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The natural sweetener metabolite steviol inhibits the proliferation of human osteosarcoma U2OS cell line

机译:天然甜味剂代谢物甜菊醇抑制人骨肉瘤U2OS细胞增殖

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摘要

Steviol is the colonic metabolite of the natural sweetener steviol glycosides. It does not diffuse to the blood and the half maximal inhibitory concentration of steviol is longer compared with that of current chemotherapy agents, including 5-fluorouracil and doxorubicin. The present study demonstrated that steviol inhibits the proliferation of the human osteosarcoma U2OS cell line in a dose- and time-dependent manner, and that the inhibition rate is comparative with that of doxorubicin and 5-fluorouracil. The mechanism of this anticancer activity is also investigated. The results indicated that steviol inhibits U2OS cells through inducing G1 phase cell cycle arrest, downregulating the ability of colony formation via a mitochondrial apoptotic pathway, which was indicated by an increase of the Bax/Bcl-2 ratio and activation of cyclin-dependent kinase inhibitor 1, tumor protein 53 and cyclin-dependent kinase; whereas a Survivin and Caspase 3-independent mechanism was involved. Considering that steviol appears minimally in the plasma during metabolism, and possesses a median lethal dose of 100-fold greater compared with that of 5-fluorouracil, it may become a potential chemotherapy agent.
机译:甜菊醇是天然甜味剂甜菊醇糖苷的结肠代谢产物。它不会扩散到血液中,与包括5-氟尿嘧啶和阿霉素在内的现有化疗药物相比,甜菊醇的半数最大抑制浓度更长。本研究表明,甜菊醇以剂量和时间依赖性的方式抑制人骨肉瘤U2OS细胞的增殖,其抑制率与阿霉素和5-氟尿嘧啶相当。还研究了这种抗癌活性的机制。结果表明,甜菊醇通过诱导G1期细胞周期停滞,下调线粒体凋亡途径集落形成的能力来抑制U2OS细胞,这可以通过Bax / Bcl-2比的增加和细胞周期蛋白依赖性激酶抑制剂的激活来表明。 1,肿瘤蛋白53和细胞周期蛋白依赖性激酶;而涉及Survivin和Caspase 3独立机制。考虑到甜菊醇在新陈代谢过程中在血浆中的出现最少,并且其中位致死剂量比5-氟尿嘧啶高100倍,因此它可能成为潜在的化疗药物。

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