as "topical."

However, please understand that it is perfectly legal for any physician to recommend an off-label indication for a drug to their patient. In this case, progesterone is a natural hormone and not a drug and is very safe even in high doses. This is unlike synthetic progesterone called progestins that are used by drug companies, but frequently, and incorrectly, referred.

Dr. Ray Peat has done the seminal work in progesterone and probably was the world's greatest expert on progesterone. He wrote his Ph.D. on estrogen in 1982 and spent most of his professional career documenting the need to counteract the dangers of excess estrogen with low-LA diets and transmucosal progesterone supplementation.

He determined that most solvents do not dissolve progesterone well and discovered that vitamin E is the best solvent to optimally provide progesterone in your tissue. Vitamin E also protects you against damage from LA. You just need to be very careful about which vitamin E you use as most supplemental vitamin E on the market is worse than worthless and will cause you harm not benefit.

It is imperative to avoid using any synthetic vitamin E (alpha tocopherol acetate — the acetate indicates that it's synthetic). Natural vitamin E will be labeled "d alpha tocopherol." This is the pure D isomer, which is what your body can use.

There are also other vitamin E isomers, and you want the complete spectrum of tocopherols and tocotrienols, specifically the beta, gamma, and delta types, in the effective D isomer. As an example of an ideal vitamin E, you can look at the label on our vitamin E in our store. You can use any brand that has a similar label.

You can purchase pharmaceutical grade bioidentical progesterone as Progesterone Powder, Bioidentical Micronized Powder, 10 grams for about $40 on many online stores like Amazon. That is nearly a year's supply, depending on the dose you choose.

However, you will need to purchase some small stainless steel measuring spoons as you will need a 1/64 tsp, which is 25 mg and a 1/32 tsp, which is 50 mg. A normal dose is typically 25 to 50 mg and is taken 30 to 60 minutes before bed, as it has an anti-cortisol function and will increase GABA levels for a good night's sleep.

If you are a menstruating woman, you should take the progesterone during the luteal phase or the last half of your cycle, which can be determined by starting 10 days after the first day of your period and stopping the progesterone when your period starts.

If you are a male or non-menstruating woman, you can take the progesterone every day for four to six months and then cycle off for one week. The best time of day to take progesterone is 30 to 60 minutes before bed as it has an anti-cortisol function and will increase GABA levels for a good night's sleep.

This is what I have been personally doing for over a year with very good results. I am a physician so do not have any problems doing this. If you aren't a physician, you should consult one before using this therapy, as transmucosal progesterone therapy requires a doctor's prescription.

Frequently Asked Questions (FAQs) About Cancer Growth and Treatment

Q: What drives cancer growth?

A: Bioenergetic researcher Georgi Dinkov explained that estrogen plays a central role in driving cancer by forcing cells into a backup energy process that produces lactic acid and weakens mitochondria. On the other hand, protective hormones like progesterone, pregnenolone, testosterone, and dihydrotestosterone (DHT) help balance the system by keeping energy flowing through mitochondria, making it harder for cancer to take hold.

Q: How does Dinkov view cancer compared to mainstream medicine?

A: Mainstream medicine often sees cancer as a problem of random mutations, but Dinkov described it differently. He said cancer is your body falling back on an old, inefficient energy system when mitochondria are damaged. Instead of being hopelessly broken, many cancer cells can be returned to normal if their environment is improved and healthy energy production is restored. Only the most damaged cells need to be removed through apoptosis.

Q: What role do mitochondria play in cancer?

A: Mitochondria are like the power plants of your cells. When they work well, they run on oxidative phosphorylation, an efficient way of making energy. But if stress or toxins damage them, your cells dismantle mitochondria and switch to glycolysis, a dirty backup process. This leads to lactic acid buildup, aggressive cell growth, and cancer behavior. Restoring oxidative phosphorylation gives cells the best chance to function normally again.

Q: How does the environment increase cancer risk?

A: Dinkov highlighted that the world around you is full of hidden stressors that push your cells toward cancer. Everyday chemicals such as pesticides, plastics, soy, and flax contain compounds that mimic estrogen, creating a constant hormonal imbalance. He also warned about blue light exposure from fluorescent bulbs and screens, which harms mitochondria, increases cancer risk, and contributes to headaches, mood issues, and even mental health problems.

Q: Why do common cancer treatments backfire?

A: Dinkov argued that aggressive treatments like chemotherapy and radiation shrink tumors but often make things worse overall. When large numbers of cancer cells are killed at once, they spill toxic debris into the bloodstream.

This triggers inflammation and shuts down oxidative energy production across the body, creating an environment where new, more aggressive cancers spread. Instead, he recommends supporting mitochondria so that repairable cells can return to normal, while the most damaged cells quietly shut down through apoptosis.

Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.

The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.

If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.

1. YouTube, Strong.Sistas, May 23, 2025