Gorska-Ponikowska Magdalena, Kuban-Jankowska Alicja, Daca Agnieszka, Nussberger Stephan
Department of Medical Chemistry, Medical University of Gdansk, Gdansk, Poland
Department of Biophysics, Institute of Biomaterials and Biomolecular Systems, University of Stuttgart, Stuttgart, Germany.
Cancer Genomics Proteomics. 2017 Nov-Dec;14(6):483-493. doi: 10.21873/cgp.20058.
BACKGROUND/AIM: According to the reverse Warburg effect, tumor cells may metabolize lactate as an energy source and shuttle L-lactate to neighboring cancer cells, adjacent stroma, and vascular endothelial cells, thus inducing metabolic reprogramming. An increased tumor L-lactate level strictly correlates with increased metastasis, tumor recurrence and a poor outcome. A potent anticancer agent that may act on L-lactate activated cells is 2-metoxyestradiol. Thus, the aim of the study was to evaluate whether a potent anticancer agent, 2-methoxyestradiol, is able to reverse L-lactate-induced metabolic reprogramming in osteosarcoma 143B cells.
We used flow cytometry in order to determine cell death, autophagy, expression of KI-67, mitochondrial membrane depolarization. We performed cell proliferation assay in order to determine cell viability and cell migration assay to determine invasive potential of osteosarcoma cells. While, CalcuSyn software was used in order to evaluate the interaction between 2-methoxyestradiol and L-lactate.
We demonstrated that 2-methoxyestradiol abolished L-lactate-induced migration and proliferation of osteosarcoma cells. Moreover, we observed that this effect was associated with regulation of Ki-67 and induction of autophagy.
2-Methoxyestradiol is a potent anticancer agent also under metabolic reprogramming conditions.
背景/目的:根据逆向Warburg效应,肿瘤细胞可能将乳酸作为能量来源进行代谢,并将L-乳酸转运至邻近的癌细胞、相邻的基质细胞和血管内皮细胞,从而诱导代谢重编程。肿瘤L-乳酸水平升高与转移增加、肿瘤复发及不良预后密切相关。一种可能作用于L-乳酸激活细胞的强效抗癌剂是2-甲氧基雌二醇。因此,本研究的目的是评估强效抗癌剂2-甲氧基雌二醇是否能够逆转L-乳酸诱导的骨肉瘤143B细胞的代谢重编程。
我们使用流式细胞术来确定细胞死亡、自噬、KI-67的表达、线粒体膜去极化。我们进行细胞增殖试验以确定细胞活力,并进行细胞迁移试验以确定骨肉瘤细胞的侵袭潜能。同时,使用CalcuSyn软件来评估2-甲氧基雌二醇与L-乳酸之间的相互作用。
我们证明2-甲氧基雌二醇消除了L-乳酸诱导的骨肉瘤细胞迁移和增殖。此外,我们观察到这种作用与Ki-67的调节和自噬的诱导有关。
在代谢重编程条件下,2-甲氧基雌二醇也是一种强效抗癌剂。