纯化的毛霉菌 L-天冬酰胺酶对小鼠肝癌模型和体外 Hep-G2 细胞系的治疗效果。

IF 2.8 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Dina H El-Ghonemy, Sanaa A Ali, Rehab M Abdel-Megeed, Ali M Elshafei
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引用次数: 0

摘要

背景:肝细胞癌(HCC肝细胞癌(HCC)是常见癌症之一,但难以诊断和治疗。自 20 世纪 60 年代以来,L-天冬酰胺酶已被引入小儿急性淋巴细胞白血病(ALL)的治疗方案中,并取得了良好的疗效,将存活率提高到近 90%。此外,它对实体瘤也有治疗潜力。生产不含谷氨酰胺酶的-L-天冬酰胺酶对避免谷氨酰胺酶相关毒性和过敏性很有意义。本研究从内生真菌病毒毛霉的培养滤液中纯化了不含谷氨酰胺酶的细胞外 L-天冬酰胺酶。对纯化酶的细胞毒性作用进行了评估:体外针对一组人类肿瘤细胞系,体内针对雄性威斯特白化小鼠,腹腔注射亚硝胺二乙酯(200 毫克/千克体重),然后(2 周后)口服四氯化碳(2 毫升/千克体重)。该剂量重复使用 2 个月,之后收集血液样本以估算肝肾损伤指标、血脂概况和氧化应激参数:结果:L-天冬酰胺酶从T. viride培养滤液中纯化,纯化倍数为36倍,比活度为688.1 U/mg,产率为38.9%。纯化的酶对肝癌(Hep-G2)细胞系的抗增殖活性最高,IC50为21.2 g/mL,高于对MCF-7细胞系的抗增殖活性(IC50为34.2 g/mL)。将DENA中毒组与阴性对照组进行比较,可以证明L-天冬酰胺酶调整了先前随DENA中毒而变化的肝功能酶和肝损伤标志物的水平。DENA会导致肾功能障碍,并改变血清白蛋白和肌酐水平。研究发现,服用L-天冬酰胺酶可改善测试的生物标志物水平,包括肾功能和肝功能测试。对DENA中毒组进行L-天冬酰胺酶治疗后,肝脏和肾脏组织明显改善,接近正常,与健康对照组相似:结果表明,这种纯化的T.viride L-天冬酰胺酶可能能够延缓肝癌的发展,可作为一种潜在的候选抗癌药物应用于医学领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Therapeutic impact of purified Trichoderma viride L-asparaginase in murine model of liver cancer and in vitro Hep-G2 cell line.

Therapeutic impact of purified Trichoderma viride L-asparaginase in murine model of liver cancer and in vitro Hep-G2 cell line.

Therapeutic impact of purified Trichoderma viride L-asparaginase in murine model of liver cancer and in vitro Hep-G2 cell line.

Background: Hepatocellular carcinoma (HCC) is among the common cancers, but difficult to diagnose and treat. L-asparaginase has been introduced in the treatment protocol of pediatric acute lymphoblastic leukemia (ALL) since the 1960s with a good outcome and increased survival rates to nearly 90%. Moreover, it has been found to have therapeutic potential in solid tumors. Production of glutaminase-free-L-asparaginase is of interest to avoid glutaminase-related toxicity and hypersensitivity. In the current study, an extracellular L-asparaginase that is free of L-glutaminase was purified from the culture filtrate of an endophytic fungus Trichoderma viride. The cytotoxic effect of the purified enzyme was evaluated in vitro against a panel of human tumor cell lines and in vivo against male Wister albino mice intraperitoneally injected with diethyl nitrosamine (200 mg/kg bw), followed by (after 2 weeks) oral administration of carbon tetrachloride (2 mL/kg bw). This dose was repeated for 2 months, and after that, the blood samples were collected to estimate hepatic and renal injury markers, lipid profiles, and oxidative stress parameters.

Results: L-asparaginase was purified from T. viride culture filtrate with 36 purification folds, 688.1 U/mg specific activity, and 38.9% yield. The highest antiproliferative activity of the purified enzyme was observed against the hepatocellular carcinoma (Hep-G2) cell line, with an IC50 of 21.2 g/mL, which was higher than that observed for MCF-7 (IC50 34.2 g/mL). Comparing the DENA-intoxicated group to the negative control group, it can be demonstrated that L-asparaginase adjusted the levels of the liver function enzymes and the hepatic injury markers that had previously changed with DENA intoxication. DENA causes kidney dysfunction and altered serum albumin and creatinine levels as well. Administration of L-asparaginase was found to improve the levels of the tested biomarkers including kidney and liver function tests. L-asparaginase treatment of the DENA-intoxicated group resulted in a significant improvement in the liver and kidney tissues to near normal similar to the healthy control group.

Conclusion: The results suggest that this purified T. viride L-asparaginase may be able to delay the development of liver cancer and may be used as a potential candidate for future application in medicine as an anticancer medication.

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