Metabolic Adaptation of Cancer Cells Flashcards

1
Q

What is (18)F-FDG?

A

2-deoxy-2-(18)fluoro-D-glucose

  • Contains radioactive fluoride
  • Glucose can’t be further metabolised
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2
Q

Which cell type have a high capacity to take up (18)F-FDG?

A

Tumour cells

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3
Q

How does positron emission tomography (PET) detect tumour cells that have taken up (18)F-FDG?

A

Radioactive decay of fluoride releases gamma rays

Detected by PET

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4
Q

What is the Warburg effect?

A

Most cancer cells shift from ATP generation through oxidative phosphorylation to glycolysis, even under normal oxygen concentrations

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5
Q

What are the consequences of the Warburg effect?

A

Cancer cells derive most of their energy from aerobic glycolysis
Accumulate (18)F-FDG (and glucose)
Reduced rate of pyruvate metabolism in TCA cycle and oxidative phosphorylation

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6
Q

How does the lactate produced by cancer cells change the environment around it?

A

More acidic > may stimulate neovascularisation

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7
Q

How do cancer cells accumulate large amounts of glucose?

A

Hyperactivity of GLUT1

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8
Q

What is the major end point of glucose metabolism in cancer cells under aerobic conditions?

A

Glycolysis, making lactate

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9
Q

How is glycolysis re-engineered in cancer cells?

A
Over-expression of GLUT1
Glycolytic enzymes over-expressed
- Hexokinase
- PFK1
- Lactate dehydrogenase
Over-expression of pyruvate kinase M2 (PKM2)
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10
Q

What is PKM2?

A

Foetal isoform of pyruvate kinase with lower activity

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11
Q

Expression of which enzymes is induced by hypoxia in cancer cells, allowing them to do what?

A

Expression of
- Glycogen phosphorylase
- Glycogen synthase
Can store and use glycogen

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12
Q

In the early stage of tumour development, which cells in the mass are most hypoxic?

A

Those in centre

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13
Q

Why does (18)F-FDG accumulate in cancer cells?

A

Enhanced uptake via over-expressed GLUT1

Inability of PFK-1 to further metabolise it in glycolysis

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14
Q

Does the production of ROS in the mitochondria occur in cancer cells under hypoxic conditions?

A

Yes

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15
Q

If p53 doesn’t work, can ROS activate other tumour suppressor proteins?

A

Yes

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16
Q

What are the metabolic challenges of cancer cells?

A

Oxidative stress caused by over-production of ROS in hypoxia
Need precursors and reducing power for synthesis of
- Membrane lipids
- Proteins
- Nucleic acids

17
Q

What are the solutions for the metabolic challenges of cancer cells?

A

Warburg effect reduces use of TCA cycle > less ROS
Synthesis of more anti-oxidants to scavenge ROS
Increased influx for glycolysis and pentose phosphate pathways > production of precursors and NADPH > synthesis

18
Q

What is glutathione?

A

Antioxidant tripeptide

19
Q

What is the relationship between NADPH and antioxidants, including glutathione?

A

Regeneration of oxidised antioxidants, including glutathione

20
Q

How is NADPH generated?

A

In cytosol mainly in pentose phosphate pathway

21
Q

What is the role of the pentose phosphate pathway?

A

Generate NADPH for use in biosynthesis of fatty acids, proteins, amino acids, and nucleic acids
Generate NADPH for regeneration of oxidised antioxidants

22
Q

What are the two phases of the pentose phosphate pathway?

A

Oxidative generation of NADPH

Non-oxidative inter-conversion of sugars

23
Q

How does the non-oxidative inter-conversion of sugars in the pentose phosphate pathway contribute to the synthesis of amino and nucleic acids?

A

Generates variety of carbon backbones

Needed for amino and nucleic acids

24
Q

What is the relationship between glycolysis and the pentose phosphate pathway?

A

Intermediates of glycolysis in excess because of slow PKM2

Can enter pentose phosphate pathway

25
Q

What is the glucose-6-phosphate generated from glycolysis used for in cancer cells?

A

Pentose phosphate pathway

26
Q

What are some metabolic approaches to treat cancer?

A

Dietary restriction to limit glucose availability
Inhibitors of glycogen phosphorylase
Inhibitors of hexokinase
Inhibitors of PKM2