Pleiotropic effects of the sirtuin inhibitor sirtinol involves concentration-dependent modulation of multiple nuclear receptor-mediated pathways in androgen-responsive prostate cancer cell LNCaP

• Published in: Molecular carcinogenesis Vol. 52; no. 9; pp. 676 - 685
• Main Authors: Wang, Thomas T.Y., Schoene, Norberta W., Kim, Eun-Kyung, Kim, Young S.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2013; Wiley Subscription Services, Inc
• Subjects: androgen; Androgens; Androgens - genetics; Androgens - metabolism; Anticarcinogenic Agents - pharmacology; Benzamides - pharmacology; Cell Cycle - drug effects; Cell Cycle - genetics; Cell Line, Tumor; Cell Proliferation - drug effects; Cyclin-Dependent Kinase Inhibitor p21 - genetics; Cyclin-Dependent Kinase Inhibitor p21 - metabolism; Cytochrome P-450 CYP1A1 - genetics; Cytochrome P-450 CYP1A1 - metabolism; estrogen; Estrogens - genetics; Estrogens - metabolism; Humans; Insulin-Like Growth Factor I - genetics; Insulin-Like Growth Factor I - metabolism; insulin-like growth factor-1; Male; NAD(P)H Dehydrogenase (Quinone) - genetics; NAD(P)H Dehydrogenase (Quinone) - metabolism; Naphthols - pharmacology; Phytotherapy; Prostatic Neoplasms - drug therapy; Prostatic Neoplasms - genetics; Prostatic Neoplasms - metabolism; Receptors, Cytoplasmic and Nuclear - genetics; Receptors, Cytoplasmic and Nuclear - metabolism; Signal Transduction - drug effects; Signal Transduction - genetics; sirtinol; sirtuin; Sirtuins - antagonists & inhibitors; Sirtuins - genetics; Sirtuins - metabolism; Up-Regulation - drug effects; xenobiotic metabolism; insulin-like growth factor-1; androgen; estrogen; sirtinol; sirtuin; xenobiotic metabolism
• ISSN: 0899-1987; 1098-2744
• DOI: 10.1002/mc.21906

Sirtinol is a purported specific inhibitor of the nicotinamide adenine dinucleotide (NAD)‐dependent type III histone deacetylase (also known as sirtuin). Sirtinol has been used extensively to identify chemopreventive/chemotherapeutic agents that modulate the sirtuins. However, the molecular effect of sirtinol other than serving as sirtuin inhibitor in cells is less clear. The present study addressed this deficiency in the literature. Based on structural similarity with plant‐derived cancer preventive/therapeutic compounds such as 3', 3'‐diindolylmethane, resveratrol, and genistein, we hypothesized that sirtinol may act on pathways similar to that affected by these compounds in the human prostate cancer cell LNCaP. We found that treatment of LNCaP cells with sirtinol led to concentration‐dependent effects on multiple pathways. Sirtinol inhibited LNCaP cell cycle and growth that was correlated with up‐regulation of cyclin‐dependent kinase inhibitor 1A mRNA and protein levels. This effect of sirtinol may due in part to modulation of androgen, estrogen, and insulin‐like growth factor‐1 mediated pathways as sirtinol treatment led to inhibition of mRNA and protein expression of marker genes involved in these pathways. We also found sirtinol activates aryl hydrocarbon‐dependent pathways in LNCaP cells. The effects of sirtinol were observed at 25 µM, a concentration lower than Ki (38 µM) for sirtuin activity. Based on these results we reasoned that sirtinol exerts pleiotropic effects in cells and that biological effects of sirtinol may not be due solely to inhibition of sirtuin. © 2012 Wiley Periodicals, Inc.