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去甲斑蝥素诱导 HL-60 细胞凋亡的体外研究。

Norcantharidin Induces HL-60 Cells Apoptosis In Vitro.

机构信息

School of Pre-Clinical Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.

出版信息

Evid Based Complement Alternat Med. 2012;2012:154271. doi: 10.1155/2012/154271. Epub 2012 Jun 24.

DOI:10.1155/2012/154271
PMID:22778770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3388623/
Abstract

Norcantharidin (NCTD) is the demethylated form of cantharidin, which is the active substance of mylabris, and is known to have anticancer potentials. The aim of this paper was to assess the apoptosis-inducing effect of NCTD on HL-60 cells. Methods. The effects of NCTD were detected by flow cytometer on the cell toxicity, cell cycle, and apoptosis of HL-60 cells cultured in vitro. Results. After 48-hour treatment with NCTD, the growth of HL-60 cells was inhibited significantly. The summit of apoptosis appeared after 24 hours. The percentage of the cells in G(1) phase decreased and then increased in S and G(2)+ M phase, while the S and G(2)+ M phases were blocked after treatment with 5, 10, and 50 μmol/L NCTD for 24 hours. Conclusions. NCTD can induce the apoptosis of HL-60 cells and inhibit the fissiparism, and the domino effect was obviously correlated with the time and dosage.

摘要

去甲斑蝥素(NCTD)是斑蝥素的去甲基化形式,是斑蝥的活性物质,已知具有抗癌潜力。本文旨在评估 NCTD 对 HL-60 细胞的诱导凋亡作用。方法。通过流式细胞仪检测 NCTD 对体外培养的 HL-60 细胞的细胞毒性、细胞周期和凋亡的影响。结果。NCTD 处理 48 小时后,HL-60 细胞的生长明显受到抑制。凋亡的高峰出现在 24 小时后。细胞在 G1 期的百分比减少,然后在 S 和 G2+M 期增加,而用 5、10 和 50μmol/L NCTD 处理 24 小时后,S 和 G2+M 期被阻断。结论。NCTD 可诱导 HL-60 细胞凋亡,抑制分裂,多米诺骨牌效应与时间和剂量明显相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/bd771ea5181a/ECAM2012-154271.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/2ba6f2063a9c/ECAM2012-154271.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/b38a35ca6bfd/ECAM2012-154271.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/576986185902/ECAM2012-154271.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/bd771ea5181a/ECAM2012-154271.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/2ba6f2063a9c/ECAM2012-154271.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/b38a35ca6bfd/ECAM2012-154271.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/576986185902/ECAM2012-154271.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/3388623/bd771ea5181a/ECAM2012-154271.004.jpg

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本文引用的文献

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Norcantharidin preferentially induces apoptosis in human leukemic Jurkat cells without affecting viability of normal blood mononuclear cells.去甲斑蝥素优先诱导人白血病Jurkat细胞凋亡,而不影响正常血液单核细胞的活力。
Food Chem Toxicol. 2007 Sep;45(9):1678-87. doi: 10.1016/j.fct.2007.03.003. Epub 2007 Mar 12.
2
Norcantharidin inhibits DNA replication and induces apoptosis with the cleavage of initiation protein Cdc6 in HL-60 cells.去甲斑蝥素抑制HL-60细胞中的DNA复制,并通过起始蛋白Cdc6的裂解诱导细胞凋亡。
Anticancer Drugs. 2006 Mar;17(3):307-14. doi: 10.1097/00001813-200603000-00009.
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Effect of norcantharidin on proliferation and invasion of human gallbladder carcinoma GBC-SD cells.
去甲斑蝥素对人系膜细胞增殖、凋亡及细胞周期的影响。
Ren Fail. 2017 Nov;39(1):458-464. doi: 10.1080/0886022X.2017.1308257.
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Intraarterial administration of norcantharidin attenuates ischemic stroke damage in rodents when given at the time of reperfusion: novel uses of endovascular capabilities.在再灌注时给予腔内诺卡他林可减轻啮齿动物缺血性中风损伤:血管内能力的新用途。
J Neurosurg. 2016 Jul;125(1):152-9. doi: 10.3171/2015.4.JNS142400. Epub 2015 Nov 6.
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Norcantharidin inhibits Wnt signal pathway via promoter demethylation of WIF-1 in human non-small cell lung cancer.去甲斑蝥素通过人非小细胞肺癌中WIF-1启动子去甲基化抑制Wnt信号通路。
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The Synthetic Compound Norcantharidin Induced Apoptosis in Mantle Cell Lymphoma In Vivo and In Vitro through the PI3K-Akt-NF- κ B Signaling Pathway.合成化合物去甲斑蝥素通过 PI3K-Akt-NF-κB 信号通路诱导体内外套细胞淋巴瘤细胞凋亡。
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