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黄连,一种中国草药提取物,通过抑制细胞周期蛋白B1的表达和抑制人癌细胞中的细胞周期蛋白依赖性激酶2(CDC2)活性来抑制细胞生长。

Huanglian, A chinese herbal extract, inhibits cell growth by suppressing the expression of cyclin B1 and inhibiting CDC2 kinase activity in human cancer cells.

作者信息

Li X K, Motwani M, Tong W, Bornmann W, Schwartz G K

机构信息

Gastrointestinal Oncology Research Laboratory for New Drug Development, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.

出版信息

Mol Pharmacol. 2000 Dec;58(6):1287-93. doi: 10.1124/mol.58.6.1287.

Abstract

Huanglian is an herb that is widely used in China for the treatment of gastroenteritis. We elected to determine whether huanglian could inhibit tumor cell growth by modulating molecular events directly associated with the cell cycle. Huanglian inhibited tumor growth and colony formation of gastric, colon, and breast cancer cell lines in a time- and dose-dependent manner. Cell growth was completely inhibited after 3 days of continuous drug exposure to 10 microg/ml of herb. This degree of growth inhibition was significantly greater than that observed with berberine, the major constituent of the herb. The inhibition of cell growth by huanglian was associated with up to 8-fold suppression of cyclin B1 protein. This resulted in complete inhibition of cdc2 kinase activity and accumulation of cells in G(2). The mRNA expression of cyclin B1 was not changed after huanglian treatment. There was no change in the protein expression of cyclins A or E. Therefore, the effect of huanglian on inhibiting tumor growth seems to be mediated by the selective suppression of cyclin B1, which results in the inhibition of cdc2 kinase activity. Inhibition of cyclin dependent kinase (cdk) activity is emerging as an attractive target for cancer chemotherapy. Huanglian represents a class of agents that can inhibit tumor cell growth by directly suppressing the expression of a cyclin subunit that is critical for cell cycle progression. These results indicate that traditional Chinese herbs may represent a new source of agents designed for selective inhibition of cyclin dependent kinases in cancer therapy.

摘要

黄连是一种在中国广泛用于治疗肠胃炎的草药。我们决定确定黄连是否能通过调节与细胞周期直接相关的分子事件来抑制肿瘤细胞生长。黄连以时间和剂量依赖性方式抑制胃癌、结肠癌和乳腺癌细胞系的肿瘤生长和集落形成。连续3天将药物暴露于10微克/毫升的草药后,细胞生长被完全抑制。这种生长抑制程度明显大于该草药的主要成分黄连素所观察到的程度。黄连对细胞生长的抑制与细胞周期蛋白B1蛋白高达8倍的抑制有关。这导致cdc2激酶活性完全被抑制,细胞在G(2)期积累。黄连处理后细胞周期蛋白B1的mRNA表达没有变化。细胞周期蛋白A或E的蛋白表达没有改变。因此,黄连抑制肿瘤生长的作用似乎是通过选择性抑制细胞周期蛋白B1介导的,这导致cdc2激酶活性受到抑制。抑制细胞周期蛋白依赖性激酶(cdk)活性正在成为癌症化疗的一个有吸引力的靶点。黄连代表了一类能够通过直接抑制对细胞周期进程至关重要的细胞周期蛋白亚基的表达来抑制肿瘤细胞生长的药物。这些结果表明,传统中药可能代表了一类用于癌症治疗中选择性抑制细胞周期蛋白依赖性激酶的新型药物来源。

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