Nutraceutical composition and method of use for treatment / prevention of cancer

A method of inhibiting metastasis of cancer in a host, the method comprising administering to said host, a therapeutically effective amount of:

• (a) At least one herb selected from the group consisting of wild yam root (Dioscorea villosa), teasel root (Dipsacus asper), balm of gilead bud (Populus balsamifera), bakuchi seed (Cyamopsis psoralioides), dichroa root (Dichroa febrifuga), kochia seed (Kochia scoparia), kanta kari (Solanum xanthocarpum), bushy knotweed rhizome (Polygonum Cuspidatum), arjun (Terminalia arjuna), babul chall bark (Acacia Arabica), Sweet Myrrh (Opopanax) and bhumy amalaki (Phyllanthus nirur) and optionally at least one herb selected from the group consisting of Frankincense (Boswellia carteri), Garcinia Fruit (Garcinia cambogia), Vitex (Vitex agnus-castus), Dragons Blood (Calamus draco), Mace (Myristica fragans), White Sage (Salvia apian) and Red Sandalwood (Pterocarpus santalinu);
• and/or
• (b) 2-3-dimethoxy-5-methyl-1,4 benzoquinone and/or ubiquinones (5-45), wherein said 2-3-dimethoxy-5-methyl-1,4 benzoquinone and/or ubiquinones (5-45) further comprise chemical analogues and precursors;
• said analogs further comprising one or more of hydroquinones, ubichromenols (0-45), ubichromanols (0-45) and ubiquinols (0-45), said precursors further comprising one or more of para-hydroxybenzoate, para-hydroxycinnamate or para-hydroxyphenylpyruvate, para-hydroxyphenyllactate, poly-prenyl-para hydroxybenzoate, tyrosine, phenylalanine and isopentyl-diphosphate;
• and
• (c) at least one substance, capable of augmenting oxidative phosphorylation or mitochondrial respiration, herein termed “OXPHOS (+)”;
• wherein said OXPHOS (+) is selected from the group consisting of riboflavin, flavin mononucleotide, flavin adenine dinucleotide, 5-amino-6-(5′-phosphoribitylamino)uracil,6,7-Dimethyl-8-(1-D-ribityl)lumazine, ribitol, 5,6-dimethylbenzimidazole, pharmaceutically acceptable salts, precursors and derivatives of the vitamin B2 molecule, ubiquinone (50), tetrahydrobiopterin, vitamin B1, lipoic acid, biotin, vitamin B6, vitamin B12, folate, niacin, vitamin C and pantothenic acid;
• and/or
• (d) at least one substance that can inhibit lactic acid dehydrogenase herein termed “LDH (−)”;
• wherein said LDH (−) is selected from the group consisting of 2′,3,4′5,7-pentahydroxyflavone, epigallocatechin gallate, quercetin, citric acid, rosemary (Rosmarinus officinalis), black walnut (Juglans nigra), clove (Syzygium aromaticum), nutmeg (Myristica fragans), licorice root (Glycyrrhiza glabra), coriander (Coriandrum sativum), cinnamon (Cinnamomum cassia), ginger root (Zingiber officinale), Myrrh Gum (Commiphora molmol) and green tea (Camellia sinensis);
• and
• (e) optionally, at least one alkalizing agent selected from the group consisting of aloe vera (Aloe barbadensis), chlorella (Chlorella pyrendoidosa), wheat grass (Triticum aestivum), sodium or potassium bicarbonate and potassium;
• and/or
• (f) optionally, at least one antiproliferative herb selected from the group consisting of Speranskia Herb (Speranskia tuberculata) and Goldenseal (Hydrastis Canadensis);
• and/or
• (g) optionally, at least one herb selected from the Table 1 B-E;
• (h) optionally, one or more chemotherapy drug(s) used for the treatment of cancer and/or a pharmaceutically acceptable carrier.