Effect of 2, 5-dimethylphenol on Ca2+ movement and viability in PC3 human prostate cancer cells. (12th June 2016)

• Record Type: Journal Article
• Authors: Wang, Jue-Long; Chou, Chiang-Ting; Liang, Wei-Zhe; Yeh, Jeng-Hsien; Kuo, Chun-Chi; Lee, Chao-Ying; Shieh, Pochuen; Kuo, Daih-Huang; Chen, Fu-An; Jan, Chung-Ren
• Is Part Of: Toxicology mechanisms and methods. Volume 26:Number 5(2016)
• Page Start: 327
• Page End: 333
• Publication Date: 2016-06-12
• Subjects: Ca2+ -- 2, 5-dimethylphenol -- endoplasmic reticulum -- phospholipase C -- prostate cancer cells -- store-operated Ca2+ entry; Analytical toxicology -- Periodicals; Toxicology -- Periodicals; Toxicology -- Methodology -- Periodicals; 615.907
• DOI: 10.3109/15376516.2016.1158893
• Languages: English
• ISSNs: 1537-6516

Abstract

Abstract: The phenolic compound 2, 5-dimethylphenol is a natural product. 2, 5-Dimethylphenol has been shown to affect rat hepatic and pulmonary microsomal metabolism. However, the effect of 2, 5-dimethylphenol on Ca 2+ signaling and cyotoxicity has never been explored in any culture cells. This study explored the effect of 2, 5-dimethylphenol on cytosolic free Ca 2+ levels ([Ca 2+ ]i ) and cell viability in PC3 human prostate cancer cells. 2, 5-Dimethylphenol at concentrations between 500 μM and 1000 μM evoked [Ca 2+ ]i rises in a concentration-dependent manner. This Ca 2+ signal was inhibited by approximately half by the removal of extracellular Ca 2+ . 2, 5-Dimethylphenol-induced Ca 2+ influx was confirmed by Mn 2+ -induced quench of fura-2 fluorescence. Pretreatment with the protein kinase C (PKC) inhibitor GF109203X, nifedipine or the store-operated Ca 2+ entry inhibitors (econazole or SKF96365) inhibited 2, 5-dimethylphenol-induced Ca 2+ signal in Ca 2+ -containing medium by ∼30%. Treatment with the endoplasmic reticulum Ca 2+ pump inhibitor thapsigargin in Ca 2+ -free medium abolished 2, 5-dimethylphenol-induced [Ca 2+ ]i rises. Conversely, treatment with 2, 5-dimethylphenol abolished thapsigargin-induced [Ca 2+ ]i rises. Inhibition of phospholipase C (PLC) with U73122 reduced 2, 5-dimethylphenol-evoked [Ca 2+ ]i rises by ∼80%. 2, 5-Dimethylphenol killed cells at concentrations of 350–1000 μM in a concentration-dependent fashion. Chelation of cytosolic Ca 2+ with 1, 2-bis(2-aminophenoxy)ethane- N, N, N ′, N ′-tetraacetic acid/AM (BAPTA/AM) did not prevent 2, 5-dimethylphenol's cytotoxicity. Together, in PC3 cells, 2, 5-dimethylphenol induced [Ca 2+ ]i rises that involved Ca 2+ entry through PKC-regulated store-operated Ca 2+ channels and PLC-dependent Ca 2+ release from the endoplasmic reticulum. 2, 5-Dimethylphenol induced cytotoxicity in a Ca 2+ -independent manner.