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亚甲二氧基黄酮类化合物:在人白血病细胞中评估细胞毒性和抗癌潜力。

Methylenedioxy flavonoids: assessment of cytotoxic and anti-cancer potential in human leukemia cells.

机构信息

Department of Pharmacy, College of Pharmacy, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul 151-742, South Korea; Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Fondation de Recherche Cancer et Sang, Hôpital Kirchberg, 9 Rue Edward Steichen, 2540 Luxembourg, Luxembourg.

Department of Chemistry & QOPNA, University of Aveiro, 3810-193 Aveiro, Portugal; Department of Chemistry, Goa University, Taleigao Plateau, Goa 403 206, India.

出版信息

Eur J Med Chem. 2014 Sep 12;84:173-80. doi: 10.1016/j.ejmech.2014.07.003. Epub 2014 Jul 3.

Abstract

A new series of chalcones, flavanones and flavones with methylenedioxy group at the 3',4' position in chalcone, 7,8 position in flavanones and flavones with mono-, di- and trimethoxy groups in the benzaldehyde ring have been assessed for their effect on proliferation, cytotoxic potential and apoptosis in human leukemia cells. Among the tested compounds, the chalcone series showed the best activity and chalcone 3 (mono methoxy group at the ortho position in A-ring) showed a significant effect on down-regulation of cancer cell proliferation and viability in three different leukemia cell lines (K562, Jurkat, U937). The executioner caspase cleavage analyses indicated that the cytotoxic effect mediated by chalcone 3 is due to induction of apoptotic cell death. Interestingly, the cytotoxic effect was cell type-specific and targeted preferentially cancer cells as peripheral blood mononuclear cells (PBMCs) from healthy donors were less affected by the treatment compared to K562, Jurkat and U937 leukemia cells. Altogether our results indicate a potential drug candidate with interesting differential toxicity obeying Lipinski's rule of five.

摘要

已评估了一系列具有 3',4'位甲叉基的查耳酮、7,8 位甲叉基的黄烷酮和黄酮以及苯甲醛环中单、二和三甲氧基的新查耳酮、黄烷酮和黄酮,以研究它们对人白血病细胞增殖、细胞毒性潜力和细胞凋亡的影响。在所测试的化合物中,查耳酮系列表现出最佳的活性,查耳酮 3(A 环邻位单甲氧基)对三种不同白血病细胞系(K562、Jurkat、U937)中癌细胞增殖和活力的下调有显著作用。效应半胱氨酸蛋白酶切割分析表明,查耳酮 3 介导的细胞毒性作用是由于诱导细胞凋亡性死亡。有趣的是,细胞毒性作用具有细胞类型特异性,并且优先靶向癌细胞,因为与 K562、Jurkat 和 U937 白血病细胞相比,来自健康供体的外周血单核细胞(PBMCs)受治疗的影响较小。总的来说,我们的结果表明,具有 5 个 Lipinski 规则的有趣差异毒性的潜在候选药物。

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