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Cucurbitacins - a promising target for cancer therapy.葫芦素——癌症治疗的一个有前景的靶点。
Int J Health Sci (Qassim). 2013 Jan;7(1):77-89. doi: 10.12816/0006025.
2
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Biological activities and potential molecular targets of cucurbitacins: a focus on cancer.葫芦素的生物活性及潜在分子靶点:以癌症为重点。
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本文引用的文献

1
Biological activities and potential molecular targets of cucurbitacins: a focus on cancer.葫芦素的生物活性及潜在分子靶点:以癌症为重点。
Anticancer Drugs. 2012 Sep;23(8):777-87. doi: 10.1097/CAD.0b013e3283541384.
2
Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives.二氢葫芦素 B 和葫芦素 B 衍生物的合成及细胞毒性活性评价。
Bioorg Med Chem. 2012 May 1;20(9):3016-30. doi: 10.1016/j.bmc.2012.03.001. Epub 2012 Mar 15.
3
Cucurbitacins as inducers of cell death and a rich source of potential anticancer compounds.葫芦素作为细胞死亡的诱导剂和潜在抗癌化合物的丰富来源。
Curr Pharm Des. 2012;18(12):1663-76. doi: 10.2174/138161212799958549.
4
In vitro and in vivo study of cucurbitacins-type triterpene glucoside from Citrullus colocynthis growing in Saudi Arabia against hepatocellular carcinoma.在沙特阿拉伯生长的苦瓜中的葫芦素型三萜糖苷的体外和体内研究对肝癌的作用。
Environ Toxicol Pharmacol. 2012 Mar;33(2):245-51. doi: 10.1016/j.etap.2011.12.010. Epub 2011 Dec 16.
5
Isolation, structure elucidation, and biological evaluation of 16,23-epoxycucurbitacin constituents from Eleaocarpus chinensis.从海枣(Eleaocarpus chinensis)中分离、结构鉴定和生物评价 16,23-环氧葫芦素成分。
J Nat Prod. 2012 Mar 23;75(3):444-52. doi: 10.1021/np200879p. Epub 2012 Jan 12.
6
Effects of cucurbitacins on cell morphology are associated with sensitization of renal carcinoma cells to TRAIL-induced apoptosis.葫芦素对细胞形态的影响与增强肾癌细胞对 TRAIL 诱导凋亡的敏感性有关。
Apoptosis. 2012 Jan;17(1):79-89. doi: 10.1007/s10495-011-0652-7.
7
Inhibition of Wnt signaling by cucurbitacin B in breast cancer cells: reduction of Wnt-associated proteins and reduced translocation of galectin-3-mediated β-catenin to the nucleus.葫芦素 B 抑制乳腺癌细胞中的 Wnt 信号通路:减少 Wnt 相关蛋白,降低半乳糖凝集素-3 介导的β-连环蛋白向核内易位。
J Cell Biochem. 2012 Jan;113(1):49-60. doi: 10.1002/jcb.23326.
8
Apoptosis induction through proteasome inhibitory activity of cucurbitacin D in human T-cell leukemia.葫芦素 D 通过蛋白酶体抑制活性诱导人 T 细胞白血病细胞凋亡。
Cancer. 2011 Jun 15;117(12):2735-46. doi: 10.1002/cncr.25711. Epub 2010 Dec 23.
9
Cucurbitacin B has a potent antiproliferative effect on breast cancer cells in vitro and in vivo.葫芦素B在体外和体内对乳腺癌细胞均具有强大的抗增殖作用。
Cancer Sci. 2008 Sep;99(9):1793-7. doi: 10.1111/j.1349-7006.2008.00899.x. Epub 2008 Jul 10.
10
Activated kRas protects colon cancer cells from cucurbitacin-induced apoptosis: the role of p53 and p21.激活的kRas保护结肠癌细胞免受葫芦素诱导的凋亡:p53和p21的作用。
Biochem Pharmacol. 2008 Jul 15;76(2):198-207. doi: 10.1016/j.bcp.2008.05.004. Epub 2008 May 8.

葫芦素——癌症治疗的一个有前景的靶点。

Cucurbitacins - a promising target for cancer therapy.

作者信息

Alghasham Abdullah A

机构信息

College of Medicine, Qassim University, Kingdom of Saudi Arabia.

出版信息

Int J Health Sci (Qassim). 2013 Jan;7(1):77-89. doi: 10.12816/0006025.

DOI:10.12816/0006025
PMID:23559908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3612419/
Abstract

During the last decades a large number of cucurbitacins have been isolated from various plant species belonging to other plant families than Cucurbitaceae. Although the roots and the fruits of plant belong to these Cucurbitaceae species are very bitter, they have been used as folk medicines in some countries because of their wide spectrum of pharmacological activities such as anti-inflammation and anticancer effects. In the last ten years, cucurbitacins had been shown to inhibit proliferation and induced apoptosis utilizing a long array of in vitro and in vivo cancer cell models. Several molecular targets for cucurbitacins have been discovered, such as fibrous-actin, signal transducer and activator of transcription (STAT), cyclooxygenase-2, etc. This review aimed at elucidating the natural sources of some cucurbitacin compounds, their chemical structure and derivatives, physical properties, biological activities and mechanism by which they reduce the proliferation human cancer cells. This widens our armaments against a devastating disease that we are failing to face.

摘要

在过去几十年里,人们从葫芦科以外的其他植物科的各种植物物种中分离出了大量的葫芦素。尽管这些葫芦科植物的根和果实非常苦,但由于它们具有广泛的药理活性,如抗炎和抗癌作用,在一些国家已被用作民间药物。在过去十年中,利用一系列体外和体内癌细胞模型,已证明葫芦素能抑制增殖并诱导凋亡。已经发现了葫芦素的几个分子靶点,如纤维肌动蛋白、信号转导和转录激活因子(STAT)、环氧化酶-2等。本综述旨在阐明一些葫芦素化合物的天然来源、它们的化学结构和衍生物、物理性质、生物活性以及它们减少人类癌细胞增殖的机制。这拓宽了我们对抗一种我们未能面对的毁灭性疾病的武器库。