Jantová S, Letasiová S, Repický A, Ovádeková R, Lakatos B
Department of Biochemistry and Microbiology, Faculty of Chemical and Food Technology, Slovak University of Technology, Radlinského 9, SK-81237 Bratislava, Slovak Republic.
Cell Biochem Funct. 2006 Nov-Dec;24(6):519-30. doi: 10.1002/cbf.1296.
Quinazolines are multitarget agents, which have broad spectrum of biological activity, and some of them are now in cancer clinical testing. 3-(5-nitro-2-thienyl)-9-chloro-5-morpholin-4-yl[1,2,4]triazolo[4,3-c]quinazoline is a new synthetically prepared derivative, which in our previous study showed cytotoxic effects on cancer cell lines HeLa and B16. Quinazoline, at micromolar concentrations, induced morphological changes and necrosis of B16 cells, and at nanomolar concentrations it produced changes of F-actin cytoskeleton. It did not cause changes in the cell cycle, did not induce apoptotic cell death in B16 cells, did not have a mutagenic effect, and did not even behave as a typical intercalating agent. Little significant reduction of tumor volume in intramuscular transplanted B16 cells was observed. The aim of the present study was to examine the cytotoxic effect of 3-(5-nitro-2-thienyl)-9-chloro-5-morpholin-4-yl[1,2,4]triazolo[4,3-c]quinazoline on murine leukemia L1210 cells and fibroblast NIH-3T3 cells. Induction of cell morphology and cell cycle changes, induction of apoptosis and caspase 3 activity were studied. Quinazoline acted cytotoxically on both cell lines. The sensitivity of leukemia L1210 cells to the quinazoline was higher than that of fibroblast NIH-3T3. The IC(100) was 12 microM for L1210 cells and 24 microM for NIH-3T3 cells. No effect of quinazoline on the cell cycle profile of L1210 and NIH-3T3 was detected, however, quinazoline induced an increase of the sub-G(0) cell fraction, apoptotic DNA fragmentation, and apoptotic morphological changes at a concentration of 12 microM. This quinazoline concentration induced caspase 3 activity. Our results demonstrated that induction of apoptotic cell death via activation of caspase 3 contributed to the cytotoxic effects of 3-(5-nitro-2-thienyl)-9-chloro-5-morpholin-4-yl[1,2,4]triazolo[4,3-c]quinazoline in murine leukemia L1210 cells.
喹唑啉类是多靶点药物,具有广泛的生物活性,其中一些目前正在进行癌症临床试验。3-(5-硝基-2-噻吩基)-9-氯-5-吗啉-4-基[1,2,4]三唑并[4,3-c]喹唑啉是一种新合成的衍生物,在我们之前的研究中显示对癌细胞系HeLa和B16具有细胞毒性作用。喹唑啉在微摩尔浓度下可诱导B16细胞发生形态变化和坏死,在纳摩尔浓度下可引起F-肌动蛋白细胞骨架的改变。它不会引起细胞周期变化,不会诱导B16细胞凋亡性细胞死亡,没有诱变作用,甚至也不像典型的嵌入剂那样起作用。在肌肉内移植的B16细胞中观察到肿瘤体积仅有轻微的显著减小。本研究的目的是检测3-(5-硝基-2-噻吩基)-9-氯-5-吗啉-4-基[1,2,4]三唑并[4,3-c]喹唑啉对小鼠白血病L1210细胞和成纤维细胞NIH-3T3细胞的细胞毒性作用。研究了细胞形态和细胞周期变化的诱导、凋亡的诱导以及半胱天冬酶3活性。喹唑啉对这两种细胞系均有细胞毒性作用。白血病L1210细胞对喹唑啉的敏感性高于成纤维细胞NIH-3T3。L1210细胞的IC(100)为12微摩尔,NIH-3T3细胞的IC(100)为24微摩尔。未检测到喹唑啉对L1210和NIH-3T3细胞周期分布的影响,然而,喹唑啉在12微摩尔浓度下可诱导亚G(0)期细胞分数增加、凋亡性DNA片段化以及凋亡形态变化。该喹唑啉浓度可诱导半胱天冬酶3活性。我们的结果表明,通过激活半胱天冬酶3诱导凋亡性细胞死亡有助于3-(5-硝基-2-噻吩基)-9-氯-5-吗啉-4-基[1,2,4]三唑并[4,3-c]喹唑啉对小鼠白血病L1210细胞的细胞毒性作用。