Annatto constituent cis-bixin has selective antimyeloma effects mediated by oxidative stress and associated with inhibition of thioredoxin and thioredoxin reductase

• Published in: Antioxidants & redox signaling Vol. 13; no. 7; p. 987
• Main Authors: Tibodeau, Jennifer D, Isham, Crescent R, Bible, Keith C
• Format: Journal Article
• Language: English
• Published: United States 01.10.2010
• Subjects: Acetylcysteine - metabolism; Acetylcysteine - pharmacology; Antineoplastic Agents - pharmacology; Antineoplastic Agents - therapeutic use; Apoptosis - drug effects; Bixaceae; Carotenoids - pharmacology; Cell Line, Tumor; Cell Survival - drug effects; Drug Screening Assays, Antitumor; Glutathione - metabolism; Glutathione - pharmacology; Humans; Multiple Myeloma - drug therapy; Multiple Myeloma - pathology; Oxidation-Reduction; Oxidative Stress - drug effects; Phytotherapy; Plant Extracts; Reactive Oxygen Species - metabolism; Seeds; Thioredoxin-Disulfide Reductase - antagonists & inhibitors; Thioredoxin-Disulfide Reductase - metabolism; Thioredoxins - antagonists & inhibitors; Thioredoxins - metabolism
• ISSN: 1557-7716
• DOI: 10.1089/ars.2009.2896

In pursuit of the anticancer effects of seeds of the rain forest plant Bixa orellana (annatto), we found that its constituent cis-bixin induced cytotoxicity in a wide variety of tumor cell lines (IC(50) values from 10 to 50 microM, 24-h exposures) and, importantly, also selectively killed freshly collected patient multiple myeloma cells and highly drug-resistant multiple myeloma cell lines. Mechanistic studies indicated that cis-bixin-induced cytotoxicity was greatly attenuated by co-treatment with glutathione or N-acetylcysteine (NAC); whereas fluorescence-activated cell sorting (FACS) assays using the cell-permeable dyes 5-(and-6) chloromethyl-2',7'-dichlorodihydrofluorescein diacetate, acetyl ester (CM-H(2)DCFDA), or dihydroethidium demonstrated that cis-bixin rapidly induced cellular reactive oxygen species (ROS) in dose- and time-dependent fashions, collectively implicating ROS as contributory to cis-bixin-induced cytotoxicity. In pursuit of potential contributors to ROS imposition by cis-bixin, we found that cis-bixin inhibited both thioredoxin (Trx) and thioredoxin reductase (TrxR1) activities at concentrations comparable to those required for cytotoxicity, implicating the inhibition of these redox enzymes as potentially contributing to its ability to impose cellular ROS and to kill cancer cells. Collectively, our studies indicate that the annatto constituent cis-bixin has intriguing selective antimyeloma activity that appears to be mediated through effects on redox signaling.