CrossFit | Cancer and Metabolism, Part 2

Cancer and Metabolism, Part 2

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ByProfessor Richard FeinmanAugust 26, 2019

From previous CrossFit modules and general background, we’ve established:

  • Energy metabolism in most organisms proceeds in two major phases: Glycolysis oxidizes glucose to pyruvate (pyruvic acid) in an anaerobic process. Pyruvate can be oxidized to CO2 through the process of respiration in which molecular oxygen (O2) is the final oxidizing agent.
  • Note: The acid name of organic acids, e.g., pyruvic acid, is used interchangeably with its salt name, pyruvate. In biochemistry, we mostly study things at neutral pH, where pyretic acid exists almost entirely in the pyruvate form.
  • The Warburg effect provides a major focus: Many cells that in their normal state have a high aerobic metabolism switch to glycolysis in the cancerous state, even if oxygen is available. This activity in the presence of oxygen is sometimes referred to as “aerobic glycolysis” although the glycolysis itself is still anaerobic.
  • The oxidizing agent that converts glucose to pyruvate in glycolysis is the cofactor NAD+, which is itself reduced to NADH. Aerobic cells put the NADH into respiration, where it is re-oxidized back to NAD+ allowing another round of glycolysis. Cells that obtain energy only from glycolysis recycle the NADH by reducing pyruvate to lactate (lactic acid). This is what Warburg found: Cancer cells have a higher ratio of lactic acid to CO2 than normal cells. Looking ahead, this is a good step at which to look for a control point for the Warburg effect — the connection between aerobic and anaerobic processes.
  • Cells that carry out respiration convert pyruvate to acetyl-CoA. Acetyl-CoA is the substrate for respiration and is oxidized to CO2. In addition to pyruvate from glycolysis, metabolism provides other sources of acetyl-CoA, the largest of which are fatty acids from fat.
  • Acetyl-CoA can be supplied to peripheral tissues by the liver. To do this, the liver forms ketone bodies, beta-hydroxybutyrate, and acetoacetate. The ketone bodies are carried in the blood to other tissues where they are broken down again to supply acetyl-CoA. The liver itself does not use ketone bodies because it has its own acetyl-CoA
  • A big idea: The Warburg effect represents a disconnect between anaerobic metabolism and respiration — that is, about the connection between pyruvate and acetyl-CoA. In bypassing the link providing acetyl-CoA, ketone bodies present a way to dissect the process and possibly offer some help.

Figure 1

More on Energy Metabolism

Because of the need to maintain control and avoid the high temperatures that might be required for big chemical changes, biochemical processes generally proceed in many small steps. Respiration comprises two major components. The first is the so-called Krebs cycle, or tricarboxylic acid (TCA) cycle, in which acetyl-CoA is oxidized to CO2 by redox coenzymes, the main one, again, NAD+. The product, NADH, along with NADH from other processes like glycolysis, is funneled into a second process called the electron transport chain, a process vaguely analogous to electrical conduction, but at the end of the chain, at last, molecular oxygen is reduced to water.

Figure 2

The Mitochondrion

The functional phases of metabolism are separated in space as well as activity. The pill-shaped structure, the mitochondrion, is the site of oxidative processing. Two membranes enclose the interior space, which is called the matrix. The outer membrane is a barrier to certain substances, but it is the inner mitochondrial membrane that contains the machinery for metabolic processing. The inner membrane has high structure with extensive invaginations called cristae. The enzymes and proteins that carry out the final oxidations and generation of ATP are embedded in the inner membrane.

The importance of this cellular structure and the visible, morphological changes that accompany the cancerous state have encouraged us to look for extensive breakdown in the mitochondrion in understanding cancer. While there are some cancers with clearly disrupted mitochondria, the organelle is not generally smashed up, and in fact, many cancers have well-functioning mitochondria. We have to look for more subtle changes. In fact, lots of things can go wrong. Here’s one: Entry of pyruvate into the mitochondrion is disrupted in most cancers.

Figure 3

Pyruvate enters the mitochondrion through the MPC protein transporter that comprises two subunits called MPC1 and MPC2. Right off, there is potential for trouble. It turns out both subunits are required for normal oxidative metabolism, and most cancers show a reduced expression or absence of either or both of these carriers. Most often it’s MPC1. The identification of the genes controlling the MPC complex has allowed a test of what would happen if you could get the gene to re-express MPC and whether this would be beneficial. John Schell, et al. were able to modify cancer cells growing in culture to re-express both MPC1 and MPC2 (1). The modified cells showed reduced reliance on glycolysis and increased uptake of pyruvate into the mitochondrion compared to control tumors. In addition, when xenografts (from other animals) in mice were prepared, those grafts with re-expressed MPC1 and MPC2 shrank in size compared to the control tumor (Figure 4).

So, some cancers show the defect in the ability to get pyruvate into the mitochondrion. This has bearing on the possible molecular basis of the Warburg effect — i.e., the connection between glycolysis and respiration. It turns out that that is probably only part of the picture. Processing of the pyruvate that enters the mitochondria is where a lot of the action is. To understand this, we take a short digression on enzymes.

Figure 4

Background on Enzymes

All biochemical reactions are controlled by enzymes, which are proteins that perform as catalysts. A catalyst increases the rate of a chemical reaction and provides control. For reactions that are reversible, the enzyme will catalyze the reaction in both directions. It will only allow equilibrium to be attained faster.

The names of enzymes roughly tell you what reaction is catalyzed (although there are many old traditional names that are not always informative).

For example:

Alcohol dehydrogenase: ethanol + NAD+ ➛ NADH + acetaldehyde.
Aldehyde  dehydrogenase: acetaldehyde + NAD+ ➛ NADH + acetic acid.
Pyruvate dehydrogenase: pyruvate + coenzymeA + NAD+ ➛ NADH + acetyl-CoA + CO2.
Lactate dehydrogenase: pyruvate + NADH ➛  NAD+ + lactate.

Kinases and Phosphatases

Much of metabolism depends on regulation of enzymes by chemical modification. Of overwhelming importance are phosphorylation and dephosphorylation — i.e., the transfer and removal of phosphate units. The source of phosphate transferred to substrates is ATP, and the majority of enzymes that perform that function are called kinases. Enzymes that undo the effect of kinases, that catalyze the breakdown (hydrolysis) of phosphorylated compounds, are called phosphatases. If the substrate is a protein, the enzymes are referred to generically as protein kinases and protein phosphatases unless the particular protein is specified. Tyrosine kinases are protein kinase, which specifically modify the tyrosine residue within a protein (not free tyrosine).

Modern cell biology is about the spectrum of hundreds of kinases and phosphatases that keep the cell in a particular functional state. The term kinome is sometimes used to describe this array of enzymes and substrates.

Pyruvate Dehydrogenase: The Metabolic Traffic Cop

Pyruvate dehydrogenase (PDH) represents a key control point in energy metabolism. The immediate link between glycolysis and respiration, PDH catalyzes the transformation of pyruvate into acetyl-CoA, the substrate for the TCA cycle.

Figure 5

The overall oxidation of pyruvate to acetyl-CoA is as written above, but the reaction actually proceeds in three steps involving three different enzyme activities. The structure of PDH reflects the complex nature of the chemistry — there are multiple copies of each of the enzymes, and PDH is sometimes referred to as the pyruvate dehydrogenase complex (PDC). The three enzymes carry out the components of the reaction: 1) oxidative decarboxylation with attachment to lipoic acid coenzyme, 2) transfer of coenzyme A, releasing reduced lipoic acid, and re-oxidation of lipoic acid by flavin and NAD+.

If there is little glucose, pyruvate will be provided by the metabolism of protein and the conversion of amino acids into pyruvate or other substrates for gluconeogenesis. Under these conditions, most acetyl-CoA comes into the mitochondrion from fat, so this is the point at which fat and carbohydrate metabolism meet. Here, we are looking at the site of regulation for ketogenic diets. To understand PDH, we have to ask the question: On a low-carbohydrate or ketogenic diet, how does the mitochondrion know to turn any pyruvate into glucose rather than acetyl-CoA, and how does it know to use incoming fat for aerobic metabolism?

Figure 6

Acetyl-CoA, the product of the PDH reaction, regulates its own production. Strong negative feedback keeps the cell from turning pyruvate into acetyl-CoA if 1) there is already plenty of acetyl-CoA coming in from fat metabolism, and 2) there is no dietary carbohydrate coming in and the pyruvate needs to be used to provide glucose (gluconeogenesis). PDH is thus a branch point for metabolism and a reasonable place to look for how things might go awry in the oncogenic state.

Pyruvate Dehydrogenase in Cancer

Several cancers have, in fact, been associated with inhibition of PDH regulation.

T. McFate et al. identified inhibition of PDH in a human head and neck squamous cell carcinoma (cancers of cells in lining of internal organs)(2). The actual defect was over-expression of an enzyme that regulates PDH activity. We saw that PDH senses the amount of acetyl-CoA in the mitochondrion, and as that gets high, PDH activity is reduced. There is another level of regulation, however. PDH is an enzyme that is inhibited when modified by phosphorylation. The enzyme that catalyzes the phosphorylation, pyruvate dehydrogenase kinase-1 (PDK-1), is turned on by many things, including acetyl-CoA, ATP, and NADH (all the signals of already active oxidative metabolism). So acetyl-CoA not only inhibits PDH directly but also turns on an enzyme that will inhibit PDH by phosphorylation.

Figure 7

When the over-expression of PDK-1 in the carcinoma was knocked down, tumor growth and invasiveness were inhibited (2). The example is interesting from the perspective of the metabolic approach to cancer. It turns out that a protein known as HIF-1 (hypoxia-inducible factor) regulates PDK-1 and HIF-1, then is regulated by glycolytic intermediates, including lactate and pyruvate. This represents a positive feedback loop where inhibition of PDH by acetyl-CoA and PDK-1 prevents utilization of pyruvate in aerobic metabolism, and pyruvate itself makes the problem worse by further inhibition.

Oncogene Src as Inhibitor of PDH

The Rous sarcoma virus was discovered years before the Warburg effect. Peyton Rous showed that the causative agent in sarcoma was a virus, although it took many years for the viral effect to be accepted. The key gene was designated Src and was the first oncogene to be discovered. It was found that the gene coded for a tyrosine kinase. In 2016, Y. Jin et al. showed that one of the targets of this kinase was a tyrosine residue on PDH (3). This was found to be a different locus than the serine that is the site of phosphorylation by PDK-1. Jin et al. found that the Src kinase increased the production of ROS (reactive oxygen species). These reactive oxygen species are themselves capable of activating Src, producing a negative feedback loop that will further inhibit PDH. Figure 7 shows a summary of major control points of PDH activity.

Summary

The metabolic approach to cancer asks how the Warburg effect occurs, how the normal link between glycolysis and respiration becomes disturbed. Looking at one likely candidate, PDH, a regulator of the flow of pyruvate into oxidative metabolism, shows several different kinds of defects. Different cancers show impaired uptake of pyruvate into the mitochondrion and/or reduced activity of PDH by direct phosphorylation or over-expression of PDK-1. It remains to be discovered which of these provides control, how they interact, and whether any can be targeted for therapy.


Additional Reading


references

  1. Schell JC, et al. A role for the mitochondrial pyruvate carrier as a repressor of the Warburg effect and colon cancer cell growth. Molecular Cell 56(2014): 400–413. Available here.
  2. McFate T, et al. Pyruvate dehydrogenase complex activity controls metabolic and malignant phenotype in cancer cells. J. Biol Chem. 283.33(2008): 22700-8. Available here.
  3. Jin, Y. Src drives the Warburg effect and therapy resistance by inactivating pyruvate dehydrogenase through tyrosine-289 phosphorylation. Oncotarget 7(2016): 25113-25114.

Richard David Feinman, Ph.D., is a professor of cell biology at the State University of New York Downstate Medical Center in Brooklyn, where he has been a pioneer in incorporating nutrition into the biochemistry curriculum. A graduate of the University of Rochester and the University of Oregon, Dr. Feinman has published numerous scientific and popular papers. He is the founder and former co-editor-in-chief (2004–2009) of the journal Nutrition & Metabolism. He is currently researching the application of ketogenic diets to cancer.

Comments on Cancer and Metabolism, Part 2

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RAPHAEL SIRTOLI
September 3rd, 2019 at 8:51 am
Commented on: Cancer and Metabolism, Part 2

Thanks for the thoughtful answer Prof.


I do think Schurr is arguing against commonly held notions of glycolysis. For example, he quotes mainstream textbooks such as the 4th edition of ‘Biochemistry’ by Stryer (1995), and the 7th edition ‘Biochemistry’ (Berg et al., 2012) before countering their claims.

You, Schurr and I agree that “The flow of pyruvate is determined by what else is going on and what else is there (NAD+, ATP, etc.)” but may disagree as to where in the glycolytic path this happens.


We would argue that it’s thermodynamically favorable to end up with lactate starting with glucose, and that depending on NAD/NADH, ATP/ADP ratios, O2 concentrations and the particular cell type, the lactate will or won’t get converted to pyruvate. If it is, then mitochondrial LDH can turn it into pyruvate for mitochondrial oxidative metabolism (e.g. for cerebral energy production via the lactate-shuttle hypothesis). If it not, then as you say it may be exported to the liver. Cerebral oxidative metabolism with lactate is an important point, as it demonstrates the ability of lactate to be a primary oxidative substrate in certain cell types. This is serves as a notable exception to:


Glucose + 2ATP + 4ADP + 2Pi + 2NAD+ ==> + 2pyruvate + 2ADP + 4ATP + 2NADH




From another of Schurr’s papers, here’s the argument for glycolysis to lactate making more sense thermodynamically (https://www.ncbi.nlm.nih.gov/pubmed/15973352):




“Thermodynamically, glycolysis should proceed to completion, that is, lactate formation, since pyruvate conversion to lactate yields free energy (deltaG^0' =-6 kcal/mol). Chemically, glycolysis should proceed to form lactate, since the LDH reaction regenerates nicotinamide adenine dinucleotide (NAD+) by oxidizing its reduced form (NADH) formed during the glyceraldehyde phosphate (GAP) dehydrogenase reaction and thus assuring the cyclical nature of glycolysis […] Furthermore, the assumption that under aerobic conditions pyruvate conversion to acetyl-SCoA, a reaction that takes place in the mitochondrion and requires NAD+, is somehow thermodynamically

preferable over pyruvate conversion to lactate is unsubstantiated. This assumption would have some basis if the glycolytic enzymes, substrates and products were, as was believed for many years, floating freely in a cytosol that behaves like an aqueous medium”


I would very much like to hear your comments once you’ve read the paper in detail, as i think you will appreciate the historical perspective it takes (if for nothing else).


Thanks for your stimulating comments

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Mike Numon
August 27th, 2019 at 2:06 pm
Commented on: Cancer and Metabolism, Part 2

Great article! I love reading about this. It got me thinking though, has any of the research looked at concentrations of NAD+ and it's relationship to cancer? Also, what about glutamine knock-out as an inhibitor for cancer metabolism, how does that play a role, relatively to the ketogenic diet?

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Richard Feinman
August 28th, 2019 at 2:01 am

These are important topics for whole new stories. I will try to consider some in future posts and/or point you to relevant papers.

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RAPHAEL SIRTOLI
August 27th, 2019 at 9:51 am
Commented on: Cancer and Metabolism, Part 2

Hi Prof,


Great series on cancer. I'd like to challenge you on your statement: "Glycolysis oxidizes glucose to pyruvate (pyruvic acid) in an anaerobic process." The reason is that a better model of glycolysis may better explain the efficacy of ketogenic metabolism in cancer.


Avital Schurr argues that glycolysis always ends in lactate, not pyruvate.


"Cerebral glycolysis: a century of persistent misunderstanding and misconception" http://www.ncbi.nlm.nih.gov/pubmed/25477776


A few points to stimulate your curiosity:


1) "No difference is known between the glycolytic apparatus of red blood cells and that of any other tissue and yet, erythrocyte glycolysis produces lactate in the presence of oxygen (or its absence), while glycolysis of any other oxygenated tissue supposedly produces mainly pyruvate"

2) "the existence of a functional LDH in the mitochondrial membrane negates the need for the MAS (Malate-Apartate Shuttle) as the mechanism responsible for transporting NAD+ into the mitochondrion from the cytosol" i.e. solves the NAD+ recycling issue


A summary quote

"it is of utmost importance to redefine 'glycolysis' as the cytosolic biochemical pathway that under both, aerobic and anaerobic conditions, constantly utilizes glucose as its initial substrate to produce lactate as its end product in cerebral tissue and in almost any other tissue. The NAD+ that is reduced to NADH during the formation of pyruvate is being reformed by the glycolytic LDH during the conversion of pyruvate to lactate, affording this portion of the pathway its cyclical nature. Under aerobic conditions lactate is utilized as the main substrate of the mitochondrial tricarboxylic acid (TCA) cycle, and thus, is defined as the major coupler between the two pathways"


I'm curious to hear your thoughts

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Richard Feinman
August 27th, 2019 at 7:23 pm

I have not read the paper in detail. It discusses many points but from the abstract and restricting discussion to the present case, the paper is not quite right, partly because it is arguing against ideas that are not held by most people. I think it is generally understood that lactate can function as a substrate for oxidative metabolism.


As stated, your summary quote beginning "it is of utmost importance..." is wrong. "Under aerobic conditions lactate is the main substrate..." is not true or more precisely is at best a sometime thing. The error seems to be that that the paper is considering a dynamic mechanism as if it were fixed. A metabolic map is like any map. It only tells you where the roads are.. It doesn't tell you whether the bridge collapsed in the last storm or whether they just finished expanding the road to four lanes. The flow of pyruvate is determined by what else is going on and what else is there (NAD+, ATP, etc.)


The point of part 2 is that PDH is the traffic cop. If there is high traffic (exercise), the cop in the muscle will point pyruvate to LDH and export the lactate through the off-ramp and road towards the liver. (I will try not to let the analogy get out of control). The cop in the liver will point the incoming lactate traffic into pyruvate and then into gluconeogenesis (NOT into energy metabolism. (I just described the Cori cycle, of course). As rush hour subsides (race is over) pyruvate will go into the TCA cycle but not via lactate. Lactate that appears from other sources will be oxidized. One of the problems in cancer is that the cop is not always there and not doing well when he is.


The evidence is experimental but it would make no sense energetically. Pyruvate + NADH --> lactate ) is downhill but so is pyruvate + NAD+ --> acetyl-CoA . The pathway pyruvate --> lactate --> pyruvate --> acetyl-CoA --> TCA cycle does not happen as a general mechanism, at least in the same place. (The Cori cycle, above separates that between liver and muscle).


Does this answer the question?

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