Vannini Federica, Chattopadhyay Mitali, Kodela Ravinder, Rao Praveen P N, Kashfi Khosrow
Department of Physiology, Pharmacology and Neuroscience, Sophie Davis School of Biomedical Education, City University of New York Medical School, New York, NY 10031, United States.
School of Pharmacy Health Science Campus, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1.
Redox Biol. 2015 Dec;6:318-325. doi: 10.1016/j.redox.2015.08.014. Epub 2015 Aug 20.
We recently reported the synthesis of NOSH-aspirin, a novel hybrid that releases both nitric oxide (NO) and hydrogen sulfide (H2S). In NOSH-aspirin, the two moieties that release NO and H2S are covalently linked at the 1, 2 positions of acetyl salicylic acid, i.e. ortho-NOSH-aspirin (o-NOSH-aspirin). In the present study, we compared the effects of the positional isomers of NOSH-ASA (o-NOSH-aspirin, m-NOSH-aspirin and p-NOSH-aspirin) to that of aspirin on growth of HT-29 and HCT 15 colon cancer cells, belonging to the same histological subtype, but with different expression of cyclooxygenase (COX) enzymes; HT-29 express both COX-1 and COX-2, whereas HCT 15 is COX-null. We also analyzed the effect of these compounds on proliferation and apoptosis in HT-29 cells. Since the parent compound aspirin, inhibits both COX-1 and COX-2, we also evaluated the effects of these compounds on COX-1 and COX-2 enzyme activities and also performed modeling of the interactions between the positional isomers of NOSH-aspirin and COX-1 and COX-2 enzymes. We observed that the three positional isomers of NOSH aspirin inhibited the growth of both colon cancer cell lines with IC50s in the nano-molar range. In particular in HT-29 cells the IC50s for growth inhibition were: o-NOSH-ASA, 0.04±0.011 µM; m-NOSH-ASA, 0.24±0.11 µM; p-NOSH-ASA, 0.46±0.17 µM; and in HCT 15 cells the IC50s for o-NOSH-ASA, m-NOSH-ASA, and p-NOSH-ASA were 0.062 ±0.006 µM, 0.092±0.004 µM, and 0.37±0.04 µM, respectively. The IC50 for aspirin in both cell lines was >5mM at 24h. The reduction of cell growth appeared to be mediated through inhibition of proliferation, and induction of apoptosis. All 3 positional isomers of NOSH-aspirin preferentially inhibited COX-1 over COX-2. These results suggest that the three positional isomers of NOSH-aspirin have the same biological actions, but that o-NOSH-ASA displayed the strongest anti-neoplastic potential.
我们最近报道了NOSH-阿司匹林的合成,它是一种能释放一氧化氮(NO)和硫化氢(H₂S)的新型杂合物。在NOSH-阿司匹林中,释放NO和H₂S的两个部分在乙酰水杨酸的1、2位共价连接,即邻位-NOSH-阿司匹林(o-NOSH-阿司匹林)。在本研究中,我们比较了NOSH-ASA的位置异构体(o-NOSH-阿司匹林、间位-NOSH-阿司匹林和对位-NOSH-阿司匹林)与阿司匹林对HT-29和HCT 15结肠癌细胞生长的影响,这两种细胞属于同一组织学亚型,但环氧合酶(COX)酶的表达不同;HT-29同时表达COX-1和COX-2,而HCT 15不表达COX。我们还分析了这些化合物对HT-29细胞增殖和凋亡的影响。由于母体化合物阿司匹林能抑制COX-1和COX-2,我们还评估了这些化合物对COX-1和COX-2酶活性的影响,并对NOSH-阿司匹林的位置异构体与COX-1和COX-2酶之间的相互作用进行了建模。我们观察到,NOSH阿司匹林的三种位置异构体均能抑制这两种结肠癌细胞系的生长,其半数抑制浓度(IC50)在纳摩尔范围内。特别是在HT-29细胞中,生长抑制的IC50分别为:o-NOSH-ASA,0.04±0.011µM;间位-NOSH-ASA,0.24±0.11µM;对位-NOSH-ASA,0.46±0.17µM;在HCT 15细胞中,o-NOSH-ASA、间位-NOSH-ASA和对位-NOSH-ASA的IC50分别为0.062±0.006µM、0.092±0.004µM和0.37±0.04µM。在24小时时,两种细胞系中阿司匹林的IC50均>5mM。细胞生长的减少似乎是通过抑制增殖和诱导凋亡来介导的。NOSH-阿司匹林的所有3种位置异构体对COX-1的抑制作用均优先于COX-2。这些结果表明,NOSH-阿司匹林的三种位置异构体具有相同的生物学作用,但o-NOSH-ASA显示出最强的抗肿瘤潜力。