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西红花提取物对肺肿瘤促进和诱导细胞凋亡的抑制作用。

Suppression of pulmonary tumor promotion and induction of apoptosis by Crocus sativus L. extraction.

机构信息

Department of Physiology, School of Medicine, Mashhad University Medical Sciences, Mashhad, Iran.

出版信息

Appl Biochem Biotechnol. 2011 May;164(2):238-47. doi: 10.1007/s12010-010-9130-x. Epub 2010 Dec 12.

Abstract

Crocus sativus L., commonly known as saffron, is the raw material for one of the most expensive spice in the world, and it has been used in folk medicine for centuries. We investigated the potential of the ethanolic extract of saffron to induce cytotoxic and apoptosis effects in carcinomic human alveolar basal epithelial cells (A549), a commonly used cell culture system for in vitro studies on lung cancer. The cells were cultured in Dulbecco's modified Eagle's medium with 10% fetal bovine serum treated with different concentrations of the ethanolic extract of saffron for two consecutive days. Cell viability was quantitated by the 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay. Apoptotic cells were determined using annexin V-fluorescein isothiocyanate by flow cytometry. Saffron could decrease the cell viability in the malignant cells as a concentration- and time-dependent manner. The IC₅₀ values against the A549 cell lines were determined as 1,200 and 650 μg/ml after 24 and 48 h, respectively. Saffron-induced apoptosis of the A549 cells in a concentration-dependent manner, as determined by flow cytometry histogram of treated cells that induced apoptotic cell death, is involved in the toxicity of saffron. It might be concluded that saffron could cause cell death in the A549 cells, in which apoptosis plays an important role. Saffron could also be considered as a promising chemotherapeutic agent in lung cancer treatment in future.

摘要

藏红花,又称番红花,是世界上最昂贵的香料之一的原料,几个世纪以来一直被用于民间医学。我们研究了藏红花的乙醇提取物在诱导人肺癌细胞(A549)细胞毒性和凋亡方面的潜力,A549 细胞系是体外肺癌研究中常用的细胞培养系统。将细胞在含 10%胎牛血清的 Dulbecco 改良 Eagle 培养基中培养,并连续两天用不同浓度的藏红花乙醇提取物处理。通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法定量细胞活力。通过流式细胞术用 Annexin V-荧光素异硫氰酸酯测定凋亡细胞。藏红花可浓度和时间依赖性地降低恶性细胞中的细胞活力。24 小时和 48 小时后,对 A549 细胞系的 IC₅₀ 值分别确定为 1200 和 650 μg/ml。藏红花通过流式细胞术直方图确定以浓度依赖性方式诱导 A549 细胞凋亡,诱导细胞凋亡死亡,这与藏红花的毒性有关。可以得出结论,藏红花可能导致 A549 细胞死亡,其中凋亡起着重要作用。藏红花将来也可以被认为是治疗肺癌的有前途的化疗药物。

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