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. 2013 Jan;168(1):79–102. doi: 10.1111/j.1476-5381.2012.02027.x

Table 2.

Effect of plant cannabinoids on the viability of human prostate carcinoma androgen receptor-positive (LNCaP) cells

Pure compound IC50 (µM) on cell viability [A] IC50 (µM) on cell viability [B] BDS IC50 (µM) on cell viability [A] IC50 (µM) on cell viability [B]
CBD 25.0 ± 3 5.7 ± 2 CBD BDS 18.1 ± 6 6.6 ± 2
CBC 20.0 ± 5 10.9 ± 3 CBC BDS >25 (25.6%) 7.9 ± 1
CBG >25 (34.5%) 11.2 ± 4 CBG BDS 21 ± 8 9.0 ± 1
CBDV >25 (27.6%) 20.0 ± 3 CBDV BDS >25 (24.4%) 10.4 ± 1
THCV >25 (28.5%) 17.5 ± 3 THCV BDS 16.3 ± 5 7.2 ± 1
THCVA >25 (32.4%) 11.5 ± 5 THCVA BDS 19.4 ± 8 5.6 ± 1
THCA 22.1 ± 2 17.1 ± 1 THCA BDS 15.0 ± 2 4.0 ± 3
CBDA >25 (30.2%) 16.2 ± 5 CBDA BDS >25 (34.5%) 9.3 ± 2
CBGA >25 (7.0%) 11.6 ± 2 CBGA BDS 14.5 ± 2 8.5 ± 2
CBGV >25 (23.9%) >25 (41.0%) CBGV BDS >25 (40.2%) 9.4 ± 2
CBN 14.5 ± 6 >25 (34.2%)
THC 16.9 ± 3 5.5 ± 3

(A) Cells were seeded in presence of 10% FBS in six-well Multiwell with a density of 1 × 105 cells·per well. After adhesion, cells were treated with increasing concentrations of compounds for 72 h (presence of serum was maintained during the treatments). (B) Cells were seeded in presence of 10% FBS in six-well Multiwell with a density of 1 × 105 cells·per well. After adhesion, cells were starved for 16 h and subsequently treated with increasing concentrations of compounds for 24 h (absence of serum was maintained during the treatments). Cell viability was assessed by MTT staining. Data are reported as mean ± SD of IC50 values calculated from three independent experiments. In the case of IC50 > 25 µM, the maximum inhibition observed at the highest concentration tested (25 µM) is shown.