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体外和体内研究大麻素 1-酰基甘油对人神经胶质瘤的抗癌活性。

Anti-carcinogenic activity of anandamide on human glioma in vitro and in vivo.

机构信息

Department of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.

Department of Otorhinolaryngology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.

出版信息

Mol Med Rep. 2016 Feb;13(2):1558-62. doi: 10.3892/mmr.2015.4721. Epub 2015 Dec 28.

Abstract

The poor prognosis of gliomas is to a large extent attributed to the markedly proliferative and invasive nature of the disease. Endocannabinoids have emerged as novel potential anti-tumor agents. The present study aimed to investigate the anti-carcinogenic activity of anandamide (AEA), an endocannabinoid, on glioma cells. To assess the functional role of AEA in glioma, the effects of AEA on cell proliferation, migration, invasion, apoptosis and the cell cycle in vitro, and tumor growth in vivo, were investigated. AEA markedly inhibited the proliferation of U251 cells in a dose- and time-dependent manner. Flow cytometric assays revealed that the apoptosis rate of U251 cells upon treatment with AEA was increased. AEA also suppressed the adhesion, migration and invasion capabilities of the U251 cells. Furthermore, AEA inhibited tumor growth in vivo. These results highlighted the potential role of AEA in the tumorigenesis and progression of glioma, and suggested that AEA exhibits therapeutic potential in the management of human glioma.

摘要

神经胶质瘤的预后不良在很大程度上归因于其显著的增殖和侵袭特性。内源性大麻素已成为新的潜在抗肿瘤药物。本研究旨在研究大麻素(AEA)作为一种内源性大麻素对神经胶质瘤细胞的抗癌活性。为了评估 AEA 在神经胶质瘤中的功能作用,研究了 AEA 对体外细胞增殖、迁移、侵袭、凋亡和细胞周期以及体内肿瘤生长的影响。AEA 呈剂量和时间依赖性地显著抑制 U251 细胞的增殖。流式细胞术分析显示,AEA 处理后 U251 细胞的凋亡率增加。AEA 还抑制了 U251 细胞的黏附、迁移和侵袭能力。此外,AEA 抑制了体内肿瘤的生长。这些结果强调了 AEA 在神经胶质瘤发生和进展中的潜在作用,并表明 AEA 在人类神经胶质瘤的治疗中具有潜在的治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d9e/4732848/86e6ae8b5b02/MMR-13-02-1558-g00.jpg

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