Department of Medical Biochemistry, Faculty of Medicine in Hradec Kralove, Charles University, Simkova 870, 500 03 Hradec Kralove, Czech Republic.
Department of Biological and Biochemical Sciences, Faculty of Chemical Technology, University of Pardubice, Studentska 573, 532 10 Pardubice, Czech Republic.
Int J Mol Sci. 2021 Jun 29;22(13):7014. doi: 10.3390/ijms22137014.
Pancracine, a montanine-type Amaryllidaceae alkaloid (AA), is one of the most potent compounds among natural isoquinolines. In previous studies, pancracine exhibited cytotoxic activity against diverse human cancer cell lines in vitro. However, further insight into the molecular mechanisms that underlie the cytotoxic effect of pancracine have not been reported and remain unknown. To fill this void, the cell proliferation and viability of cancer cells was explored using the Trypan Blue assay or by using the xCELLigence system. The impact on the cell cycle was determined by flow cytometry. Apoptosis was evaluated by Annexin V/PI and by quantifying the activity of caspases (-3/7, -8, and -9). Proteins triggering growth arrest or apoptosis were detected by Western blotting. Pancracine has strong antiproliferative activity on A549 cells, lasting up to 96 h, and antiproliferative and cytotoxic effects on MOLT-4 cells. The apoptosis-inducing activity of pancracine in MOLT-4 cells was evidenced by the significantly higher activity of caspases. This was transmitted through the upregulation of p53 phosphorylated on Ser392, p38 MAPK phosphorylated on Thr180/Tyr182, and upregulation of p27. The pancracine treatment negatively altered the proliferation of A549 cells as a consequence of an increase in G1-phase accumulation, associated with the downregulation of Rb phosphorylated on Ser807/811 and with the concomitant upregulation of p27 and downregulation of Akt phosphorylated on Thr308. This was the first study to glean a deeper mechanistic understanding of pancracine activity in vitro. Perturbation of the cell cycle and induction of apoptotic cell death were considered key mechanisms of pancracine action.
苦藏春碱是一种茄科藜芦生物碱(AA),是天然异喹啉类中最有效的化合物之一。在以前的研究中,苦藏春碱在体外对多种人类癌细胞系表现出细胞毒性活性。然而,对于苦藏春碱细胞毒性作用的分子机制的进一步深入了解尚未报道,目前仍不清楚。为了填补这一空白,使用台盼蓝检测法或 xCELLigence 系统来研究癌细胞的细胞增殖和活力。通过流式细胞术确定对细胞周期的影响。通过 Annexin V/PI 评估细胞凋亡,并定量测定半胱天冬酶(-3/7、-8 和 -9)的活性。通过 Western blot 检测触发生长停滞或凋亡的蛋白质。苦藏春碱对 A549 细胞具有很强的增殖抑制活性,持续长达 96 小时,对 MOLT-4 细胞具有增殖抑制和细胞毒性作用。在 MOLT-4 细胞中,苦藏春碱诱导细胞凋亡的活性通过 caspase 活性的显著升高得到证实。这是通过上调磷酸化丝氨酸 392 上的 p53、磷酸化苏氨酸 180/酪氨酸 182 上的 p38 MAPK 和上调 p27 来传递的。苦藏春碱处理通过增加 G1 期积累,导致 Rb 磷酸化丝氨酸 807/811 下调,同时 p27 上调和 Akt 磷酸化苏氨酸 308 下调,对 A549 细胞的增殖产生负面影响。这是首次深入了解苦藏春碱在体外的作用机制的研究。扰乱细胞周期和诱导细胞凋亡被认为是苦藏春碱作用的关键机制。