Thursday, September 20, 2018

100 Natural Anti-Cancer Substances

  1. AHCC ๐Ÿ›ˆ
  2. Allicin ๐Ÿ›ˆ
  3. Aloe Vera ๐Ÿ›ˆ
  4. Andrographis extract ๐Ÿ›ˆ
  5. Anthocyanin ๐Ÿ›ˆ
  6. Apigenin ๐Ÿ›ˆ
  7. Artemisinin ๐Ÿ›ˆ
  8. Ashitaba ๐Ÿ›ˆ
  9. Ashwagandha ๐Ÿ›ˆ
  10. Astragalus ๐Ÿ›ˆ
  11. Berberine ๐Ÿ›ˆ
  12. Beta-Glucan ๐Ÿ›ˆ
  13. Betulin ๐Ÿ›ˆ
  14. Bee Propolis ๐Ÿ›ˆ
  15. Bicarbonate ๐Ÿ›ˆ
  16. Bitter Melon ๐Ÿ›ˆ 
  17. Black cumin seed oil ๐Ÿ›ˆ
  18. Boswellia ๐Ÿ›ˆ
  19. Bovine Tracheal Cartilage ๐Ÿ›ˆ 
  20. Butyrate ๐Ÿ›ˆ 
  21. Caffeic acid ๐Ÿ›ˆ
  22. Calcium D-glucarate ๐Ÿ›ˆ 
  23. Cannabis ๐Ÿ›ˆ 
  24. Capsaicin ๐Ÿ›ˆ 
  25. Chaga ๐Ÿ›ˆ
  26. Chlorogenic acid ๐Ÿ›ˆ 
  27. Chrysin ๐Ÿ›ˆ
  28. Citric Acid ๐Ÿ›ˆ 
  29. Citrus Pectin ๐Ÿ›ˆ
  30. Coenzyme Q10 ๐Ÿ›ˆ
  31. Coumaric acid ๐Ÿ›ˆ
  32. C-phycocyanin ๐Ÿ›ˆ
  33. Cranberry ๐Ÿ›ˆ
  34. Curcumin ๐Ÿ›ˆ
  35. Danshen ๐Ÿ›ˆ 
  36. D-Limonene ๐Ÿ›ˆ
  37. Epigallocatechin-3-gallate ๐Ÿ›ˆ 
  38. Ellagitannins ๐Ÿ›ˆ 
  39. Enzymes ๐Ÿ›ˆ
  40. Evodiamine ๐Ÿ›ˆ
  41. Fisetin ๐Ÿ›ˆ
  42. Fucoidan ๐Ÿ›ˆ
  43. Galangal ๐Ÿ›ˆ
  44. Garcinol ๐Ÿ›ˆ 
  45. Ginger ๐Ÿ›ˆ
  46. Ginko Biloba ๐Ÿ›ˆ
  47. Graviola ๐Ÿ›ˆ
  48. Grape Seed Extract ๐Ÿ›ˆ
  49. Hericium Erinaceus extract ๐Ÿ›ˆ
  50. Honokiol ๐Ÿ›ˆ
  51. Hydroxycitric acid ๐Ÿ›ˆ
  52. Indole-3-Carbinol ๐Ÿ›ˆ
  53. IP6 ๐Ÿ›ˆ 
  54. Iodine ๐Ÿ›ˆ
  55. Jiaogulan ๐Ÿ›ˆ
  56. Juglone ๐Ÿ›ˆ
  57. Laetrile ๐Ÿ›ˆ
  58. Larch arabinogalactan ๐Ÿ›ˆ
  59. Lipoic Acid ๐Ÿ›ˆ 
  60. Luteolin ๐Ÿ›ˆ
  61. Lycopene ๐Ÿ›ˆ 
  62. Mannose ๐Ÿ›ˆ
  63. Melatonin ๐Ÿ›ˆ
  64. Mistletoe ๐Ÿ›ˆ
  65. Moringa ๐Ÿ›ˆ 
  66. MSM ๐Ÿ›ˆ
  67. Myricetin ๐Ÿ›ˆ
  68. Naringin ๐Ÿ›ˆ
  69. Nattokinase ๐Ÿ›ˆ 
  70. Oil of Oregano ๐Ÿ›ˆ 
  71. Oleanolic acid  ๐Ÿ›ˆ
  72. Olive Leave Extract ๐Ÿ›ˆ
  73. Paeoniflorin ๐Ÿ›ˆ
  74. Panax Ginseng ๐Ÿ›ˆ
  75. Pau D'Arco ๐Ÿ›ˆ
  76. Piperlongumine ๐Ÿ›ˆ
  77. PQQ ๐Ÿ›ˆ
  78. Pterostilbene ๐Ÿ›ˆ 
  79. Quercetin ๐Ÿ›ˆ
  80. Reishi ๐Ÿ›ˆ 
  81. Resolvins ๐Ÿ›ˆ
  82. Resveratrol ๐Ÿ›ˆ
  83. Rosmarinic acid ๐Ÿ›ˆ
  84. Rutin ๐Ÿ›ˆ
  85. Ruta Graveolens ๐Ÿ›ˆ
  86. Sanguinarine ๐Ÿ›ˆ
  87. Scutellaria Baicalensis ๐Ÿ›ˆ
  88. Sea cucumber ๐Ÿ›ˆ
  89. Shikonin ๐Ÿ›ˆ
  90. Silibinin ๐Ÿ›ˆ
  91. Sulforaphane ๐Ÿ›ˆ
  92. Taurine ๐Ÿ›ˆ
  93. Theobromine ๐Ÿ›ˆ
  94. Tinospora cordifolia ๐Ÿ›ˆ 
  95. Triphala ๐Ÿ›ˆ
  96. Tripterygium wilfordii ๐Ÿ›ˆ
  97. Ursolic Acid ๐Ÿ›ˆ 
  98. Vitamin C ๐Ÿ›ˆ
  99. Vitamin D ๐Ÿ›ˆ
  100. Xylo-oligosaccharide ๐Ÿ›ˆ
  101. Zeolite ๐Ÿ›ˆ

Special Formula Supplements

  • Avemar ๐Ÿ›ˆ
  • Biobran MGN-3 ๐Ÿ›ˆ
  • Synergy Combination EpiQuercican™ Intensive ๐Ÿ›ˆ
  • Ukrain ๐Ÿ›ˆ
  • Peptides L-Canaline, ... ๐Ÿ›ˆ

    Never before did we have access to such a wide variety of supplements and natural products that can help beat cancer. Many of these natural products are inexpensive and most have little or no known toxicity at the recommended dosages. 

    There's no single natural cancer cure but there are many natural remedies that, combined with standard medical care, can help you manage and improve your odds of reversing cancer.



    The anticancer potential of the nutritional supplements listed here has been established either by laboratory and/ or animal studies, very few controlled human studies are done on nutritional supplements.

    Wednesday, August 1, 2018

    20 Anti-cancer Supplements Infographic



    Bovine Tracheal Cartilage
    Artemisinin
    Berberine
    Honokiol
    EGCG (Epigallocatechin Gallate)
    Jiaogulan
    Ursolic Acid
    Citric Acid
    Melatonin
    Turkey Tail
    Oleanolic Acid
    Panax Ginseng
    Salvia Miltiorrhiza
    C-phycocyanin
    D-limonene
    Luteolin
    Fucoidan
    Pyrroloquinoline (PQQ)
    Piperlongumine

    Note: I made this infographic in 2018 when my blog was still at anticancersupplements.blogspot. I moved to this blog since.

    Saturday, June 9, 2018

    Theory of Cancer

    According to the prevailing accepted theory of carcinogenesis {ref}, the somatic mutation theory, cancer arises when cells acquire many genetic mutations that promote abnormal growth and behavior. These mutations are believed to be the main factors responsible for converting normal cells into cancerous ones.

    But recent research is increasingly scrutinizing this mutation-focused viewpoint. New studies suggest that accumulating mutations alone do not fully explain the complex process of carcinogenesis. Instead, it is increasingly evident that mutagenesis can influence a range of biological processes, including epigenetic modifications, metabolic shifts, and alterations in the tumor microenvironment, thereby initiating and facilitating cancer development. Here's my thesis:

    Life’s ancient adaptations, buried deep in our genes, resurface under stress


    A fundamental characteristic of cancer cells is their inclination toward anaerobic respiration leading to the conversion of glucose into lactic acid instead of carbon dioxide {ref}. This is known as the Warburg Effect.

    Elevated lactic acid and inflammation promote each other in a malicious cycle {ref}. The onset and progression of inflammation can be triggered by a variety of factors: chronic stressors that may have contributed to the development of cancer {ref|ref|ref|ref|ref|ref|ref}, the tumor itself, the body’s response to the tumor, or cancer treatments (surgery, RX, chemotherapy). Additionally, dietary, lifestyle and environmental factors are contributing factors. 

    Incessant inflammation results in increased expression of HIF1ฮฑ {ref|refwhich further stimulates the glycolytic process, causing the production of more lactate contributing to persistent and increasing sub-toxic ammonia levels.

    Before the Great Oxygenation Event (GOE), the atmosphere contained very little oxygen. Instead, it had high levels of ammonia {ref}, which served as a crucial energy source for single-celled organisms like bacteria and yeast.

    Cancer cells tend to thrive in environments low in oxygen, which resemble the anaerobic environment of Earth before the GOE. Under these conditions, ammonia acts as a signaling molecule that triggers cellular growth and division {ref}. An increase in the amount of ammonia in tissues and a decrease in the ability of the body to excrete it raises lactic acid and interferes with oxygen uptake {ref}. This, in turn, leads to hypoxia and produces a shift towards glycolysis, perpetuating the deadly cycle

    Therefore, I propose that cancer is a metabolic disruption, and ammonia is both a catalyst and an energy source.
     
    The catalyst-like role of ammonia in cancer 



    —❖—

    The conventional theory of cancer: a genetic disease


    Cancer cells have gene mutations and will unceasingly continue to replicate. Gene mutations can be either inherited or acquired.

    DNA
    Examples of inherited mutations:
    • Hereditary breast-ovarian cancer syndrome
    • Lynch Syndrome
    • Li-Fraumeni syndrome
    • Cowden syndrome
    Acquired: dysregulation of more than 700 genes at multiple steps in cell signaling pathways.

    Cancer beyond the traditional genetic framework


    Metabolic, evolutionary, environmental, and even psychological factors that might contribute to cancer development.


    Cancer, a metabolic disease


    Can cancer metabolism be targeted to stop cancer proliferation?

    Toxic accelerated aging
    According to San-Millรกn and Brooks GA "Lactate is probably the only metabolic compound involved and necessary in all main sequela for carcinogenesis, specifically: angiogenesis, immune escape, cell migration, metastasis, and self-sufficient metabolism. We hypothesize that lactogenesis for carcinogenesis is the explanation and purpose of the Warburg Effect. Accordingly, therapies to limit lactate exchange and signaling within and among cancer cells should be priorities for discovery".

    "Warburg, Koch, and Szent-Gyorgyi had a comprehensive view of biology, in which the aerobic production of lactate, resulting from a respiratory defect, itself was functionally related to the nature of cancer." - Ray Peat, Ph.D. (1936-2022).

    Cancer, an evolutionary throwback (atavistic reversion theory)


    Cancer tumors are able to survive with very little oxygen, this supports the idea that cancer emerged when the amount of oxygen in the atmosphere was extremely low when life first appeared on our planet.

    Suggested treatments:
    • Increase oxygen in the body
    • Focus on the immune system, help trigger the patient's own immune system cells to attack cancer
    If cancer is part of the history of the cell and for whatever reason the cell reverted to that ancient function, trying to forever halt cancer via metabolic pathways as mentioned above, seems to be a near-impossible task to accomplish since many cancer cells will survive the most inhospitable and nutrient-deficient conditions.

    As for the reason, could it be that a normal cell becomes cancerous because of adaptation? Is the cell trying to adapt or cope with a changing habitat, e.g., less oxygen and more lactic acid? So the cell activates genes that a billion years ago were an efficient mechanism to deal with such an environment.



    Theory of Cancer Stem Cells (CSC)


    The cancer stem cell hypothesis proposes that tumors are comprised of a heterogeneous cell population, with only a subset of cells being responsible for the initiation, maintenance and progression of the disease. This subset of cells, referred to as cancer stem cells (CSCs), are thought to be responsible for the aggressiveness of tumors and may be resistant to chemotherapy and radiation. CSCs are believed to possess several key characteristics, such as self-renewal, tumor-initiating ability and the ability to differentiate into other cancer cell types.



    Cancer is a wound that does not heal.


    Chronic irritation theory. {Ref}


    Dr. John Prudden’s 31 Cases: Treating Cancer with Bovine Tracheal Cartilage. "Dr. John F. Prudden (1920-1998), found that bovine tracheal cartilage had a powerful and consistently positive effect on wound healing, arthritis, cancer, and other diseases."



    Melancholy as a risk factor for cancer



    Depression and the Immune System: A Close Connection {Ref}



    Cancer is caused by nutritional deficiencies.


    This thesis challenges the prevailing understanding of breast cancer causation by proposing that it may primarily be a deficiency disease, caused by the lack of a specific protective agent found in varying amounts in food, and ultimately, soil. {ref}



    Cancer cells that arise from bacteria


    BOCC hypothesis {Ref}   It's the Terrain

    Evidence supporting this hypothesis

    1. There are 10× more bacterial cells than human cells in the human body.
    2. Bacteria play a key role in carcinogenesis. 
    3. Like bacteria and single-celled eukaryotes (protists, e.g., yeast), cancer cells can grow in agar medium and form colonies, proliferate in the absence of anchorage in vitro, and ferment glucose in the absence of oxygen (anaerobic fermentation) with the production of lactic acid.
    4. Cancer cell genomes were assembled from DNA fragments all at once in a single catastrophic event (chromothripsis).
    5. Cancer cell genomes contain bacterial DNA.
    6. Genes of ancient and unicellular origin are highly and preferentially expressed during tumorigenesis.


    Cancer is a consequence of an acidic body and lymphatic obstruction.




    Cancer is a delayed severe hypersensitivity reaction.


    Reviewing a large body of evidence on many chronic inflammatory diseases and carcinogenesis the author proposes that cancer is a severe form of hypersensitivity responses (immune disorder) in site-specific tissues resulting from the accumulation of exaggerated expression and co-expression of immune responses and the creation of a molecular immune tsunami, primarily in the immune-responsive tissues. {ref}


    Cancer is first of all a cachexia accompanied by a tumor.


    It is proposed here that carcinogens deplete a vital substance and induce a metabolic deficiency that ends in cachexia. To survive, the organism grows a protective organ-the tumor-that replenishes the missing substance. {Ref}      


    Cancer is caused by a loss of efficient use of oxygen.


    Oxygen-Starved Tumor Cells Have Survival Advantage That Promotes Cancer Spread {ref}

    Stem-like cancer cells grow more rapidly under hypoxic conditions {study}

    {ref/ref}


    Dysregulation of the urea cycle


    Cancerous tumors disrupt the urea cycle, a process in the liver that breaks down nitrogen waste. This disruption allows tumors to hoard nitrogen, a crucial building block for DNA and RNA, thus fueling tumor growth. {ref}


    Cancer is the result of a homeostatic imbalance.


    About the intricate relationship between the body's natural state of equilibrium (homeostasis) and the development of tumors and their subsequent spread (metastasis). It emphasizes that cancer is not simply uncontrolled cell growth, but rather a breakdown in the delicate balance between cell growth and cell death.
    {ref}


    Cancer is caused by sulfate deficiency.


    The author claims that sulfate deficiency is a critical driver of various health issues, including cancer. She emphasizes the crucial role of sulfate in numerous bodily functions, particularly in the vasculature and cell function. She proposes that tumors, rather than being inherently harmful, actively work to alleviate the problems caused by sulfate deficiency.  {ref}  


    The Cell Competition Theory of Cancer


    This thesis proposes that cell competition plays a crucial role in both promoting and suppressing tumor formation. They show how mutations in YAP, KRAS or Pten can elevate cell fitness, and therefore, tumor cells harboring these mutations (winner) can outcompete wild-type parenchyma (loser). Inducing these mutations in the liver parenchyma is sufficient to trigger the opposite situation; cancer cells (loser) are eliminated by liver parenchyma (winner). {ref}


    —❖—