Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc
Journal website http://www.jocmr.org

Original Article

Volume 10, Number 11, November 2018, pages 815-821


The Effect of p53 Status on Radio-Sensitivity of Quiescent Tumor Cell Population Irradiated With γ-Rays at Various Dose Rates

Figures

Figure 1.
Figure 1. Surviving fractions following γ-ray irradiation. The clonogenic cell survival curves for total tumor cell populations immediately and 9 h after γ-ray irradiation with high dose-rate irradiation (HDR) and immediately after γ-ray irradiation with middle dose-rate irradiation (MDR) and low dose-rate irradiation (LDR) are shown. The left and right panels show SAS/neo and SAS/mp53 tumor cells, respectively. Bars represent standard errors (n = 6).
Figure 2.
Figure 2. Net micronucleus frequencies following γ-ray irradiation. The net micronucleus frequencies for total (solid lines, open symbols) and quiescent (dotted lines, solid symbols) cell populations immediately and 9 h after γ-ray irradiation with high dose-rate irradiation (HDR) and immediately after γ-ray irradiation with middle dose-rate irradiation (MDR) and low dose-rate irradiation (LDR) are shown. The left and right panels show SAS/neo and SAS/mp53 tumor cells, respectively. Bars represent standard errors (n = 6).

Tables

Table 1. Plating Efficiency and Micronucleus Frequency at 0 Gy
 
Total tumor cellsQuiescent cells
aMean ± standard error (n = 6).
SAS/neo
  Plating efficiency (%)45.5 ± 8.9a
  Micronucleus frequency0.038 ± 0.0060.056 ± 0.007
SAS/mp53
  Plating efficiency (%)23.5 ± 4.1
  Micronucleus frequency0.072 ± 0.0080.111 ± 0.010

 

Table 2. Dose-Modifying Factors Due to a Delayed Assay or Reduced Irradiation Dose Ratea
 
HDRMDRLDR
9h later
aThe ratio of the dose of radiation necessary to obtain each end-point with a delayed assay or reduced dose-rate irradiation to that needed to obtain each end-point with an assay immediately after high dose-rate irradiation. bMean ± standard error (n = 6).
Surviving fraction = 0.2
  SAS/neo1.5 ± 0.15b1.6 ± 0.152.1 ± 0.2
  SAS/mp531.1 ± 0.11.2 ± 0.11.3 ± 0.1
Net micronucleus frequency = 0.1
  Total tumor cells
    SAS/neo1.4 ± 0.11.45 ± 0.11.8 ± 0.15
    SAS/mp531.05 ± 0.11.1 ± 0.11.15 ± 0.1
  Quiescent cells
    SAS/neo1.55 ± 0.151.65 ± 0.151.85 ± 0.2
    SAS/mp531.05 ± 0.11.1 ± 0.11.2 ± 0.1

 

Table 3. Dose-Modifying Factors for SAS/mp53 Relative to SAS/neo Tumor Cellsa
 
HDRHDRMDRLDR
Right after9 h later
aThe ratio of the physical radiation dose of external beams necessary to obtain each end-point in SAS/mp53 tumor cells to that needed to obtain each end-point in SAS/neo tumor cells. bMean ± standard error (n = 6).
Surviving fraction = 0.2
1.4 ± 0.1b1.05 ± 0.11.05 ± 0.11.0 ± 0.1

 

Table 4. Dose-Modifying Factors for Quiescent Relative to Total Tumor Cellsa at Net Micronucleus Frequency of 0.1
 
HDRHDRMDRLDR
Right after9 h later
aThe ratio of the dose of radiation necessary to obtain each end-point in the quiescent cell population to that needed to obtain each end-point in the total tumor cell population. bMean ± standard error (n = 6).
SAS/neo
2.2 ± 0.2b2.2 ± 0.22.4 ± 0.252.45 ± 0.25
SAS/mp53
1.85 ± 0.21.9 ± 0.21.9 ± 0.21.95 ± 0.2