Otto-Ślusarczyk Dagmara, Graboń Wojciech, Mielczarek-Puta Magdalena, Chrzanowska Alicja
Chair and Department of Biochemistry, Medical University of Warsaw, 02-097 Warsaw, Banacha 1, Poland.
Biochem Biophys Rep. 2021 Sep 23;28:101141. doi: 10.1016/j.bbrep.2021.101141. eCollection 2021 Dec.
Leflunomide (LFN) is a well-known immunomodulatory and anti-inflammatory prodrug of teriflunomide (TFN). Due to pyrimidine synthesis inhibition TFN also exhibits potent anticancer effect. Because, there is the strict coupling between the pyrimidine synthesis and the mitochondrial respiratory chain, the oxygen level could modify the cytostatic TNF effect. The aim of the study was to evaluate the cytostatic effect of pharmacologically achievable teriflunomide (TFN) concentrations at physiological oxygen levels, i.e. 1% hypoxia and 10% tissue normoxia compared to 21% oxygen level occurred in routine cell culture environment. The TFN effect was evaluated using TB, MTT and FITC Annexin tests for human primary (SW480) and metastatic (SW620) colon cancer cell lines at various oxygen levels. We demonstrated significant differences between proliferation, survival and apoptosis at 1, 10 and 21% oxygen in primary and metastatic colon cancer cell lines (SW480, SW620) under TFN treatment. The cytostatic TFN effect was more pronounced at hypoxia compared to tissue and atmospheric normoxia in both cancer cell lines, however metastatic cells were more resistant to antiproliferative and proapoptotic TFN action. The early apoptosis was predominant in physiological oxygen tension while in atmospheric normoxia the late apoptosis was induced. Our findings showed that anticancer TFN effect is more strong in physiological oxygen compared to atmospheric normoxia. It suggests that results obtained from studies could be underestimated. Thus, it gives assumption for future comprehensive studies at real oxygen environment involving TNF use in combination with other antitumor agents affecting oxygen-dependent pyrimidine synthesis.
来氟米特(LFN)是一种广为人知的免疫调节和抗炎前药,可转化为特立氟胺(TFN)。由于TFN抑制嘧啶合成,它还具有强大的抗癌作用。因为嘧啶合成与线粒体呼吸链之间存在严格的耦合关系,所以氧水平可能会改变TFN的细胞生长抑制作用。本研究的目的是评估在生理氧水平下,即可达到的药理学浓度的特立氟胺(TFN)在1%低氧和10%组织常氧环境下的细胞生长抑制作用,与常规细胞培养环境中21%的氧水平进行比较。在不同氧水平下,使用噻唑蓝(TB)、MTT和异硫氰酸荧光素标记的膜联蛋白(FITC Annexin)检测法评估TFN对人原发性(SW480)和转移性(SW620)结肠癌细胞系的作用。我们证明,在TFN处理下,原发性和转移性结肠癌细胞系(SW480、SW620)在1%、10%和21%氧水平下,细胞增殖、存活和凋亡存在显著差异。在两种癌细胞系中,与组织常氧和大气常氧相比,低氧条件下TFN的细胞生长抑制作用更明显,然而转移性细胞对TFN的抗增殖和促凋亡作用更具抗性。在生理氧张力下,早期凋亡占主导,而在大气常氧下则诱导晚期凋亡。我们的研究结果表明,与大气常氧相比,TFN在生理氧环境中的抗癌作用更强。这表明从以往研究中获得的结果可能被低估。因此,这为未来在真实氧环境下进行全面研究提供了假设,这些研究涉及TFN与其他影响氧依赖性嘧啶合成的抗肿瘤药物联合使用。