黄根乙醇提取物对HEPG2肝癌细胞的抗癌作用

H. Yusuf, Marhami Fahriani, Cut Murzalina
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引用次数: 0

摘要

本研究旨在研究黄Arcalengisia flava (AF)根乙醇提取物对HepG2癌细胞的抗癌活性和诱导凋亡的作用。用80%乙醇浸渍法提取AF根。采用MTT法检测HepG2细胞的抗肿瘤活性和增殖能力。流式细胞术检测HepG2细胞凋亡的诱导作用。结果表明,AF乙醇提取物对HepG2细胞的IC50为109.14 μg/ml。与对照细胞相比,IC50处理下HepG2癌细胞的完整细胞(80.10±1.7%)明显减少,早期凋亡细胞(7.9±0.7%)和晚期凋亡细胞(4.9±0.35%)明显增加。此外,在作用48和72 h后,HepG2细胞的IC50(分别为77.5±5.76%和64.3±5.37%)和2xIC50(分别为75.9±1.79%和70.5±4.27%)显著下降。这项研究表明,房颤根的乙醇提取物可能用于肝癌的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ANTICANCER ACTIVITY OF ETHANOL EXTRACT OF YELLOW ROOT (Arcangelisia flava) ON HEPG2 HEPATOCELLULAR CANCER CELLS
This study aimed to evaluate anticancer activity and apoptosis induction of ethanolic extract of Arcalengisia flava (AF) roots on HepG2 cancer cell lines. The AF roots were extracted by maceration using ethanol 80%. MTT assay method was used to evaluate the anticancer activity and the proliferation of HepG2 cells. Flow cytometry method was used to assess the induction of HepG2 cells apoptosis. This study showed that the IC50 of AF ethanol extract against HepG2 cells was 109.14 μg/ml. With IC50 treatment, the apoptosis assay showed a significant decrease in intact cells (80.10±1.7%) and a significant increase in early apoptosis (7.9±0.7%) and late apoptosis cells of HepG2 cancer cells (4.9±0.35%) compared to control cells. Moreover, the proliferation of HepG2 cells was declined significantly in 48 and 72 hours after treatment with IC50 (77.5±5.76% and 64.3±5.37%, respectively) and 2xIC50 of the extract (75.9±1.79% and 70.5±4.27%, respectively). This research suggests that the ethanolic extract of AF roots can potentially be used for hepatocarcinoma treatment.
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