Krzyzankova Miroslava, Chovanova Silvia, Chlapek Petr, Radsetoulal Matej, Neradil Jakub, Zitterbart Karel, Sterba Jaroslav, Veselska Renata
Laboratory of Tumor Biology, Department of Experimental Biology, School of Science, Masaryk University, Kotlarska 2, 611 37, Brno, Czech Republic.
Tumour Biol. 2014 Aug;35(8):7617-27. doi: 10.1007/s13277-014-2019-5. Epub 2014 May 6.
The induced differentiation of tumor cells into mature phenotypes is a promising strategy in cancer therapy. In this study, the effects of combined treatment with all-trans retinoic acid (ATRA) and lipoxygenase/cyclooxygenase inhibitors were examined in two osteosarcoma cell lines, Saos-2 and OSA-01. Caffeic acid and celecoxib were used as inhibitors of 5-lipoxygenase and of cyclooxygenase-2, respectively. Changes in the cell proliferation, matrix mineralization, and occurrence of differentiation markers were evaluated in treated cell populations at intervals. The results confirmed the capability of caffeic acid to enhance the antiproliferative effect of ATRA in both cell lines. In contrast, celecoxib showed the same effect in Saos-2 cells only. Furthermore, the extension of matrix mineralization was observed after combined treatment with ATRA and celecoxib or caffeic acid. The increased expression of osteogenic differentiation markers was observed in both cell lines after the combined application of ATRA and inhibitors. The obtained results clearly demonstrate the capability of lipoxygenase/cyclooxygenase inhibitors to enhance the antiproliferative and differentiating effect of ATRA in osteosarcoma cells, although some of these effects are specific and depend on the biological features of the respective tumor or cell line.
将肿瘤细胞诱导分化为成熟表型是癌症治疗中一种很有前景的策略。在本研究中,检测了全反式维甲酸(ATRA)与脂氧合酶/环氧化酶抑制剂联合治疗对两种骨肉瘤细胞系Saos-2和OSA-01的影响。分别使用咖啡酸和塞来昔布作为5-脂氧合酶和环氧化酶-2的抑制剂。定期评估处理后的细胞群体中细胞增殖、基质矿化及分化标志物的出现情况。结果证实咖啡酸能够增强ATRA对两种细胞系的抗增殖作用。相比之下,塞来昔布仅在Saos-2细胞中显示出相同效果。此外,在ATRA与塞来昔布或咖啡酸联合治疗后观察到基质矿化有所扩展。在ATRA与抑制剂联合应用后,两种细胞系中均观察到成骨分化标志物的表达增加。所得结果清楚地表明脂氧合酶/环氧化酶抑制剂能够增强ATRA对骨肉瘤细胞的抗增殖和分化作用,尽管其中一些作用具有特异性且取决于各自肿瘤或细胞系的生物学特性。