I (Reginald B. Little, RBL) am fully aware of how to test my theory and get very quick results. But I lack laboratory for such. If someone is interested in collaborating, then please contact me.

I (RBL) propose the following to give some quick rough data to determine if 13C stable isotope or carbon 13 is causing cancer and accelerating cancer as a follow up of the research at MD Anderson Cancer Center:

I notice that prior measurements performed in-vivo studies on the mice giving them d-fructose and d-glucose and saw the mix of d-fructose and d-glucose caused cancer to metathesize and become more malignant.  In these experiments according to Sigma-Aldrich the d-glucose and d-fructose were both derived from corn (C4) plant. This supports my theory of 13C causing and accelerating cancer as corn is a C4 plant and the fructose and glucose from corn are more enriched in 13C isotope that fructose and glucose from C3 plants like healthier fruits and veggies. So eating corn products from my prior theory is equivalent to daily infusing of 13C into the bodies of humans in equivalence to infusing 13C via corn glucose and fructose into the mice from this experiment with similar acceleration of cancer in the human host and faster metathesis of the cancer in the human to explain accelerating cancer in humans from diet and the accelerated metathesis in humans from sugary beverages by 13C isotope rather than fructose itself. But to ascertain this a control is needed of measuring the metathesis of the cancer in diet of lower 13C in the fructose and glucose. Therefore, I recommend:

1) I am interested in a similar experiment to compare with the published MD Anderson Cancer study involving in-vivo experiment but feeding the mice d-fructose and d-glucose from a C-3 plant.  I am wondering if the C3 plant having less than 13C would affect the metathesis (I think it may decrease the metathesis relative to the C4 glucose and C4 fructose, which have more 13C isotopes!).

2) A second in-vivo experiment would involve feeding the mice the isotope heavily labeled 13C6 fructose and 13C6 glucose (where all 6 carbons in the sugars are 13C) to see if the greater content of 13C accelerated the malignancy and metastasis.

It could also be that the heavy labeling by 13C kills the cancer. I think it may accelerate the cancer but under some conditions I propose the 13C can kill the cancer and give new basis for selective treatment.

For instance, I predict the heavily enriched 13C in cancer in vivo in patients afford irradiating the patient with anti-neutrinos by shielding the patient and placing near a nuclear reactor. The heavy shielding protects the patient from the deadly radiation, but the neutrinos pass straight thru the shielding. But by my prediction whereas the neutrinos do not interact with the shielding, the neutrinos interact with the 13C in the cancer cells in the patient to disrupt the cancer and possibly kill the cancer throughout the patients' bodies.

I know many people will be negative and receive my theory with harsh criticism, but I continue thinking and creating so long as I find virtue of possibly helping humanity and reducing human suffering and healing (I am true) in love and compassion for humanity. - Reginald B. Little