Biochemist Dennis Hill interview; Cannabis oil as a cure for cancer

Background; Dennis Hill is a biochemist who graduated from the University of Houston Texas, doing his Graduate Work at Baylor Medical School.Employed as a researcher at the renowned MD Anderson Cancer Center in Houston Texas.
Five years ago Dennis was diagnosed with aggressive stage 3 prostate cancer, Thanks to cannabis oil he is now cancer free.
In the following video interview by Natalie Mazurek (2nd year chemistry student UTS Sydney), Dennis explains in chemistry terms, how the essential oil derived from cannabis kills cancer cells.
In the interview Dennis states “how it was trivial process using cannabis oil to cure himself of stage 3 prostate cancer.
No side effects, just a feeling of well being”
In this enlightening interview, Dennis explains in detail as only a biochemist could, how the cannabis works with the human bodies endocannabinoid system to kill cancer cells.

Interview by Natalie Mazurek, chemistry student UTS Sydney.

Interview glossary

Decarboxylation; (fundamental in the process of extracting cannabis oil)
Without this process the oil will not kill cancer cells!

Decarboxylation is a chemical reaction that removes a carboxyl group and releases carbon dioxide (CO2). Usually, decarboxylation refers to a reaction of carboxylic acids, removing a carbon atom from a carbon chain. The reverse process, which is the first chemical step in photosynthesis, is called carboxylation, the addition of CO2 to a compound. Enzymes that catalyze decarboxylations are called decarboxylases or, the more formal term, carboxy-lyases (EC number 4.1.1).

In organic chemistry
The term “decarboxylation” literally means removal of the COOH (carboxyl group) and its replacement with a proton. The term simply relates the state of the reactant and product. Decarboxylation is one of the oldest organic reactions, since it often entails simple pyrolysis, and volatile products distill from the reactor. Heating is required because the reaction is less favorable at low temperatures. Yields are highly sensitive to conditions. In retrosynthesis, decarboxylation reactions can be considered the opposite of homologation reactions, in that the chain length becomes one carbon shorter. Metals, especially copper compounds,[1] are usually required. Such reactions proceed via the intermediacy of metal carboxylate complexes.


endocannabinoid system;
The endocannabinoid system is a group of neuromodulatory lipids and their receptors in

the brain that are involved in a variety of physiological processes including

appetite, pain-sensation, mood, and memory; it mediates the psychoactive effects of

cannabis and, broadly speaking, includes:

The endogenous arachidonate-based lipids, anandamide (N-arachidonoylethanolamide,

AEA) and 2-arachidonoylglycerol (2-AG); these are known as “endocannabinoids” and are

physiological ligands for the cannabinoid receptors. Endocannabinoids are all

The enzymes that synthesize and degrade the endocannabinoids, such as fatty acid

amide hydrolase or monoacylglycerol lipase.
The cannabinoid receptors CB1 and CB2, two G protein-coupled receptors that are

located in the central and peripheral nervous systems.


In biochemistry and pharmacology, a ligand is a substance that forms a complex with a

biomolecule to serve a biological purpose. In protein-ligand binding, the ligand is

usually a signal-triggering molecule, binding to a site on a target protein. In DNA-

ligand binding studies, the ligand can be a small molecule, ion,[1] or protein[2] that

binds to the DNA double helix.


In biochemistry and pharmacology, a receptor is a protein molecule usually found

embedded within the plasma membrane surface of a cell that receives chemical signals

from outside the cell. When such chemical signals bind to a receptor, they cause some

form of cellular/tissue response, e.g. a change in the electrical activity of the

cell. In this sense, a receptor is a protein molecule that recognises and responds to

endogenous chemical signals, e.g. the acetylcholine receptor recognizes and responds

to its endogenous ligand, acetylcholine. However sometimes in pharmacology, the term

is also used to include other proteins that are drug targets, such as enzymes,

transporters and ion channels.

mimetic medicine;
Mimesis (/maɪˈmiːsəs/; Ancient Greek: μίμησις (mīmēsis), from μιμεῖσθαι (mīmeisthai),

“to imitate,” from μῖμος (mimos), “imitator, actor”) is a critical and philosophical

term that carries a wide range of meanings, which include imitation, representation,

mimicry, imitatio, receptivity, nonsensuous similarity, the act of resembling, the act

of expression, and the presentation of the self.[1]

In ancient Greece, mimesis was an idea that governed the creation of works of art, in

particular, with correspondence to the physical world understood as a model for

beauty, truth, and the good. Plato contrasted mimesis, or imitation, with diegesis, or

narrative. After Plato, the meaning of mimesis eventually shifted toward a

specifically literary function in ancient Greek society, and its use has changed and

been reinterpreted many times since then.


relating to, characterized by, or exhibiting mimicry

Tetrahydrocannabinol (THC), or more precisely its main isomer (−)-trans-Δ9-

tetrahydrocannabinol ( (6aR,10aR)-delta-9-tetrahydrocannabinol), is the principal

psychoactive constituent (or cannabinoid) of cannabis. First isolated in 1964 by

Israeli scientists Prof. Raphael Mechoulam and Dr. Yechiel Gaoni at the Weizmann

Institute of Science[8][9][10] it is a water-clear glassy solid when cold, which

becomes viscous and sticky if warmed. A pharmaceutical formulation of (−)-trans-Δ9-

tetrahydrocannabinol, known by its INN dronabinol, is available by prescription in the

U.S. and Canada under the brand name Marinol. An aromatic terpenoid, THC has a very

low solubility in water, but good solubility in most organic solvents, specifically

lipids and alcohols.[6] THC, CBD, CBN, CBC, CBG and about 80 other molecules make up

the phytocannabinoid family.


cbd (cannabidiol)
Cannabidiol (CBD) is one of at least 85 active cannabinoids identified in cannabis.[4]

It is a major phytocannabinoid, accounting for up to 40% of the plant’s extract.[5]

CBD is considered to have a wider scope of medical applications than

tetrahydrocannabinol (THC).[5] An orally-administered liquid containing CBD has

received orphan drug status in the US, for use as a treatment for Dravet syndrome,

under the brand name Epidiolex.[6]


Endogenous( made within the body)
Endogenous substances are those that originate from within an organism, tissue, or


Endogenous viral elements (EVEs) are DNA sequences derived from viruses that are

ancestrally inserted into the genomes of germ cells. These sequences, which may be

fragments of viruses, or entire viral genomes (proviruses), can persist in the

germline, being passed on from one generation to the next as host alleles.

Endogenous processes include senescence, the menstrual cycle and the self-sustained

circadian rhythms of plants and animals.

In some biological systems, endogeneity refers to the recipient of DNA (usually in

prokaryotes). However, because of homeostasis, discerning between internal and

external influences is often difficult.

Endogenous transcription factors refers to those that are manufactured by the cell, as

opposed to cloned transcription factors.

Exogenous ( outside of the body , ex plants)

In biology, an exogenous contrast agent in medical imaging for example, is a liquid

injected into the patient intravenously that enhances visibility of a pathology, such

as a tumor. An exogenous factor is any material that is present and active in an

individual organism or living cell but that originated outside of that organism, as

opposed to an endogenous factor.

Exogenous factors in medicine include both pathogens and therapeutics.
DNA introduced to cells via transfection or viral infection (transduction) is an

exogenous factor.
Carcinogens are exogenous factors.


Biomimetics or biomimicry is the imitation of the models, systems, and elements of

nature for the purpose of solving complex human problems.[1] The terms biomimetics and

biomimicry come from Ancient Greek: βίος (bios), life, and μίμησις (mīmēsis),

imitation, from μιμεῖσθαι (mīmeisthai), to imitate, from μῖμος (mimos), actor. A

closely related field is bionics.[2]


Anandamide, also known as N-arachidonoylethanolamine or AEA, is an endogenous

cannabinoid neurotransmitter. The name is taken from the Sanskrit word (and Hinduistic

religious term) ananda, which means “joy, bliss, delight”, and amide.[1][2] It is

synthesized from N-arachidonoyl phosphatidylethanolamine by multiple pathways.[3] It

is degraded primarily by the fatty acid amide hydrolase (FAAH) enzyme, which converts

anandamide into ethanolamine and arachidonic acid. As such, inhibitors of FAAH lead to

elevated anandamide levels and are being pursued for therapeutic use.[4][5]


Cannabinoid receptors are part of the cannabinoid receptor system in the brain and are

involved in a variety of physiological processes including appetite, pain-sensation,

mood, and memory.

Cannabinoid receptors are of a class of cell membrane receptors under the G protein-

coupled receptor superfamily.[1][2][3] As is typical of G protein-coupled receptors,

the cannabinoid receptors contain seven transmembrane spanning domains.[4] Cannabinoid

receptors are activated by three major groups of ligands, endocannabinoids (produced

by the mammilary body), plant cannabinoids (such as Cannabidiol, produced by the

cannabis plant) and synthetic cannabinoids (such as HU-210). All of the

endocannabinoids and plant cannabinoids are lipophilic, such as fat soluble compounds.


Cannabinoids are a class of diverse chemical compounds that act on cannabinoid

receptors on cells that repress neurotransmitter release in the brain. Ligands for

these receptor proteins include the endocannabinoids (produced naturally in the body

by humans and animals),[1] the phytocannabinoids (found in cannabis and some other

plants), and synthetic cannabinoids (manufactured artificially). The most notable

cannabinoid is the phytocannabinoid tetrahydrocannabinol (THC), the primary

psychoactive compound of cannabis.[2][3] Cannabidiol (CBD) is another major

constituent of the plant.[4] There are at least 85 different cannabinoids isolated

from cannabis, exhibiting varied effects.[5]


Chemical Component 2HE;
Helium is a chemical element with symbol He and atomic number 2. It is a colorless,

odorless, tasteless, non-toxic, inert, monatomic gas that heads the noble gas group in

the periodic table. Its boiling and melting points are the lowest among all the

elements and it exists only as a gas except in extremely cold conditions.


signalling metabolites;
Metabolites are the intermediates and products of metabolism. The term metabolite is

usually restricted to small molecules. Metabolites have various functions, including

fuel, structure, signaling, stimulatory and inhibitory effects on enzymes, catalytic

activity of their own (usually as a cofactor to an enzyme), defense, and interactions

with other organisms (e.g. pigments, odorants, and pheromones). A primary metabolite

is directly involved in normal “growth”, development, and reproduction. Ethylene is an

example of a primary metabolite produced in large-scale by industrial microbiology. A

secondary metabolite is not directly involved in those processes, but usually has an

important ecological function. Examples include antibiotics and pigments such as

resins and terpenes etc.


Ceramides are a family of waxy lipid molecules. A ceramide is composed of sphingosine

and a fatty acid. Ceramides are found in high concentrations within the cell membrane

of cells. They are one of the component lipids that make up sphingomyelin, one of the

major lipids in the lipid bilayer. Contrary to previous assumptions that ceramides and

other sphingolipids found in cell membrane were purely structural elements, ceramide

can participate in a variety of cellular signaling: examples include regulating

differentiation, proliferation, and programmed cell death (PCD) of cells.



Phyto–cannabinoids, also known as cannabinoids or exo–cannabinoids, are differentiated

from endo-cannabinoids due to their production from enzymes in a plant opposed to

being manufactured in a human, or better yet, a mammal. Cannabinoids come in many

shapes and functions. Today, there are many known unique phytocannnabinoids and

synthetic cannabinoids. Laboratories, like Montana Biotech, are currently assisting in

cannabinoid testing. This service can help patients get the most from this ancient

plant, cannabis.


Peptides (from Gr. πεπτός, “digested”, derived from πέσσειν, “to digest”) are

naturally occurring biological molecules. They are short chains of amino acid monomers

linked by peptide (amide) bonds. The covalent chemical bonds are formed when the

carboxyl group of one amino acid reacts with the amino group of another. The shortest

peptides are dipeptides, consisting of 2 amino acids joined by a single peptide bond,

followed by tripeptides, tetrapeptides, etc. A polypeptide is a long, continuous, and

unbranched peptide chain. Hence, peptides fall under the broad chemical classes of

biological oligomers and polymers, alongside nucleic acids, oligosaccharides and

polysaccharides, etc.


Metastatic lesion
Metastasis, or metastatic disease, is the spread of a cancer or disease from one organ

or part to another not directly connected with it. The new occurrences of disease thus

generated are referred to as metastases /mə ˈtæs tə siːz/ (sometimes abbreviated

“mets”).[1][2] It was previously thought that only malignant tumor cells and

infections have the capacity to metastasize (also spelled metastasise); however, this

is being reconsidered due to new research.[3] Metastasis is a Greek word meaning

“displacement”, from μετά, meta, “next”, and στάσις, stasis, “placement”.


Carboxylation in biochemistry is a posttranslational modification of glutamate

residues, to γ-carboxyglutamate, in proteins. It occurs primarily in proteins involved

in the blood clotting cascade, specifically factors II, VII, IX, and X, protein C, and

protein S, and also in some bone proteins. This modification is required for these

proteins to function. Carboxylation occurs in the liver and is performed by γ-glutamyl


The carboxylase requires vitamin K as a cofactor and performs the reaction in a

processive manner.[5] γ-carboxyglutamate binds calcium, which is essential for its

activity.[6] For example, in prothrombin, calcium binding allows the protein to

associate with the plasma membrane in platelets, bringing it into close proximity with

the proteins that cleave prothrombin to active thrombin after injury.[7]


Adenosine triphosphate (ATP) is a nucleoside triphosphate used in cells as a coenzyme,

often called the “molecular unit of currency” of intracellular energy transfer.[1]

ATP transports chemical energy within cells for metabolism. It is one of the end

products of photophosphorylation, cellular respiration, and fermentation and used by

enzymes and structural proteins in many cellular processes, including biosynthetic

reactions, motility, and cell division.[2] One molecule of ATP contains three

phosphate groups, and it is produced by a wide variety of enzymes, including ATP

synthase, from adenosine diphosphate (ADP) or adenosine monophosphate (AMP) and

various phosphate group donors. Substrate-level phosphorylation, oxidative

phosphorylation in cellular respiration, and photophosphorylation in photosynthesis

are three major mechanisms of ATP biosynthesis.


mitochondrial (mt) membrane;
Mitochondrial membrane transport proteins are proteins which exist in the membranes of

mitochondria and which serve to transport[1] molecules and other factors such as ions

into or out of the organelles.

Endoplasmic reticulum;
The endoplasmic reticulum (ER) is a type of organelle in the cells of eukaryotic

organisms that forms an interconnected network of flattened, membrane-enclosed sacs or

tubes known as cisternae. The endoplasm is the inner core of the cytoplasm and the

membranes of the ER are continuous with the outer membrane of the nuclear envelope.

6 thoughts on “Biochemist Dennis Hill interview; Cannabis oil as a cure for cancer

  1. Did dennis get a bit mixed up when he said there are 60 enocannabinoids? I think he is confused with Phytocannabinoids which at least 60 have been identified. I’ve never heard any estimates of 60 endocannabinoiods in the human body.


  2. This information may be use full to some, but all we want to know is where and how do we get this life saving oil etc. I live in Canada and now they say its legal. Does this mean I won’t get arrested for trying to cure my Cancer? Is there a way to help people that have limited means (say pensioners) to be able to afford this cure or is it just for the wealthy?


    • Someone in Canada will hopefully see this and weigh in with details.

      It isn’t only for the rich. In the U.S., there are co-ops that provide the medicine to those in need at no cost. I know that wonderful people and miracles exist in Canada too, be open to that. Maybe say a prayer, and know that you will get the medicine you need.


  3. Oops, silly me. Of course there are not 60 endocannabinoids native to the body. My mistake, so please don’t quote me. I have heard that there are probably more than 60 phytocannabinoids. What a wonder of therapeutics. ~Dennis

    Liked by 1 person

  4. (It isn’t only for the rich. In the U.S., there are co-ops that provide the medicine to those in need at no cost. I know that wonderful people and miracles exist in Canada too, be open to that. Maybe say a prayer, and know that you will get the medicine you need.)I Thank you for your positive reply. Please let us here in Canada if there are places we can go to for this badly needed medicine. time is the only thing that we all pray for. To find this medicine before its too late for some of us. anxiously awaiting, Robert Ednie


    June 30, 2015

    Self-Described ‘Cannabis College’ Sprouts Offshoots as More States Legalize Marijuana
    30oaksterdamChronicle photo by Colleen Murphy
    A session at Oaksterdam U.’s seminar this past weekend in Washington. The university is not an accredited institution, but that has not stood in the way of its budding growth, among users, purveyors, and planters.

    By Colleen Murphy


    Oaksterdam University is not an accredited institution, but you might have been fooled if you went to the Capital Hilton here this past weekend.

    More than 100 students took part in a 10-session seminar, part of the cannabis college’s focus on education in regions with recently loosened marijuana laws. During one session on Sunday, an instructor flipped through PowerPoint slides about cannabis-extraction methods and wove organic chemistry into one presentation. Meanwhile, attendees — clad in Oaksterdam sweatshirts, tie-dyed T-shirts advertising the marijuana newspaper High Times, and marijuana-leaf tie-clips — dutifully took notes.

    Hanging in the ballroom were posters with the slogan “Cannabis freedom is closer than you think” and Oaksterdam’s marijuana-leaf-shaped crest, which looks something like Harvard University’s, except with “cannabis” replacing “veritas.”

    The university, which markets itself as a mix of a trade school and an advocacy group, opened in 2007, and it is booming. Students paid as much as $800 each to attend the sessions and an after party at a glitzy M Street restaurant here. Fourteen-week semesters at Oaksterdam’s flagship campus, in Oakland, Calif. — the source of its name in a mashup with pot-friendly Amsterdam — are booked six months ahead of time. Weekend seminars sell out two months in advance as

    Oaksterdam takes its “show on the road,” said Aseem Sappal, provost and dean of faculty at Oaksterdam.

    Attendees this weekend included dispensary owners, doctors, and recent college graduates, Mr. Sappal said. Sessions covered such topics as federal and state marijuana laws, the history of cannabis use, the economics of the industry, and cooking with cannabis.

    “It’s really important that you spread education because there’s way too much that people don’t realize,” Mr. Sappal said in an interview on Sunday. “You’re going to continue to pass laws, and all of a sudden you’re going to start a dispensary, which is great. But who’s going to teach you how to open that dispensary? Who’s going to teach you how to cultivate?”

    In its push to educate marijuana users, growers, and purveyors, Oaksterdam officials are considering opening a campus next year either here or in New York City. Las Vegas and Colorado are also contenders, Mr. Sappal said. Nearly two dozen states have now legalized marijuana, and Mr. Sappal argued that “it’s just a matter of time before the entire nation legalizes.”

    A Chance to Eliminate Stigma
    Vuth Chao, who installs what he calls marijuana gardens in homes here, said he had come to the session to brush up on his technical knowledge. He said he would probably take more Oaksterdam seminars in the future to continue building his network.

    He said he had so far installed three gardens — a process that involves interviewing customers to find out about their needs — and hoped to install more as he builds his reputation. Mr. Chao said that since marijuana was legalized in the city, in February, he has seen the culture around marijuana use become slightly friendlier, but there’s still a “gray area.”

    “If people don’t know me, they’re not going to let me go in their house and, like, set up cannabis,” Mr. Chao said. “It’s a comfort zone. We have to get over that as a society too.”

    Becoming more comfortable with marijuana should extend to college and university administrators too, argued Paul Zukerberg, a Washington-based lawyer who has represented students at American, George Washington, and Georgetown Universities in marijuana cases. Mr. Zukerberg led a Saturday session on the differences between state and federal marijuana laws.

    He said that although marijuana is now legal in Washington, D.C., local universities are “behind the times.”

    “They don’t, for example, allow medical marijuana in dorms,” Mr. Zukerberg said. “They continue to discipline students for marijuana use, even though it’s legal under the local law.”


Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s