• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Behavior of the cell cycle-associated proteins in an unusual G0-arrestable cancer cell line.

作者信息

Ohta T, Fukuda M, Wanebo H J, Jogo K, Yamaguchi S

机构信息

First Department of Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.

出版信息

Exp Cell Res. 1996 May 25;225(1):85-92. doi: 10.1006/excr.1996.0159.

DOI:10.1006/excr.1996.0159
PMID:8635520
Abstract

An adenocarcinoma cell line which has the ability to arrest in G0 phase under exhausted culture conditions was established. Using the cell line, we investigated the expression of cell cycle-associated proteins including cdc2, cdk2, cyclin A, cyclin Dl, and Rb during entry into or withdrawal from the cell cycle. MAP kinase expression was also investigated as one of the most downstream proteins of the signal transduction of growth factors. The cells in the quiescent state did not express cdc2. In contrast, cdk2 was expressed weakly, and cyclin A and cyclin D1 were strongly expressed in the quiescent cells. The expression of cdk2 and cyclin D1 in the quiescent cells was reduced after stimulation by renewal of the medium and then increased, accompanied by Rb phosphorylation and cdc2 expression around the G1/S transition. Cdc2 and the hyperphosphorylated form of Rb disappeared as the cells became quiescent. MAP kinase expression was unchanged throughout all the phases analyzed. The results indicate that down-regulation of neither cdk2, cyclin A, cyclin D1, nor MAP kinase is necessary to arrest cells in G0, but that only Rb dephosphorylation and down-regulation of cdc2 are accompanied by an arrest of cell proliferation in G0 in the cell line.

摘要

相似文献

1
Behavior of the cell cycle-associated proteins in an unusual G0-arrestable cancer cell line.
Exp Cell Res. 1996 May 25;225(1):85-92. doi: 10.1006/excr.1996.0159.
2
Differential requirements for ras and the retinoblastoma tumor suppressor protein in the androgen dependence of prostatic adenocarcinoma cells.前列腺腺癌细胞雄激素依赖性中对Ras和视网膜母细胞瘤肿瘤抑制蛋白的不同需求。
Cell Growth Differ. 2000 Jul;11(7):361-72.
3
Expression and subcellular localization of CDK2 and cdc2 kinases and their common partner cyclin A in thyroid epithelial cells: comparison of cyclic AMP-dependent and -independent cell cycles.细胞周期蛋白依赖性激酶2(CDK2)和细胞周期蛋白依赖性激酶2(cdc2)及其共同伴侣细胞周期蛋白A在甲状腺上皮细胞中的表达与亚细胞定位:环磷酸腺苷(cAMP)依赖性和非依赖性细胞周期的比较
J Cell Physiol. 1996 Feb;166(2):256-73. doi: 10.1002/(SICI)1097-4652(199602)166:2<256::AID-JCP3>3.0.CO;2-O.
4
Restoration of retinoblastoma mediated signaling to Cdk2 results in cell cycle arrest.视网膜母细胞瘤介导的信号传导恢复至细胞周期蛋白依赖性激酶2会导致细胞周期停滞。
Oncogene. 2000 Apr 6;19(15):1857-67. doi: 10.1038/sj.onc.1203510.
5
Cyclin E-cdk2 activation is associated with cell cycle arrest and inhibition of DNA replication induced by the thymidylate synthase inhibitor Tomudex.细胞周期蛋白E-细胞周期蛋白依赖性激酶2的激活与胸苷酸合成酶抑制剂Tomudex诱导的细胞周期停滞和DNA复制抑制有关。
Exp Cell Res. 1999 Feb 25;247(1):189-99. doi: 10.1006/excr.1998.4346.
6
Inhibition of the melanoma cell cycle and regulation at the G1/S transition by 12-O-tetradecanoylphorbol-13-acetate (TPA) by modulation of CDK2 activity.通过调节CDK2活性,12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)对黑色素瘤细胞周期的抑制及在G1/S期转换的调控
Exp Cell Res. 1995 Nov;221(1):92-102. doi: 10.1006/excr.1995.1356.
7
Adhesion-dependent control of cyclin E/cdk2 activity and cell cycle progression in normal cells but not in Ha-ras transformed NRK cells.正常细胞中细胞周期蛋白E/细胞周期蛋白依赖性激酶2活性及细胞周期进程的黏附依赖性调控在Ha-ras转化的NRK细胞中不存在。
Exp Cell Res. 1996 Nov 25;229(1):86-92. doi: 10.1006/excr.1996.0346.
8
CaMK-II inhibition reduces cyclin D1 levels and enhances the association of p27kip1 with Cdk2 to cause G1 arrest in NIH 3T3 cells.钙/钙调蛋白依赖性蛋白激酶-II(CaMK-II)抑制作用可降低细胞周期蛋白D1水平,并增强p27kip1与细胞周期蛋白依赖性激酶2(Cdk2)的结合,从而导致NIH 3T3细胞出现G1期阻滞。
Exp Cell Res. 1998 May 1;240(2):218-27. doi: 10.1006/excr.1997.3925.
9
G1 phase accumulation induced by UCN-01 is associated with dephosphorylation of Rb and CDK2 proteins as well as induction of CDK inhibitor p21/Cip1/WAF1/Sdi1 in p53-mutated human epidermoid carcinoma A431 cells.UCN - 01诱导的G1期积累与p53突变的人表皮样癌A431细胞中Rb和CDK2蛋白的去磷酸化以及细胞周期蛋白依赖性激酶抑制剂p21/Cip1/WAF1/Sdi1的诱导有关。
Cancer Res. 1997 Apr 15;57(8):1495-501.
10
Down-regulation of the retinoblastoma protein (rb) is associated with rat oligodendrocyte differentiation.视网膜母细胞瘤蛋白(rb)的下调与大鼠少突胶质细胞分化有关。
Mol Cell Neurosci. 2002 Feb;19(2):250-62. doi: 10.1006/mcne.2001.1077.

引用本文的文献

1
High mobility group protein HMGA1 inhibits retinoblastoma protein-mediated cellular G0 arrest.高迁移率族蛋白HMGA1抑制视网膜母细胞瘤蛋白介导的细胞G0期停滞。
Cancer Sci. 2007 Dec;98(12):1893-901. doi: 10.1111/j.1349-7006.2007.00608.x. Epub 2007 Sep 17.