TABLE R.60
Mechanisms of Resveratrol in Cells In Vitro Related to Cancer Chemoprevention
Mechanism | Experimental system | “Efficacious” concentrations (μM)a |
---|---|---|
Inhibition of growth | Multiple cell lines | ~5–10 |
Induction of apoptosis | Leukemia cells | 32–100 |
Induction of p53-independent apoptosis | Colon tumor cells | 100 |
Estrogen agonism | Mammary cells | 10–25 |
Antiestrogenicity | Mammary cells | 0.1–1 |
Inhibition of oxygen radical formation nitric oxide production | Macrophages | ~30 |
Inhibition of cytochrome P450 enzymes: CYP1A1 CYP1B1, CYP3A4 | Liver cells, microsomes, recombinant enzyme | 1–20 |
Activation of p53 | Mouse epidermal cells | 20 |
Activation of c-jun kinase | Mouse epidermal cells | 10–40 |
Decrease in COX-2 expression | Mammary epithelial cells | ~5 |
Increase in p21/Cipl, cyclins D1, D2, E; decrease in cdks 2,4,6 | Epidermoid carcinoma cells | ~10 |
Increase in cyclins A, B1, and cdks 1 and 2 | Colon tumor cells | 30 |
Inhibition of protein kinase C activity | Gastric cells | 50 |
Inhibition of protein kinase D activity | Fibroblasts | >100 |
Inhibition of NF-κBb activation | Monocytes, macrophages | 30 |
Inhibition of NF-κB and AP-1 activation | Myeloid, lymphoid, epithelial cells | 5 |
a Lowest concentrations at which reproducible changes have been observed, or IC50 or EC50, if provided.
b NF-κB, nuclear factor κB.
Source: From Gescher and Steward, Cancer Epidemiol. Biomarkers Prev., 12:953–957, 2003. With permission.