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植物乳杆菌 p5 来源的精氨酸脱亚氨酶对鼠源乳腺癌细胞及非洲绿猴肾细胞的致死作用研究。

Investigation of the Lethal Effect of Purified Arginine Deiminase Purified from Lactobacillus plantarum p5 on Murine Mammary Adenocarcinoma and Vero cell Lines.

机构信息

Department of Biology, College of Sciences, Mustansiriyah University, Baghdad, Iraq.

出版信息

Arch Razi Inst. 2022 Feb 28;77(1):241-247. doi: 10.22092/ARI.2021.356587.1873. eCollection 2022 Feb.

Abstract

Cancer is one of the most serious diseases facing humanity; accordingly, it is urgent to find a cure that is rarely harmful to the patient as much as possible. It has been approved that arginine deiminase (ADI) can hydrolyze the plasma arginine to citrulline. This hydrolysis activity and reduction in the amount of intercellular arginine suppress lipopolysaccharide-induced nitric oxide synthesis. On the other hand, arginine depletion arrests the cell cycle at the G1 phase; therefore, ADI has been considered a powerful anticancer agent. The current study aimed to investigate the lethal effects of ADI purified from the p5 strain on murine mammary adenocarcinoma and Vero cell lines. Anti-proliferative activity of ADI against murine mammary adenocarcinoma) AMN3) cell line was evaluated after different incubation times (3, 6, 24, 48, and 72 h) of exposure to 1 µg/mL of ADI, compared to Vero (non-cancer cell line) transformed cell line with same conditions. The autophagy process in cancer cells was recognized after three hours of incubation with ADI which was clearly observed in the AMN3 cell line under an inverted microscope. The first stages of the programmed cell death (apoptosis) pathway were only observed in AMN3 cells after 24 h of incubation with ADI, and this process continued with the time until they reached the last stages of apoptosis after 72 h of incubation. The results of the current study showed that the AMN3 cell line was auxotrophic for arginine because it could not produce it in the presence of enzyme which had a robust activity to kill these cancer cells; however, Vero non-cancer cell line survived in the presence of ADI because it had the ability to produce arginine.

摘要

癌症是人类面临的最严重疾病之一;因此,迫切需要找到一种尽可能对患者伤害小的治疗方法。已经证实精氨酸脱亚氨酶(ADI)可以将血浆中的精氨酸水解为瓜氨酸。这种水解活性和细胞内精氨酸含量的减少抑制脂多糖诱导的一氧化氮合成。另一方面,精氨酸耗竭使细胞周期停滞在 G1 期;因此,ADI 被认为是一种强大的抗癌剂。本研究旨在研究从 p5 株中纯化的 ADI 对鼠乳腺腺癌和 Vero 细胞系的致死作用。用 1µg/ml 的 ADI 孵育不同时间(3、6、24、48 和 72 h)后,评估 ADI 对鼠乳腺腺癌(AMN3)细胞系的抗增殖活性,并与相同条件下的 Vero(非癌细胞系)转化细胞系进行比较。在用 ADI 孵育 3 小时后,在倒置显微镜下可以清楚地观察到癌细胞中的自噬过程。在用 ADI 孵育 24 h 后,仅在 AMN3 细胞中观察到程序性细胞死亡(细胞凋亡)途径的早期阶段,并且随着时间的推移,该过程一直持续到 72 h 孵育后达到细胞凋亡的最后阶段。本研究结果表明,AMN3 细胞系对精氨酸有营养依赖性,因为在存在具有强大活性的酶的情况下,它不能产生精氨酸,该酶可以杀死这些癌细胞;然而,Vero 非癌细胞系在 ADI 的存在下存活下来,因为它有能力产生精氨酸。

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