• 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

Ras的双面性:促凋亡还是抗凋亡?

Janus faces of ras: anti or pro-apoptotic?

作者信息

Arber N

机构信息

Department of Gastroenterology, GI Oncology Unit, Tel Aviv Sourasky Medical Center and Tel Aviv University, 64239 Tel Aviv, Israel.

出版信息

Apoptosis. 1999 Oct;4(5):383-8. doi: 10.1023/a:1009651406017.

DOI:10.1023/a:1009651406017
PMID:14634341
Abstract

Cell population homeostasis is a balance between cell proliferation on one hand and the rate of cell loss on the other hand. Normal tissue homeostasis requires the physiological deletion of cells by activation of apoptosis, a genetically determined program of autonomous cell death. ras is most probably the most important oncogene in human cancer. It is mutated in 30% of all tumors especially those of the gastrointestinal tract. In regulating apoptosis ras has many faces. it has both negative and positive effects depending on the stimulation and cell type. The responses of cells to ras signaling depends on the level of Ras expression, the activity of various pathways, and which of the cell cycle check points are functioning. New farnesyl transferase inhibitors and non-steroidal anti-inflammatory compounds may provide a new strategy for novel therapeutic modalities in the treatment of human cancer. The first clinical trials have been initiated, preliminary results are promising, although no firm results are yet available.

摘要

细胞群体稳态一方面是细胞增殖与另一方面细胞丢失速率之间的平衡。正常组织稳态需要通过激活凋亡(一种由基因决定的自主细胞死亡程序)来进行细胞的生理性清除。Ras很可能是人类癌症中最重要的癌基因。在所有肿瘤中,有30%发生了Ras突变,尤其是胃肠道肿瘤。在调节凋亡方面,Ras具有多种作用。根据刺激因素和细胞类型的不同,它既有负面影响也有正面影响。细胞对Ras信号的反应取决于Ras的表达水平、各种信号通路的活性以及哪些细胞周期检查点在发挥作用。新型法尼基转移酶抑制剂和非甾体类抗炎化合物可能为人类癌症治疗提供新的治疗策略。首批临床试验已经启动,初步结果很有前景,不过尚未有确凿的结果。

相似文献

1
Janus faces of ras: anti or pro-apoptotic?Ras的双面性:促凋亡还是抗凋亡?
Apoptosis. 1999 Oct;4(5):383-8. doi: 10.1023/a:1009651406017.
2
Growth inhibition of astrocytoma cells by farnesyl transferase inhibitors is mediated by a combination of anti-proliferative, pro-apoptotic and anti-angiogenic effects.法尼基转移酶抑制剂对星形细胞瘤细胞的生长抑制作用是由抗增殖、促凋亡和抗血管生成作用共同介导的。
Oncogene. 1999 Dec 9;18(52):7514-26. doi: 10.1038/sj.onc.1203105.
3
Oncogenic Ras triggers cell suicide through the activation of a caspase-independent cell death program in human cancer cells.致癌性Ras通过激活人癌细胞中一种不依赖半胱天冬酶的细胞死亡程序来触发细胞自杀。
Oncogene. 1999 Apr 1;18(13):2281-90. doi: 10.1038/sj.onc.1202538.
4
Farnesyl Transferase Inhibitors as Potential Anticancer Agents.法尼基转移酶抑制剂作为潜在的抗癌药物。
Mini Rev Med Chem. 2018;18(19):1611-1623. doi: 10.2174/1389557518666180801110342.
5
Farnesyl transferase inhibitors: a major breakthrough in anticancer therapy? Naples, 12 April 2002.法尼基转移酶抑制剂:抗癌治疗的重大突破?那不勒斯,2002年4月12日。
Anticancer Drugs. 2002 Sep;13(8):891-7. doi: 10.1097/00001813-200209000-00016.
6
Evaluation of farnesyl:protein transferase and geranylgeranyl:protein transferase inhibitor combinations in preclinical models.法尼基蛋白转移酶和香叶基香叶基蛋白转移酶抑制剂组合在临床前模型中的评估
Cancer Res. 2001 Dec 15;61(24):8758-68.
7
[Farnesyl transferase inhibitors--a novel agent for breast cancer].法尼基转移酶抑制剂——一种用于乳腺癌的新型药物
Ai Zheng. 2006 Apr;25(4):516-20.
8
HDAC inhibitors induce apoptosis but not cellular senescence in Gadd45α-deficient E1A+Ras cells.组蛋白去乙酰化酶抑制剂在缺乏Gadd45α的E1A+Ras细胞中诱导细胞凋亡,但不诱导细胞衰老。
Int J Biochem Cell Biol. 2014 Jun;51:102-10. doi: 10.1016/j.biocel.2014.03.031. Epub 2014 Apr 8.
9
Paradoxical activation of MEK/ERK signaling induced by B-Raf inhibition enhances DR5 expression and DR5 activation-induced apoptosis in Ras-mutant cancer cells.B-Raf抑制诱导的MEK/ERK信号通路的反常激活增强了Ras突变癌细胞中DR5的表达及DR5激活诱导的细胞凋亡。
Sci Rep. 2016 May 25;6:26803. doi: 10.1038/srep26803.
10
New drugs in cancer therapy, National Tumor Institute, Naples, 17-18 June 2004.癌症治疗中的新药,那不勒斯国家肿瘤研究所,2004年6月17 - 18日
Anticancer Drugs. 2005 Feb;16(2):211-21. doi: 10.1097/00001813-200502000-00014.

引用本文的文献

1
Targeting a newly established spontaneous feline fibrosarcoma cell line by gene transfer.通过基因转移靶向新建立的自发性猫纤维肉瘤细胞系。
PLoS One. 2012;7(5):e37743. doi: 10.1371/journal.pone.0037743. Epub 2012 May 30.
2
RAS oncogenes: weaving a tumorigenic web.RAS 癌基因:编织致癌网络。
Nat Rev Cancer. 2011 Oct 13;11(11):761-74. doi: 10.1038/nrc3106.
3
A common signaling cascade may underlie "addiction" to the Src, BCR-ABL, and EGF receptor oncogenes.一种常见的信号级联可能是对Src、BCR-ABL和表皮生长因子受体致癌基因“成瘾”的基础。
Cancer Cell. 2006 Nov;10(5):425-35. doi: 10.1016/j.ccr.2006.09.014.