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从枳壳果实中分离出的一种新型三萜类化合物25-甲氧基异风车子素A介导人肝癌细胞的生长抑制和G1期细胞周期阻滞。

Growth inhibition and G1 cell cycle arrest mediated by 25-methoxyhispidol A, a novel triterpenoid, isolated from the fruit of Poncirus trifoliata in human hepatocellular carcinoma cells.

作者信息

Hong Ji- Young, Min Hye-Young, Xu Guang Hua, Lee Jong-Gu, Lee Seung-Ho, Kim Young Shik, Kang Sam Sik, Lee Sang Kook

机构信息

College of Pharmacy, Ewha Womans University, Seoul, Korea.

出版信息

Planta Med. 2008 Feb;74(2):151-5. doi: 10.1055/s-2008-1034286. Epub 2008 Jan 24.

Abstract

Poncirus trifoliata (Rutaceae) extracts have been known to possess anti-allergic, anti-inflammatory and antiviral activities. However, other biological activities, especially, the anticancer potential of extracts of P. trifoliata or its constituents, have not been fully investigated yet. In this study, we have evaluated the antiproliferative effects of a novel triterpenoid, 25-methoxyhispidol A, isolated from the fruit of P. trifoliata against SK-HEP-1 human hepatocellular carcinoma cells. Flow cytometric analysis indicated that 25-methoxyhispidol A arrests the cell cycle in the G1 phase at the earlier time and subsequently induces apoptosis of the cancer cells. Further study revealed that the cell cycle arrest in the G1 phase by 25-methoxyhispidol A correlated well with the inhibition of phosphorylation of the retinoblastoma (Rb) protein, and with the down-regulation of cyclin D1 and cyclin-dependent kinase cdk4 and the induction of cdk inhibitor p21 (WAF1/Cip1) protein. These findings suggest the potential of 25-methoxyhispidol A isolated from the fructus of P. trifoliata as an antitumor agent against human hepatocarcinoma cells by arresting the cell cycle and inducing apoptosis.

摘要

已知枳(芸香科)提取物具有抗过敏、抗炎和抗病毒活性。然而,其他生物活性,尤其是枳提取物或其成分的抗癌潜力,尚未得到充分研究。在本研究中,我们评估了从枳果实中分离出的一种新型三萜类化合物25-甲氧基刺桐醇A对SK-HEP-1人肝癌细胞的抗增殖作用。流式细胞术分析表明,25-甲氧基刺桐醇A在早期将细胞周期阻滞在G1期,随后诱导癌细胞凋亡。进一步研究发现,25-甲氧基刺桐醇A使细胞周期阻滞在G1期与抑制视网膜母细胞瘤(Rb)蛋白磷酸化、下调细胞周期蛋白D1和细胞周期蛋白依赖性激酶cdk4以及诱导cdk抑制剂p21(WAF1/Cip1)蛋白密切相关。这些发现表明,从枳果实中分离出的25-甲氧基刺桐醇A具有通过阻滞细胞周期和诱导凋亡来对抗人肝癌细胞的抗肿瘤药物潜力。

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