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Antitumor activity of the Ailanthus altissima bark phytochemical ailanthone against breast cancer MCF-7 cells

机译:臭椿树皮植物化学蒽酮对乳腺癌MCF-7细胞的抗肿瘤活性

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摘要

Ailanthone is isolated from the bark of Ailanthus altissima (Mill.) Swingle (Simaroubaceae). The mechanism that underlies the activity of ailanthone on MCF-7 cells was investigated by MTT assay. Breast cancer MCF-7 cells were treated with 0.5, 1.0, 2.0, 4.0 and 8.0 µg/ml ailanthone for 24, 48 and 72 h. The inhibition of proliferation induced by treatment with ailanthone was assessed by MTT assay. Apoptosis and cell cycle distribution in MCF-7 cells with the same doses of ailanthone for 48 h were determined by flow cytometry. Expression of apoptosis-associated genes and proteins were analyzed by reverse transcription-polymerase chain reaction (RT-PCR) and western blot analysis, respectively. The results revealed that ailanthone inhibited MCF-7 cell proliferation. Flow cytometry assay demonstrated that ailanthone induced apoptosis and G0/G1 cell cycle arrest in MCF-7 cells. Western blotting and RT-PCR assays demonstrated that upregulation of pro-apoptotic caspase-3 and Bcl-associated X, and downregulation of anti-apoptotic apoptosis regulator B-cell lymphoma-2 in MCF-7 cells may be associated with the induction of apoptosis and inhibition of proliferation. To the best of our knowledge, the present study is the first to investigate the antitumor activity of ailanthone from A. altissima on MCF-7 cells and to attempt to elucidate the underlying mechanism. The present study revealed the presence of ailanthone-mediated antitumor effects, indicating that ailanthone may be a novel phytomedicine with potential use in breast cancer therapy.
机译:i兰酮是从臭椿(Mil。)Swingle(Simaroubaceae)的树皮中分离出来的。通过MTT分析研究了蒽酮对MCF-7细胞的活性的机制。乳腺癌MCF-7细胞分别用0.5、1.0、2.0、4.0和8.0 µg / ml异蒽酮处理24、48和72小时。通过MTT测定评估了用蒽酮处理诱导的增殖抑制。用流式细胞仪测定相同剂量的蒽酮处理48 h后MCF-7细胞的凋亡和细胞周期分布。分别通过逆转录-聚合酶链反应(RT-PCR)和蛋白质印迹分析来分析凋亡相关基因和蛋白质的表达。结果表明,艾兰酮抑制MCF-7细胞增殖。流式细胞仪检测表明,蒽酮可诱导MCF-7细胞凋亡并抑制G0 / G1细胞周期。 Western印迹和RT-PCR分析表明MCF-7细胞中促凋亡caspase-3和Bcl相关X的上调以及抗凋亡凋亡调节剂B细胞淋巴瘤2的下调可能与诱导凋亡有关和抑制增殖。据我们所知,本研究是第一个研究拟南芥中的异蒽酮对MCF-7细胞的抗肿瘤活性并试图阐明其潜在机制。本研究揭示了艾兰酮介导的抗肿瘤作用的存在,表明艾兰酮可能是一种新型的植物药,在乳腺癌治疗中具有潜在用途。

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