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体外鬼臼毒素对人畸胎瘤(NTERA-2)癌干样细胞的抗癌作用。

In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells.

机构信息

Institute of Biochemistry, Molecular Biology and Biotechnology, University of Colombo, 90 Cumaratunga Munidasa Mawatha, 03 Colombo, Sri Lanka.

出版信息

Biomed Res Int. 2017;2017:2413197. doi: 10.1155/2017/2413197. Epub 2017 Jun 7.

Abstract

Gedunin is one of the major compounds found in the neem tree . In the present study, antiproliferative potential of gedunin was evaluated in human embryonal carcinoma cells (NTERA-2, a cancer stem cell model) and peripheral blood mononuclear cells (PBMCs), using Sulforhodamine (SRB) and WST-1 assays, respectively. The effects of gedunin on expression of heat shock protein 90 (HSP90), its cochaperone Cdc37, and HSP client proteins (AKT, ErbB2, and HSF1) were evaluated by real-time PCR. Effects of gedunin on apoptosis were evaluated by (a) apoptosis associated morphological changes, (b) caspase 3/7 expression, (c) DNA fragmentation, (d) TUNEL assay, and (e) real-time PCR of apoptosis related genes (, and ). Gedunin showed a promising antiproliferative effect in NTERA-2 cells with IC values of 14.59, 8.49, and 6.55 g/mL at 24, 48, and 72 h after incubations, respectively, while exerting a minimal effect on PBMCs. Expression of HSP90, its client proteins, and was inhibited and and were upregulated by gedunin. Apoptosis related morphological changes, DNA fragmentation, and increased caspase 3/7 activities confirmed the proapoptotic effects of gedunin. Collectively, results indicate that gedunin may be a good drug lead for treatment of chemo and radiotherapy resistant cancer stem cells.

摘要

吉登因是从楝树中提取的主要化合物之一。本研究采用磺酰罗丹明(SRB)和 WST-1 检测法,分别在人胚胎癌细胞(NTERA-2,一种癌症干细胞模型)和外周血单个核细胞(PBMCs)中评估了吉登因的抗增殖作用。通过实时 PCR 评估了吉登因对热休克蛋白 90(HSP90)、其共伴侣 Cdc37 和 HSP 客户蛋白(AKT、ErbB2 和 HSF1)表达的影响。通过(a)凋亡相关形态变化、(b)caspase 3/7 表达、(c)DNA 片段化、(d)TUNEL 检测和(e)凋亡相关基因(、和)的实时 PCR,评估了吉登因对凋亡的影响。吉登因在 NTERA-2 细胞中表现出有希望的抗增殖作用,孵育 24、48 和 72 小时后,IC 值分别为 14.59、8.49 和 6.55μg/ml,而对 PBMCs 的作用最小。吉登因抑制 HSP90、其客户蛋白和的表达,并上调和的表达。凋亡相关形态变化、DNA 片段化和 caspase 3/7 活性增加证实了吉登因的促凋亡作用。综上所述,结果表明吉登因可能是治疗化疗和放疗耐药癌症干细胞的良好药物先导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65ea/5478822/35e62c27d1eb/BMRI2017-2413197.001.jpg

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