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漆树乙醇提取物通过上调p27Kip1抑制AGS胃癌细胞的细胞周期进程并诱导凋亡。

Inhibition of cell cycle progression via p27Kip1 upregulation and apoptosis induction by an ethanol extract of Rhus verniciflua Stokes in AGS gastric cancer cells.

作者信息

Kim Ji Hye, Kim Hwang-Phill, Jung Chang-Hwa, Hong Myung Hee, Hong Mu-Chang, Bae Hyun-Su, Lee Sun-Dong, Park Seon-Yeong, Park Jong-Hyeong, Ko Seong-Gyu

机构信息

Clinical Biology and Pharmacogenomics Laboratory, College of Oriental Medicine, Kyunghee University, Seoul 130-701, South Korea.

出版信息

Int J Mol Med. 2006 Jul;18(1):201-8.

Abstract

Botanical preparations are widely used by patient with cancer in Korea, Japan and China. Rhus verniciflua Stokes (RVS) has traditionally been used as a medicinal ingredient for the therapy of stomach and uterine cancer. In this study, we showed that exposure to an ethanol extract of RVS (50 microg/ml) resulted in a synergistic inhibitory effect on cell growth in AGS cells. Growth inhibition was related with the inhibition of proliferation and induction of apoptosis. The extract induces G1-cell cycle arrest through the regulation of cyclins, the induction of p27Kip1, and decrease the CDK2 kinase activity. The upregulated p27Kip1 level is caused by protein stability increment by the reduction of Skp2, a key molecule related with p27Kip1 ubiquitination and degradation, and de novo protein synthesis. RVS extract induces apoptosis through the expression of Bax, poly(ADP-ribose) polymerase (PARP) and activation of caspase-3. RVS extract induces G1-cell cycle arrest via accumulation of p27Kip1 controlled by Skp2 reduction and apoptosis passing through an intrinsic pathway in human gastric cancer cells but not in normal cells, therefore we suggest that this extract could be a candidate medicine or compound for the development of novel class of anti-cancer drugs.

摘要

植物制剂在韩国、日本和中国被癌症患者广泛使用。漆树(RVS)传统上一直被用作治疗胃癌和子宫癌的药用成分。在本研究中,我们发现,AGS细胞暴露于RVS乙醇提取物(50微克/毫升)会对细胞生长产生协同抑制作用。生长抑制与增殖抑制和细胞凋亡诱导有关。该提取物通过调节细胞周期蛋白、诱导p27Kip1以及降低CDK2激酶活性来诱导G1期细胞周期停滞。p27Kip1水平上调是由于Skp2减少导致蛋白质稳定性增加,Skp2是与p27Kip1泛素化和降解相关的关键分子,同时也由于从头合成蛋白质。RVS提取物通过Bax、聚(ADP - 核糖)聚合酶(PARP)的表达和半胱天冬酶 - 3的激活诱导细胞凋亡。RVS提取物通过Skp2减少控制的p27Kip1积累在人胃癌细胞中诱导G1期细胞周期停滞,并通过内在途径诱导细胞凋亡,但在正常细胞中不诱导,因此我们认为这种提取物可能是开发新型抗癌药物的候选药物或化合物。

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