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. 2016 Jun 10;24(17):974–990. doi: 10.1089/ars.2015.6437

Table 1.

GR Number in Growing Melanoma Cells in Mice Treated With Pter and/or CRC

  A2058 MeWo MelJuso
Treatment Tumor vol. (mm3) 103 GR/cell CRC (ng/ml plasma) Tumor vol. (mm3) 103 GR/cell CRC (ng/ml plasma) Tumor vol. (mm3) 103 GR/cell CRC (ng/ml plasma)
None 1049 ± 267 73 ± 6 247 ± 36 507 ± 166 52 ± 4 195 ± 35 286 ± 69 55 ± 5 179 ± 37
Pter 258 ± 66* 71 ± 5 123 ± 29* 167 ± 53* 45 ± 6 87 ± 17* 145 ± 35* 47 ± 4 80 ± 15*
CRC 857 ± 185 80 ± 7 205 ± 48 426 ± 116 49 ± 7 177 ± 29 240 ± 94 46 ± 6 164 ± 41
Pter+CRC 906 ± 214 72 ± 5 196 ± 37 451 ± 159 50 ± 5 186 ± 35 229 ± 77 51 ± 5 175 ± 35

Melanoma cells stably expressing the red fluorescence protein (RFP) were inoculated, as in Figure 1, and allowed to grow for 35 days. Treatment with Pter (as in Fig. 1) and/or costicosterone (using ALZET minipumps [ALZET Osmotic Pumps] and jugular vein catheterism [following manufacturer's instructions]; the mean rate of infusion was 0.3 μg of CRC/h) started 1 week after tumor inoculation. Treatment of tumor-bearing mice with vehicles (DMSO-ethanol for Pter as indicated under the Materials and Methods section; or polyethylene glycol 400 for CRC) did not significantly affect the rate of melanoma growth compared with controls (not shown). The number of GRs (expressed as binding sites/cell) was not significantly different when 72 h cultured A2058-RFP, MeWo-RFP, or MelJuso-RFP cells were compared with their wild-type A2058, MeWo, or MelJuso cell counterparts (not shown). Data for GR number, tumor volume (Tumor vol.), and CRC (blood samples were obtained at 12 h circadian time, Fig. 2) displayed in this table were obtained 35 days after tumor inoculation. All tumors had 50–70 mm3 of volume on day 7 after inoculation. GR number on day 7 was not significantly different from GR number on day 35 (not shown). Data are mean values ± SD of six to seven different animals.

*

Significantly different p < 0.01, comparing all groups versus controls (untreated). Data obtained in melanoma-bearing mice treated with vehicle were not significantly different from those calculated for the untreated group (not shown).

CRC, corticosterone; GR, glucocorticoid receptor; Pter, pterostilbene.

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