Seminar 9 - Radiotherapy in cancer management Flashcards

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1
Q

Outline the types of radiation therapy.

A
  1. External beam radiotherapy
  2. Brachytherapy - sealed sources
  3. Unsealed sources: radioiodine - thyroid cancer, meta-iodobenzylG - neuroblastoma
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2
Q

Describe the Compton process.

A
  • High energy photons
  • Photons interacts with loosely bound free electrons of low energy
  • Part of photon energy is given to electron as KE
  • Photon is deflected and proceeds with a reduced energy: longer wavelength
  • The end result is the production of fast electrons, which may go on to ionise other atoms of the absorber, plus a deflected/scattered photon with lower energy
  • Independent of the atomic number of the absorbing species
  • In radiation therapy, important to avoid the problem of differential absorption in tissues - bone vs. soft tissue
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3
Q

Describe the photoelectric process.

A

Photons of lower energy - diagnostic radiology

  • Photons interact with tightly bound electrons of higher binding energy
  • Photon gives up its energy entirely
  • Electron is ejected, and the photon is entirely absorbed
  • End result is production of fast electrons but the photon is entirely absorbed
  • Varies rapidly with the atomic number (Z^4)
  • Diagnostic radiology - photoelectric process is important because bone differentially absorbs X-rays, resulting in the familiar appearance of radiographs
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4
Q

Describe the spindle assembly checkpoint.

A
  • Quality control checkpoint
  • Allows mitosis to progress only if the chromosomes are properly attached to the spindle apparatus
  • If there is the “GO” signal, SAC promotes degradation of cyclin B and allows mitosis to progress
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5
Q

What is APC/C?

A

The anaphase promoting complex - E3 ubiquitin ligase which promotes degradation of cyclin B1 and securin

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6
Q

State the components of SAC.

A
  1. BubR1
  2. MAD2
  3. BUB3
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7
Q

Distinguish between the direct and indirect effects of ionising radiation.

A
  1. Direct: ionising radiation interacts with the atoms of the target molecule (DNA) –> ionised: generally cannot be modified by sensitisers and protectors
  2. Indirect: ionising radiation interacts with other molecules to produce free radicals that migrate to the DNA
    - Accounts for 2/3rds of cellular damage, modified by sensitisers and protectors
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8
Q

Outline the features of spurs and blobs.

A

Spur: 4nm diameter, 3 ion pairs
Blob: 7 nm diameter, 12 ion pairs

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9
Q

What is the biological effect of ionising radiation determined by?

A

Not by amount of energy absorbed, but photon energy size

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10
Q

What type of damage does interaction of ionising radiation with DNA cause?

A
  1. Base damage: thymine glycols, 8-hydroxyguanine
  2. Sugar damage: abasic sites, strand break lesions
  3. Strand breaks: single strand breaks, double strand breaks
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