Comments by "Roger Scott Cathey" (@rogerscottcathey) on "To Be Frank" channel.

  1. 2
  2. 2
  3. 2
  4. 2
  5. 2
  6. 2
  7. 2
  8. 2
  9. 2
  10. 2
  11. 2
  12. 2
  13. 2
  14. 2
  15. 2
  16. 2
  17. 2
  18. 2
  19. 2
  20. 2
  21. 2
  22. 2
  23. 2
  24. 2
  25. 2
  26. 2
  27. This surgical gymnastics sounds like a good alternative for now from cut, burn and poison alright. But it is akin to "fecal transplant". There HAS to be a better way. For cancer there is the much simpler Lambelle treatment of IM injection of amylase and trypsin. The cancer cell is protected from white blood cells by electronegative sialylated proteins. The glycoprotein is well known: chorionic gonadotrophins, or hCG. White blood cells carry the same charge, they cannot approach. However amylase immediately deactivates hCG by direct digestion or hydrolyzation of the sialylated carbohydrate moiety of hCG. Trypsin, tryptase and RNAse also set to work thereafter. The hCG cell wall motif is characteristic of only one normal cell in the life cycle: trophoblasts. That is how we know cancers are trophoblastic, as fully confirmed by thousands of biopsies and clonal cultured cell lines by flow cytometry analysis, and genotyping. See the seminal article on this by Hernan Acevedo in the 1995 issue of Cancer, if memory serves. As all cancers, regardless of type or origin are trophoblastic, we know they have only one source: diploid totipotent cells, i.e., stem cells. Outside pregnancy, stem cells are only active in regeneration and healing. They are most active in the gut, pancreas and liver, but are obviously active wherever cancer can be observed. Even brain contain active stem cells. When trophoblastic differentiation arises normally in the life cycle, it is as placenta. It mediates the nutrition of the stem cell package. In healing it obviously must play a role in regeneration. If hayflick limited cell lines need replacing it is not enough to have cells crowd them out, the old cells need removal. White blood cells only remove dead and apoptotic signaling cells. Only trophoblasts are known to do this. They are highly mobile, invasive and thus metastatic by nature. They cannot dedifferentiate, they are the most primal differentiated cell and the least pluripotent cell. The stem cell can evoke trophoblast to accomplish its needs, but trophoblast cannot evoke stem cells. In the normal model of function, trophoblast begin to be degraded in the 8th or 9th week of pregnancy, at the onset of fetal pancreatic function. The fetal pancreas secretes no amylase, but his mother's amylase titers continuously increase until parturition. The dual action of fetal and maternal amylase and the serine proteases degrade the trophoblast hold on the syncytium in the limb of uterus until it releases. The hypoxic conditions of syncytiotrophoblasts in the interface induces anaerobic metabolites to permeate soma inducing the oxytocin cascade inducing contraction to expell. The clues to cancer resolution need only mimic the normal precedent in the cause of birth.
    2
  28. 2
  29. 2
  30. 2
  31. 2
  32. 2
  33. 1
  34. 1
  35. 1
  36. 1
  37. 1
  38. 1
  39. 1
  40. 1
  41. 1
  42. 1
  43. 1
  44. 1
  45. 1
  46. 1
  47. 1
  48. 1
  49. 1
  50. 1