Guest Lecture: Protein and Cancer Flashcards

1
Q

muscle protein balance

A
  • synthesis = breakdown
  • anabolism: synthesis > breakdown
  • catabolism: synthesis < breakdown
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2
Q

regulators of protein synthesis

A
  • resistance exercise (prolonged upregulation past 48 hrs)
  • ingestion of high-quality protein (leucine/arginine signaling via mTOR)
  • hormone signals (insulin, IGF-1, testosterone) to stimulate mTOR pathway
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3
Q

regulators of protein breakdown

A
  • resistance exercise (rate returns to baseline after 48 hrs
  • early starvation/ low EAA
  • stress/injury/illness (inflammation): signaling cascades connected to autophagy genes and ubiquitin-proteosome pathway; cortisol, epinephrine, glucagon
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4
Q

What is the RLS in protein synthesis?

A

Leucine so really need to make sure we get it

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5
Q

How do we measure muscle?

A
  • DEXA
  • CT scans
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6
Q

Application of CT scans

A

can reveal abnormalities in muscles
* muscle mass correlates with cross-sectional area at L3 (cm2)
* intermuscular adipose tissue: marbling in the muscle
* mean muscle attenuation: lipid content inside muscle cells

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7
Q

How is muscle protein balance affected by cancer?

A

on average lose but is opportunity for protein synthesis

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8
Q

How does cancer associated muscle change correlate with age related muscle change?

A
  • age associated muscle loss is estimated to be a gradual loss of muscle mass of 0.3% to 0.8% per year after middle age, up to 1% per year by age 75. Can potentially be overcome with greater volumes of resistance exercise or greater doses of protein.
  • for cancer patients (especially pancreatic cancer) can be up to 30% in just 4 months
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9
Q

Why is protein loss particularly bad in pancreatic cancer?

A

pancreas plays a major role in synthesis

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10
Q

Why is protein loss particularly bad in pancreatic cancer?

A

pancreas plays a major role in synthesis

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11
Q

Why does muscle change matter to a person recieving cancer treatment?

A

May cause loss of tolerance for treatment because with chemo it has impact for about 2 weeks trying to knock out the rapid cell growth so need people to be able to recover quickly if losing a bunch of neutrophils and with less msucle mass they cannot keep up.
* treatment intolerance → increased infection → decreased function → decreased quality of life →living just to survive

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12
Q

Survival of patients with muscle loss vs no loss, advanced pancreatic cancer

A
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13
Q

Causes of muscle loss in cqncer

A
  • Increased protein requirements for body cell repair/healing after radiation and cytotoxic chemo
  • Elevated energy expenditure in some cases mostly at resting state
  • tumour is a leech and wants all of the nutrients and you CANNOT starve it
  • Altered absorption in some GI cancers
  • reduced food intake
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14
Q

Causes of reduced food intake

A
  • fatigue-loss of desire to eat
  • side effects-altered/loss of taste
  • knowledge-confusion around food for prevention vs. treatment
  • financial-difficult to afford quality product
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15
Q

If we meet energy and protein requirements, can we prevent muscle loss in cancer?

A

No but it can be slowed down, causes for muscle loss in cancer is mainly due to cachexia

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16
Q

describe cancer cachexia

A

loss of skeletal muscle ± adipose tissue which cannot be reversed by nutrient provision, driven by a variable combination of:
* reduced food intake via treatment induced and/or tumour induced (CNS driven) loss of appetite
* altered metabolism elevating EE, increasing systemic inflammation and excess catabolism

17
Q

What reduced food intake is unique to cachexia?

A

tumour-induced, CNS-driven loss of appetite
* always feels like they just ate a massive thanksgiving dinner

18
Q

What happens with systemic inflammation with cachexia?

A

tumor or immune-mediated cytokine release to the liver (interleukin-6, interleukin-1, TNF) altering levels of acute phase proteins (increased c-reactive protein, decreased albumin) and leads to anorexia, insulin resistance, and muscle breakdown

19
Q

What occurs with tumour-induced catabolism in cachexia?

A
  • tumours secrete molecules that directly elicit catabolism
20
Q

How does treatment contribute to cachexia

A

pro-inflammatory factors elicit catabolism
* targeted therapy: drugs that directly target mTOR pathway
* glucocorticoids used mainly for palliation of side effects, but high doses are given in
hematological malignancy
certain chemotherapies are platinum-based cytotoxic drugs

21
Q

potential therapeutics

A
  • theropeutic diet counselling
  • branched chain amino acids
  • possible role of creatine, carnitine, glutamine and arginine
  • multi-modal therapeutics
  • enobosarm oral drug
  • anamorelin oral drug
22
Q

Therapeutic targets under investigation

A
  • reduce inflammation
  • provide adequate nutrients
  • stimulate synthesis
  • inhibit breakdown
23
Q

muscle loss in cancer results from?

A

reduced muscle protein synthesis AND increased breakdown
* Driven by a variable combination of reduced intake and altered metabolism
* Cannot be reversed solely by provision of adequate nutrients
* has significant impact on patient experience and treatment outcomes

24
Q

What is essential to the study and treament of cachexia?

A

a mutli-disciplinary team
* nutrition
* symptom management
* pharmaceuticals
* physiotherapy