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α-常春藤皂苷对乳腺癌细胞的抗癌作用及机制

The anticancer effect and mechanism of α-hederin on breast cancer cells.

作者信息

Cheng Lin, Xia Tian-Song, Wang Yi-Fen, Zhou Wenbin, Liang Xiu-Qing, Xue Jin-Qiu, Shi Liang, Wang Ying, Ding Qiang, Wang Minhai

机构信息

Jiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing 210029, P.R. China.

State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650204, P.R. China.

出版信息

Int J Oncol. 2014 Aug;45(2):757-63. doi: 10.3892/ijo.2014.2449. Epub 2014 May 19.

Abstract

Natural plant products occupy a very important position in the area of cancer chemotherapy. Many triterpenoid saponins have been proved as potential agents for chemoprevention and therapy of breast cancer. α-hederin, a monodesmosidic triterpenoid saponin distributed in Hedera or Nigella species, displays many biological activities. It is increasingly investigated for its promising anticancer potential since it has been shown to have cytotoxicity against several types of cancer cells. However, studies of α-hederin on breast cancer are limited, most of which focus on biological activity, while the mechanisms have not been widely reported yet. Previously, we purified and identified α-hederin from Clematis ganpiniana, a herb used in traditional Chinese medicine with antitumor action. In the present study, α-hederin showed strong inhibitory activity on the growth of breast cancer cells and induced apoptosis in these cells. α-hederin induced depolarization of mitochondrial membrane potential which released Apaf-1 and cytochrome c from the intermembrane space into the cytosol, where they promoted caspase-3 and caspase-9 activation. This is the first report on the growth inhibition and pro-apoptotic effects of α-hederin on breast cancer cells and the relative apoptosis pathways. It implied that triterpenoid saponin α-hederin could be a promising candidate for chemotherapy of breast cancer.

摘要

天然植物产品在癌症化疗领域占据非常重要的地位。许多三萜皂苷已被证明是乳腺癌化学预防和治疗的潜在药物。α-常春藤皂苷,一种分布于常春藤属或黑种草属植物中的单糖链三萜皂苷,具有多种生物活性。由于它已被证明对几种类型的癌细胞具有细胞毒性,其有前景的抗癌潜力正受到越来越多的研究。然而,关于α-常春藤皂苷对乳腺癌的研究有限,其中大多数集中在生物活性方面,而其作用机制尚未有广泛报道。此前,我们从中国传统抗肿瘤草药甘青铁线莲中纯化并鉴定出了α-常春藤皂苷。在本研究中,α-常春藤皂苷对乳腺癌细胞的生长表现出强烈的抑制活性,并诱导这些细胞凋亡。α-常春藤皂苷诱导线粒体膜电位去极化,使凋亡蛋白酶激活因子-1和细胞色素c从膜间隙释放到细胞质中,在那里它们促进了半胱天冬酶-3和半胱天冬酶-9的激活。这是关于α-常春藤皂苷对乳腺癌细胞的生长抑制和促凋亡作用以及相关凋亡途径的首次报道。这意味着三萜皂苷α-常春藤皂苷可能是乳腺癌化疗的一个有前景的候选药物。

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