Our Magnetic Polarity Our Cadherins Our Phosphodiester Bonds Our Electrodynamic Light Medium And Presynaptic Neuron Compound Nitric Oxide

Our Phosphodiester Bonds Are Vital To All Life On Earth, As For, Bonds Of The Two Hydroxyl Groups In Phosphoric Acid "React" With Hydroxyl Groups On Other Molecules That Form Ester Bonds, As Our, Foundational Backbone Of Our Strands Of "Nucleic Acid". Our Phosphoric Acid Is Made From Our Mineral Phosphorus. Our Phosphorus Is An Essential Plant Nutrient That Is Taken Up By Our Plant Roots. Our Phosphates Generated In "Space", As, Phosphorus Oxoacids, An Acid That Contains Oxygen,That Were Carried By Meteorites And Comets. Our Phosphine Chemical Is Found In Our Interstellar Gas Clouds And In The Atmospheres Of Jupiter And Saturn And In The "Gas Jet" Of The Comet 67P. Our Phosphoric Acid Is A White "Crystalline" Solid Substance. Our Cancer Cells Tend To Lose Phosphorus Faster Than Normal Cells. Our Bones Contain The Bulk Of Our Phosphate. Our Cell Membranes Contain Phosphate As Part Of Their Structure. Our Phosphorus Is Our Nonmetallic Chemical Element Of Our Nitrogen Family And Is Made When Bound To Oxygen, As In, 4 Oxygen Atoms. Phosphorus And Calcium Are Vital To Our Health. Telomerase Is Not Always Found In Cancer Cells. Our Telomerase Is Our Ribonucleoprotein DNA Polymerase Complex That Maintains Telomere Length. When Telomerase Is Not Present Our Telomeres Shorten. Our Telomeres Are Our Segment DNA That Occurs At The Ends Of Our Chromosomes. These Are Our "Caps", As For, To Keep Our Chromosomes From Fusing Together. The Length Of Our Telomeres "Influences" The "Stability" Of Our Genetic Information. Cancer Is A Genetic Dis-ease, As For, Genetic Instability Is Prevalent In Most Cancers, As For, Genomic Instability Is From "Mutations" In Our DNA Repair Genes That Proliferates Cancer. There Is Isolation Of Phosphate Esters From Tumors. Metabolism Of Sugars, Might Contribute In Ribose Formation, As For, Ribose Is Vital To Our Nucleotides And Nucleic Acids, As For, This Ester Might Be Present In Tumors. Ribose Was Detected On Interstellar Ice Grains. Our Ribose Is A Sugar That Occurs In Our "Nature", As Our, Constituent Of Nucleosides, As Without A Phosphate Group, Vitamins And "Enzymes". There Are Low Levels Of Enzymes In Cancer. Our Phosphates Are For Our Phospholipids That Make-Up Our Cell Membranes. Our Phosphate Group Is Attached To A Carbon Molecule. Phospholipids Form A Bilayer Structure Of All Our Cell Membranes. Cancer Cells Exhibit An Increase In Phospholipid Content. Lipids Are Insoluable In Water And Have "Unique Geometry" That Causes Them To Cluster Into Bilayers Without Any Energy Input, As For, They Are Two-Faced Molecules With Water-Loving "Phosphate Heads And Water-Fearing Hydrocarbon Tails Of "Fatty Acids", As For, The "Polar Heads" And "Nonpolar Tails" Cause Our Phospholipids To Arrange Themselves In Layers. Our Phospholipid Molecule's "Polar Head" Is A "Phosphate Group". Our Polar Is Our Having Electrical Or Magnetic Polarity, In Which, Is Our "Geometry Of Atoms" In Our Molecules, As For, Polar Is Having Electrical Poles. Our Cell Polarity Mechanism Is Responsible For Our Cell's Shapes, As Well As, Regulation Of "Asymmetrical Cell Division", As For, Disturbance, As In, Disruption Of Cell Polarity Is Cancer. Curcumin And It's "Chalcone Parts" Inhibit The Growth Of Human Cancer Cells. Our Chalcone Is A "Yellow Crystalline" Ketone. If Our Body Lacks Glucose It Produces Ketones For Energy. Excess Lactate Production Compensates For ATP Production Defects That Is Caused By Dysfunctional Mitochondrial Oxidative Phosphorylation. Ketogenic Diets Starve Tumors By Issuing Fat And Protein, As For, Could Not Be Used By Glucose Dependent Tumor Cells. Genome Instability Is A High Frequency Of Mutations Within A Genome Of A Cell Lineage. Our Mutations Are "Alterations" In Our DNA Sequences, As Our, "Changes" In The Structure Of Our Genes. Our Alterations Are Our Adjustment Change Of Adaptation Of Modification, As In, Variation Of Conversion Or Revision. Our Gene Expression Involves Our "Regulator Gene", As For, This Code Forms A Repressor Protein. Our Cells Translate As Messenger RNA (mRNA) Are Decoded In Our Ribosome Decoding Center. Our Gene Expression Dictates The Structure And Function Of A Cell By Determining Which Proteins Are Made. A Protein, Cadherin-22 Is A Factor In Cancer Metastasis. Cadherins Are Calcium Dependent Adhesions, As A, Cell Adhesion Molecule. Cadherins Are Transmembrane Proteins That Are Dependent On Calcium Ions To Function. If Calcium Is Removed Adhesive Activity Is Nonexistant. Cadherins Molecules Act As Both Receptor And Ligand. Our Central Nervous System And Immune System Are Our Complexities And Our Cadherins May Relate To Our Central Nervous System. Our Cadherin Genes Are Involved In Our Cell-Cell Adhension Morphogenesis, Cell Recognition And Our Cell Signaling. Our Cell-Cell Adhesion Receptor, E-Cadherins Is An Important Factor Of Tumor Progression. There Is "Expression Patterns" Of Cadherin-Based Adhesion In The Morphogenesis And The Beginnings Of Functional Connections In The Central Nervous System. Neural Related Factors, That Are Important Constituents In The Development And The Activity Of Our Nervous System Have Been Found In Cancer Cells. Nerve Fibers Are Irregularly Found In Tumor Cells, Their Terminal's Interaction With Cancer Cells Are Neuro-Neoplastic Synapses. There Is A Direct Connection Between The Nervous System And Cancer Cells, As For, Chronic Stress Links Cancer Progression. There Are Specific Signaling Pathways That Impact Cancer Growth And Metastasis. Cancer Metastasis Depends On Many Interactions Between Metastatic Cells And Homeostatic Mechanism. Our Mechanisms For Our Homeostasis Are Our Temperature, Body Fluids, Blood, Sugar, Gas Concentrations, As In, Potential Of Hydrogen And Our Blood Pressure. In Our Highest Brain Potentiality, Referencing Our Luminous Ether, As In, Our "Light Bearing", As Our, Wave-Based Light To Propagate Through Empty Space, As For, Waves Should Not Be Able To Do. In Our Higher Brain Activity, There Is Our Concept Of Our Phenomena Of Electrodynamics, As For, Absolute Rest Electrodynamics And Optics, Meaning, Our Brain Activity While We Are "Resting", As In, "Calm" Is The Same As When Completing A Mental Task, The Task Is Performed More Efficiently, As For, This Incorporates Our Adaptations Of Our Neurons In Our Brain During Our Learning Process. Our Synaptic Plasticity Is Where An Increase In Synaptic Efficacy Arises From Our Presynaptic Cells Repeated And Persistant "Stimulation" Of The Post Synaptic Neurons. This Induces Lasting Cellular Changes That Add "Stability" And "Firing Efficacy" Is Increased And Is The Basis Of Our "Unsupervised Learning". This Is Our Activation Of Our Neighboring Neurons, As Well As, Retrograde Signaling To Modify Presynaptic Neuron Compound "Nitric Oxide". At Very High Temperatures Oxygen And Nitrogen Combine And Form Nitric Oxide. Our Nitric Oxide Can Change Our Computing Ability In Our Brain. Nitric Oxide Is Produced By Bacteria In Our Soil And In Our Oceans. Our Nitric Oxide Is Important For Our Human "Vasodilation", In Which, Relaxes The Inner Muscles Of Our Blood Vessels. Nitric Oxide Allows Our Blood, Our Nutrients And Our Oxygen To Travel Through Our Body. Thank-you.