Kim Kyung-Su, Yoon Joo-Heon, Kim Jin Kook, Baek Seung Joon, Eling Thomas E, Lee Won Jae, Ryu Ji-Hwan, Lee Jeung Gweon, Lee Joo-Hwan, Yoo Jong-Bum
Department of Otorhinolaryngology, Yonsei University College of Medicine, 134 Shinchon-dong, Seodaemoon-gu, Seoul, Republic of Korea.
Biochem Biophys Res Commun. 2004 Dec 24;325(4):1298-303. doi: 10.1016/j.bbrc.2004.10.176.
We have investigated whether NAG-1 is induced in oral cavity cancer cells by various NSAIDs and if apoptosis induced by NSAIDs can be linked directly with the induction of NAG-1. NAG-1 expression was increased by diclofenac, aceclofenac, indomethacin, ibuprofen, and sulindac sulfide, in the order of NAG-1 induction, but not by acetaminophen, piroxicam or NS-398. Diclofenac was the most effective NAG-1 inducer. Incubation with diclofenac inhibited cell proliferation and induced apoptosis. The expression of NAG-1 was observed in advance of the induction of apoptosis. Conditioned medium from NAG-1-overexpressing Drosophila cells inhibited SCC 1483 cells proliferation and induced apoptosis. In summary, some NSAIDs induce NAG-1 expression in oral cavity cancer cells and the induced NAG-1 protein appears to mediate apoptosis. Therefore, NSAIDs may be considered as a possible chemopreventive agent against oral cavity cancer.
我们研究了多种非甾体抗炎药(NSAIDs)是否能在口腔癌细胞中诱导生长抑制和DNA损伤诱导基因1(NAG-1)表达,以及NSAIDs诱导的细胞凋亡是否能直接与NAG-1的诱导相关联。双氯芬酸、醋氯芬酸、吲哚美辛、布洛芬和舒林酸硫化物可增加NAG-1表达,按NAG-1诱导顺序排列,但对乙酰氨基酚、吡罗昔康或NS-398则无此作用。双氯芬酸是最有效的NAG-1诱导剂。用双氯芬酸孵育可抑制细胞增殖并诱导细胞凋亡。NAG-1的表达在细胞凋亡诱导之前就已观察到。来自过表达NAG-1的果蝇细胞的条件培养基可抑制SCC 1483细胞增殖并诱导细胞凋亡。总之,一些NSAIDs可在口腔癌细胞中诱导NAG-1表达,且诱导的NAG-1蛋白似乎介导细胞凋亡。因此,NSAIDs可被视为预防口腔癌的一种可能的化学预防剂。