Suppr超能文献

槲寄生凝集素通过使Akt去磷酸化诱导人A253癌细胞凋亡并抑制端粒酶。

Mistletoe lectin induces apoptosis and telomerase inhibition in human A253 cancer cells through dephosphorylation of Akt.

作者信息

Choi Sang Ho, Lyu Su Yun, Park Won Bong

机构信息

Brain Disease Research Center, School of Medicine, Ajou Univerisity, Suwon 442-749, Korea.

出版信息

Arch Pharm Res. 2004 Jan;27(1):68-76. doi: 10.1007/BF02980049.

Abstract

Mistletoe lectin has been reported to induce apoptosis in different cancer cell lines in vitro and to show antitumor activity against a variety of tumors in animal models. We previously demonstrated the Korean mistletoe lectin (Viscum album var. coloratum, VCA)-induced apoptosis by down-regulation of Bcl-2 and telomerase activity and by up-regulation of Bax through p53- and p21-independent pathway in hepatoma cells. In the present study, we observed the induction of apoptotic cell death through activation of caspase-3 and the inhibition of telomerase activity through transcriptional down-regulation of hTERT in the VCA-treated A253 cells. We also observed the inhibition of telomerase activity and induction of apoptosis resulted from dephosphorylation of Akt in the survival signaling pathways. In addition, combining VCA with the inhibitors of phosphatidylinositol 3-kinase (PI3-kinase) upstream of Akt, wortmannin and LY294002 showed an additive inhibitory effect of telomerase activity. In contrast, the inhibitor of protein phosphatase 2A (PP2A), okadaic acid inhibited VCA-induced dephosphorylation of Akt and inhibition of telomerase activity. Taken together, VCA induces apoptotic cell death through Akt signaling pathway in correlated with the inhibition of telomerase activity and the activation of caspase-3. From these results, together with our previous studies, we suggest that VCA triggers molecular changes that resulting in the inhibition of cell growth and the induction of apoptotic cell death of cancer cells, which suggest that VCA may be useful as chemotherapeutic agent for cancer cells.

摘要

据报道,槲寄生凝集素可在体外诱导不同癌细胞系凋亡,并在动物模型中显示出对多种肿瘤的抗肿瘤活性。我们之前证明了朝鲜槲寄生凝集素(Viscum album var. coloratum,VCA)通过下调Bcl-2和端粒酶活性以及通过p53和p21非依赖性途径上调Bax来诱导肝癌细胞凋亡。在本研究中,我们观察到在VCA处理的A253细胞中,通过激活caspase-3诱导凋亡细胞死亡,并通过hTERT的转录下调抑制端粒酶活性。我们还观察到存活信号通路中Akt的去磷酸化导致端粒酶活性的抑制和凋亡的诱导。此外,将VCA与Akt上游的磷脂酰肌醇3激酶(PI3激酶)抑制剂渥曼青霉素和LY294002联合使用,对端粒酶活性显示出相加抑制作用。相反,蛋白磷酸酶2A(PP2A)抑制剂冈田酸抑制VCA诱导的Akt去磷酸化和端粒酶活性抑制。综上所述,VCA通过Akt信号通路诱导凋亡细胞死亡,这与端粒酶活性的抑制和caspase-3的激活相关。根据这些结果以及我们之前的研究,我们认为VCA触发分子变化,导致癌细胞的细胞生长抑制和凋亡细胞死亡诱导,这表明VCA可能作为癌细胞的化疗药物有用。

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