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首页> 外文期刊>International immunopharmacology >Patchouli alcohol, an essential oil of Pogostemon cablin, exhibits anti-tumorigenic activity in human colorectal cancer cells
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Patchouli alcohol, an essential oil of Pogostemon cablin, exhibits anti-tumorigenic activity in human colorectal cancer cells

机译:广cho香醇,Pogostemon cablin的精油,在人大肠癌细胞中表现出抗肿瘤活性

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Patchouli alcohol (PA) is one of the important compounds isolated from the essential oil of Pogostemon cablin (patchouli). PA has neuroprotective, anti-influenza and anti-inflammatory activities. However, anti-cancer activity of PA has not been studied so far. We performed in vitro study to investigate whether PA affects proliferation and apoptosis of human colorectal cancer cells, and to define potential molecular mechanisms. PA suppressed cell growth and induced apoptosis in a dose-dependent manner in human colorectal cancer cells (HCT116, SW480). In addition, PA decreased cell growth in MCF7, BxPC3, PC3, and HUVEC cells. Exposure of PA to HCT116 and SW480 cells activated p21 expression and suppressed the expressions of cyclin D1 and cyclin-dependent kinase 4 (CDK4) in a dose-dependent manner. In addition, PA attenuated the expressions of HDAC2 (histone deacetylase 2) and c-myc, and HDAC enzyme activity. We also observed that PA induced the transcriptional activity of NF-κB through an increase of nuclear translocation of p65. These findings suggest that PA exerts an anti-cancer activity by decreasing cell growth and increasing apoptosis in human colorectal cancer cells. The proposed mechanisms include the inhibition of HDAC2 expression and HDAC enzyme activity, and subsequent downregulation of c-myc and activation of NF-κB pathway.
机译:广cho香醇(PA)是从Pogostemon cablin(广cho香)精油中分离出的重要化合物之一。 PA具有神经保护,抗流感和抗炎活性。但是,到目前为止,尚未研究PA的抗癌活性。我们进行了体外研究,以研究PA是否会影响人类结直肠癌细胞的增殖和凋亡,并确定潜在的分子机制。 PA抑制人类结直肠癌细胞(HCT116,SW480)中的细胞生长并以剂量依赖性方式诱导细胞凋亡。此外,PA降低了MCF7,BxPC3,PC3和HUVEC细胞的细胞生长。 PA暴露于HCT116和SW480细胞可激活p21表达,并以剂量​​依赖性方式抑制cyclin D1和cyclin依赖性激酶4(CDK4)的表达。此外,PA减弱了HDAC2(组蛋白脱乙酰基酶2)和c-myc的表达以及HDAC酶的活性。我们还观察到,PA通过增加p65的核易位诱导了NF-κB的转录活性。这些发现表明PA通过降低人结肠直肠癌细胞的细胞生长和增加细胞凋亡发挥抗癌活性。提出的机制包括抑制HDAC2表达和HDAC酶活性,以及​​随后下调c-myc和激活NF-κB通路。

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