Suppr超能文献

小檗碱的兴奋效应减弱了化疗药物的抗癌活性。

Hormetic Effect of Berberine Attenuates the Anticancer Activity of Chemotherapeutic Agents.

作者信息

Bao Jiaolin, Huang Borong, Zou Lidi, Chen Shenghui, Zhang Chao, Zhang Yulin, Chen Meiwan, Wan Jian-Bo, Su Huanxing, Wang Yitao, He Chengwei

机构信息

State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Taipa, Macao, China.

Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

PLoS One. 2015 Sep 30;10(9):e0139298. doi: 10.1371/journal.pone.0139298. eCollection 2015.

Abstract

Hormesis is a phenomenon of biphasic dose response characterized by exhibiting stimulatory or beneficial effects at low doses and inhibitory or toxic effects at high doses. Increasing numbers of chemicals of various types have been shown to induce apparent hormetic effect on cancer cells. However, the underlying significance and mechanisms remain to be elucidated. Berberine, one of the major active components of Rhizoma coptidis, has been manifested with notable anticancer activities. This study aims to investigate the hormetic effect of berberine and its influence on the anticancer activities of chemotherapeutic agents. Our results demonstrated that berberine at low dose range (1.25 ~ 5 μM) promoted cell proliferation to 112% ~170% of the untreated control in various cancer cells, while berberine at high dose rage (10 ~ 80 μM) inhibited cell proliferation. Further, we observed that co-treatment with low dose berberine could significantly attenuate the anticancer activity of chemotherapeutic agents, including fluorouracil (5-FU), camptothecin (CPT), and paclitaxel (TAX). The hormetic effect and thereby the attenuated anticancer activity of chemotherapeutic drugs by berberine may attributable to the activated protective stress response in cancer cells triggered by berberine, as evidenced by up-regulated MAPK/ERK1/2 and PI3K/AKT signaling pathways. These results provided important information to understand the potential side effects of hormesis, and suggested cautious application of natural compounds and relevant herbs in adjuvant treatment of cancer.

摘要

兴奋效应是一种双相剂量反应现象,其特征是在低剂量时表现出刺激或有益作用,而在高剂量时表现出抑制或毒性作用。越来越多的各类化学物质已被证明可对癌细胞产生明显的兴奋效应。然而,其潜在意义和机制仍有待阐明。黄连素是黄连的主要活性成分之一,已表现出显著的抗癌活性。本研究旨在探讨黄连素的兴奋效应及其对化疗药物抗癌活性的影响。我们的结果表明,低剂量范围(1.255μM)的黄连素可使各种癌细胞的细胞增殖促进至未处理对照的112%170%,而高剂量范围(10~80μM)的黄连素则抑制细胞增殖。此外,我们观察到低剂量黄连素联合处理可显著减弱包括氟尿嘧啶(5-FU)、喜树碱(CPT)和紫杉醇(TAX)在内的化疗药物的抗癌活性。黄连素的兴奋效应以及由此导致的化疗药物抗癌活性减弱可能归因于黄连素触发的癌细胞中激活的保护性应激反应,丝裂原活化蛋白激酶/细胞外信号调节激酶1/2(MAPK/ERK1/2)和磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/AKT)信号通路的上调证明了这一点。这些结果为理解兴奋效应的潜在副作用提供了重要信息,并建议在癌症辅助治疗中谨慎应用天然化合物和相关草药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d913/4589364/53122f889a87/pone.0139298.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验