Repurposing Drugs for Cancer Treatment
Once you put the patient in this state of nutritional ketosis, it
opens up a whole array, a new array of drugs that may have
been, uh, thrown out, not worked. That's called the whole field of
repurposing
drugs now.
Mm.
But once the body is in this new physiological state, things that were
thought to be ineffective become super effective.
So again, that's a whole new field that will open, uh, as the
results once this information gets out more.
And you mentioned, um, albendazole in your talk as well.
Does that have a, a, a glutamine blocking aspect to it as well?
Yes, that's in our paper also. That's another interesting thing.
Parasite medications. I don't know about ivermectin because
there was a lot
of political stuff about that. So I didn't-- I said to the, the lab,
"We're not gonna do that," because we didn't wanna get, get,
uh, get the wrath from somebody. But, but albendazole,
fenbendazole,
um, I said, "Why the hell... Why..." People have taken that and they,
and you hear
people say, "Well, I got my rid of my cancer with this
and that." So I, I,
I did a dive on it and I said, "Why, why parasite medications work
against cancer cells?"
And it turns out that the parasites use mitochondrial
substrate-level phosphorylation in the tissue.
And the, and these albendazole, fenbendazole kill these
parasites.
So I tried it on the cancer cell, and sure, sure as hell, they, it, it
targets the mitochondrial substrate and glycolysis.
Mm.
So we have a mechanism now why parasite medications are working.
But cancer is not a parasite.
Mm.
All these people say cancer is a parasite. It's not a parasite.
Parasites and tumors use a common metabolic pathway, and a drug that
works against parasites can be very effective against cancer,
and that's what we
begin to see, especially under nutritional ketosis.
Yeah.
Right? Can you imagine this?
Yeah. Yeah, that-- Oh, sorry, go on.
Um, so ivermectin, it actually works on the mitochondrial
cell death
pathway, the Bcl-2/Bax, Bad pathway.
So it actually helps push the cell death pathway.
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