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2. Two types of interactions can occur: either a direct hit or an indirect hit.
3. There are four phases in the cell cycle: M, G1, S, and G2.
4. If x-rays acted uniformly, there would be no wasted x-rays, and the number of
surviving cells after a dose equal to D0 is zero.
6. We measure survival of cells instead of cell death because the lethal effects of radiation
are determined by observing cell survival, not cell death.
7. The three numerical parameters attendant to multitarget, single-hit kinetics are D0; the
extrapolation number “n,” also known as the target number; and the radiation dose D.
8. The single cell survival parameter “n,” the extrapolation number, is representative of
the number of targets.
9. The RBE and OER are both measures of radiosensitivity of biologic tissue. For low-
LET radiation the OER is highest, the RBE is lowest. For high LET, the reverse is true.
10. They migrate within the cell, transferring energy to target molecules, and ultimately
join with another molecule to be neutralized.
11. That each cell contains a target site(s) on a target molecule, which must be hit in order
to cause cell death.
12. Radiation exposure of tissue is rather uniform because tissue is large on the x-ray
scale. However, radiation interaction with target molecules is random.
14. In vitro refers to irradiation that occurs outside the body or outside the cell; in vivo
irradiation is irradiation of macromolecules in the living cell.
15. D0 is the parameter that measures the ability of the cell to recover from sublethal
radiation damage.
18. A direct effect exists when the ionizing radiation interacts directly with the target
molecule DNA. An indirect effect occurs when the interaction is resulting from free
radicals transferring their energy to DNA.
19. The cell is most sensitive during the M phase and least sensitive during the last S
phase.