Moalic S, Liagre B, Le Bail J C, Beneytout J L
UPRES EA 1085, Laboratory of Biochemistry, Faculty of Pharmacy, Limoges, France.
Int J Oncol. 2001 Mar;18(3):533-40. doi: 10.3892/ijo.18.3.533.
A selective cyclooxygenase-2 (COX-2) inhibitor, NS-398, was shown to produce an anti-proliferative and pro-apoptotic effect on different types of cell lines. We describe the presence of COX-1 and COX-2 pathways in the human osteosarcoma 1547 cell line, as well as the conflicting effects of NS-398 (10, 50 and 100 microM) on programmed cell death, PGE2 release and COX-2 expression in 1547 cells cultured under apoptotic conditions. We demonstrate a link between the effects of 10 and 100 microM NS-398 on cell apoptosis, PGE2 release, and expression of COX-2 in 1547 cells undergoing apoptosis. At 10 microM, NS-398 acted as a selective COX-2 inhibitor moderately increasing apoptosis without any effect on COX-2 expression. In contrast, at 100 microM, NS-398 induced a cell cycle slowing or arrest, strongly enhanced COX-2 expression which was associated with a high PGE2 release and a marked decrease in apoptosis. This latter property of NS-398 at 100 microM in 1547 human osteosarcoma cells is novel compared to the described NS-398 pro-apoptotic effect on other cell lines.
选择性环氧化酶-2(COX-2)抑制剂NS-398已被证明对不同类型的细胞系具有抗增殖和促凋亡作用。我们描述了人骨肉瘤1547细胞系中COX-1和COX-2途径的存在,以及NS-398(10、50和100微摩尔)在凋亡条件下培养的1547细胞中对程序性细胞死亡、前列腺素E2(PGE2)释放和COX-2表达的矛盾影响。我们证明了10和100微摩尔NS-398对1547细胞凋亡、PGE2释放和COX-2表达的影响之间存在联系。在10微摩尔时,NS-398作为一种选择性COX-2抑制剂,适度增加凋亡,对COX-2表达无任何影响。相比之下,在100微摩尔时,NS-398诱导细胞周期减慢或停滞,强烈增强COX-2表达,这与高PGE2释放和凋亡显著减少相关。与NS-398对其他细胞系的促凋亡作用相比,NS-398在100微摩尔时对1547人骨肉瘤细胞的后一种特性是新颖的。