Department of Biological and Environmental Sciences, School of Arts and Sciences, Beirut Arab University, Beirut, Lebanon.
Department of Natural Sciences, School of Arts and Sciences, Lebanese American University, Beirut, 1102 2801, Lebanon.
Hum Cell. 2021 Jan;34(1):152-164. doi: 10.1007/s13577-020-00437-4. Epub 2020 Sep 26.
Deregulating cellular energetics by reprogramming metabolic pathways, including arginine metabolism, is critical for cancer cell onset and survival. Drugs that target the specific metabolic requirements of cancer cells have emerged as promising targeted cancer therapeutics. In this study, we investigate the therapeutic potential of targeting colon cancer cells using arginine deprivation induced by a pegylated cobalt-substituted recombinant human Arginase I [HuArgI (Co)-PEG5000]. Four colon cancer cell lines were tested for their sensitivity to [HuArgI (Co)-PEG5000] as well as for their mechanism of cell death following arginine deprivation. All four cell lines were sensitive to arginine deprivation induced by [HuArgI (Co)-PEG5000]. All cells expressed ASS1 and were rescued from arginine deprivation-induced cytotoxicity by the addition of excess L-citrulline, indicating they are partially auxotrophic for arginine. Mechanistically, cells treated with [HuArgI (Co)-PEG5000] were negative for AnnexinV and lacked caspase activation. Further investigation revealed that arginine deprivation leads to a marked and prolonged activation of autophagy in both Caco-2 and T84 cell lines. Finally, we show that [HuArgI (Co)-PEG5000] causes cell death by sustained activation of autophagy as evidenced by the decrease in cell cytotoxicity upon treatment with chloroquine, an autophagy inhibitor. Altogether, these data demonstrate that colon cancer cells are partially auxotrophic for arginine and sensitive to [HuArgI (Co)-PEG5000]-induced arginine deprivation. They also show that the activation of autophagy does not play protective roles but rather, induces cytotoxicity and leads to cell death.
通过重新编程代谢途径(包括精氨酸代谢)来调节细胞能量,这对癌细胞的发生和存活至关重要。针对癌细胞特定代谢需求的药物已成为有前途的靶向癌症治疗药物。在这项研究中,我们研究了使用聚乙二醇化钴取代的重组人精氨酸酶 I [HuArgI(Co)-PEG5000]诱导的精氨酸剥夺靶向结肠癌细胞的治疗潜力。测试了四种结肠癌细胞系对 [HuArgI(Co)-PEG5000]的敏感性,以及在精氨酸剥夺后细胞死亡的机制。所有四种细胞系对 [HuArgI(Co)-PEG5000]诱导的精氨酸剥夺均敏感。所有细胞均表达 ASS1,并通过添加过量的 L-瓜氨酸从精氨酸剥夺诱导的细胞毒性中得到挽救,表明它们对精氨酸部分是营养缺陷型的。从机制上讲,用 [HuArgI(Co)-PEG5000]处理的细胞 AnnexinV 呈阴性,并且缺乏 caspase 激活。进一步的研究表明,精氨酸剥夺会导致 Caco-2 和 T84 细胞系中自噬的明显和持久激活。最后,我们表明,[HuArgI(Co)-PEG5000]通过持续激活自噬引起细胞死亡,这可以通过在用自噬抑制剂氯喹处理时降低细胞细胞毒性来证明。总而言之,这些数据表明结肠癌细胞对精氨酸部分是营养缺陷型的,并且对 [HuArgI(Co)-PEG5000]诱导的精氨酸剥夺敏感。它们还表明,自噬的激活没有起到保护作用,而是诱导细胞毒性并导致细胞死亡。