• 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

PTEN/MMAC1肿瘤抑制因子诱导的细胞死亡可被AKT/蛋白激酶B致癌基因挽救。

The PTEN/MMAC1 tumor suppressor induces cell death that is rescued by the AKT/protein kinase B oncogene.

作者信息

Li J, Simpson L, Takahashi M, Miliaresis C, Myers M P, Tonks N, Parsons R

机构信息

Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.

出版信息

Cancer Res. 1998 Dec 15;58(24):5667-72.

PMID:9865719
Abstract

PTEN/MMAC1 is a tumor suppressor gene that is mutated in a variety of cancers. PTEN encodes a phosphatase that recognizes phosphoprotein substrates and the phospholipid, phosphatidylinositol-3,4,5-triphosphate. PTEN inhibited cell growth and/or colony formation in all of the epithelial lines tested with one exception. The decrease in cellular proliferation was associated with an induction of apoptosis and an inhibition of signaling through the phosphatidylinositol 3'-kinase pathway. Akt/protein kinase B, a gene whose antiapoptotic function is regulated by phosphatidylinositol-3,4,5-triphosphate, was able to rescue cells from PTEN-dependent death. PTEN, therefore, appears to suppress tumor growth by regulating phosphatidylinositol 3'-kinase signaling.

摘要

PTEN/MMAC1是一种肿瘤抑制基因,在多种癌症中发生突变。PTEN编码一种磷酸酶,该磷酸酶可识别磷蛋白底物和磷脂酰肌醇-3,4,5-三磷酸。除一个例外情况外,PTEN在所有测试的上皮细胞系中均抑制细胞生长和/或集落形成。细胞增殖的减少与细胞凋亡的诱导以及通过磷脂酰肌醇3'-激酶途径的信号传导抑制有关。Akt/蛋白激酶B是一种抗凋亡功能受磷脂酰肌醇-3,4,5-三磷酸调节的基因,它能够使细胞从依赖PTEN的死亡中获救。因此,PTEN似乎通过调节磷脂酰肌醇3'-激酶信号传导来抑制肿瘤生长。

相似文献

1
The PTEN/MMAC1 tumor suppressor induces cell death that is rescued by the AKT/protein kinase B oncogene.PTEN/MMAC1肿瘤抑制因子诱导的细胞死亡可被AKT/蛋白激酶B致癌基因挽救。
Cancer Res. 1998 Dec 15;58(24):5667-72.
2
PTEN suppresses breast cancer cell growth by phosphatase activity-dependent G1 arrest followed by cell death.PTEN通过磷酸酶活性依赖性的G1期阻滞继而引发细胞死亡来抑制乳腺癌细胞的生长。
Cancer Res. 1999 Nov 15;59(22):5808-14.
3
The PTEN/MMAC1/TEP tumor suppressor gene decreases cell growth and induces apoptosis and anoikis in breast cancer cells.PTEN/MMAC1/TEP肿瘤抑制基因可降低乳腺癌细胞的生长速度,并诱导其凋亡和失巢凋亡。
Oncogene. 1999 Nov 25;18(50):7034-45. doi: 10.1038/sj.onc.1203183.
4
PTEN tumour suppressor is linked to the cell cycle control through the retinoblastoma protein.PTEN肿瘤抑制因子通过视网膜母细胞瘤蛋白与细胞周期调控相关联。
Oncogene. 1999 Dec 9;18(52):7462-8. doi: 10.1038/sj.onc.1203151.
5
PTEN/MMAC1/TEP1 suppresses the tumorigenicity and induces G1 cell cycle arrest in human glioblastoma cells.PTEN/MMAC1/TEP1抑制人胶质母细胞瘤细胞的致瘤性并诱导G1期细胞周期阻滞。
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15406-11. doi: 10.1073/pnas.95.26.15406.
6
The PTEN/MMAC1 tumor suppressor phosphatase functions as a negative regulator of the phosphoinositide 3-kinase/Akt pathway.PTEN/MMAC1肿瘤抑制磷酸酶作为磷酸肌醇3激酶/Akt信号通路的负调节因子发挥作用。
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15587-91. doi: 10.1073/pnas.95.26.15587.
7
Regulation of G1 progression by the PTEN tumor suppressor protein is linked to inhibition of the phosphatidylinositol 3-kinase/Akt pathway.PTEN肿瘤抑制蛋白对G1期进程的调控与磷脂酰肌醇3激酶/Akt信号通路的抑制相关。
Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2110-5. doi: 10.1073/pnas.96.5.2110.
8
Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors.在表达表皮生长因子受体(EGF receptor)的肿瘤细胞中,第10号染色体缺失的磷酸酶及张力蛋白同源物(PTEN)/MMAC1/TEP的缺失会抵消表皮生长因子受体酪氨酸激酶抑制剂的抗肿瘤作用。
Oncogene. 2003 May 8;22(18):2812-22. doi: 10.1038/sj.onc.1206388.
9
MMAC1/PTEN inhibits cell growth and induces chemosensitivity to doxorubicin in human bladder cancer cells.MMAC1/PTEN抑制人膀胱癌细胞的生长并诱导其对阿霉素的化学敏感性。
Oncogene. 2000 Nov 9;19(47):5406-12. doi: 10.1038/sj.onc.1203918.
10
PTEN: life as a tumor suppressor.PTEN:作为肿瘤抑制因子的历程
Exp Cell Res. 2001 Mar 10;264(1):29-41. doi: 10.1006/excr.2000.5130.

引用本文的文献

1
Protopanaxatriol, a ginsenoside metabolite, induces apoptosis in colorectal cancer cells and arrests their cell cycle by targeting AKT.原人参三醇,一种人参皂苷代谢产物,通过靶向AKT诱导结肠癌细胞凋亡并使其细胞周期停滞。
J Ginseng Res. 2025 Sep;49(5):488-501. doi: 10.1016/j.jgr.2025.03.012. Epub 2025 Apr 3.
2
Epidermal growth factor receptor in placental health and disease: pathways, dysfunction, and chemical disruption.表皮生长因子受体在胎盘健康与疾病中的作用:信号通路、功能障碍及化学干扰
Toxicol Sci. 2025 May 1;205(1):11-27. doi: 10.1093/toxsci/kfaf024.
3
Deubiquitinase processing of a non-natural linkage of ubiquitinated-PTEN.
去泛素化酶对泛素化PTEN非天然连接的加工处理
Bioorg Chem. 2025 Apr;157:108223. doi: 10.1016/j.bioorg.2025.108223. Epub 2025 Jan 30.
4
Rhabdomyosarcoma: Current Therapy, Challenges, and Future Approaches to Treatment Strategies.横纹肌肉瘤:当前的治疗方法、挑战及未来的治疗策略途径
Cancers (Basel). 2023 Nov 2;15(21):5269. doi: 10.3390/cancers15215269.
5
Role of miRNA in Melanoma Development and Progression.miRNA 在黑色素瘤发生和进展中的作用。
Int J Mol Sci. 2022 Dec 22;24(1):201. doi: 10.3390/ijms24010201.
6
LAPTM5 mediates immature B cell apoptosis and B cell tolerance by regulating the WWP2-PTEN-AKT pathway.LAPTM5 通过调控 WWP2-PTEN-AKT 通路介导未成熟 B 细胞凋亡和 B 细胞耐受。
Proc Natl Acad Sci U S A. 2022 Sep 6;119(36):e2205629119. doi: 10.1073/pnas.2205629119. Epub 2022 Aug 29.
7
Comprehensive characterization of PTEN mutational profile in a series of 34,129 colorectal cancers.对 34129 例结直肠癌中 PTEN 突变谱进行全面特征分析。
Nat Commun. 2022 Mar 25;13(1):1618. doi: 10.1038/s41467-022-29227-2.
8
Resistance mechanisms to inhibitors of p53-MDM2 interactions in cancer therapy: can we overcome them?癌症治疗中针对p53-MDM2相互作用抑制剂的耐药机制:我们能否克服它们?
Cell Mol Biol Lett. 2021 Dec 15;26(1):53. doi: 10.1186/s11658-021-00293-6.
9
PTEN inhibition leads to the development of resistance to novel isoquinoline derivative TNBG-5602 in human liver cancer cells.PTEN抑制导致人肝癌细胞对新型异喹啉衍生物TNBG - 5602产生耐药性。
Am J Cancer Res. 2021 Sep 15;11(9):4515-4527. eCollection 2021.
10
The PI3K/Akt signaling axis in Alzheimer's disease: a valuable target to stimulate or suppress?阿尔茨海默病中 PI3K/Akt 信号通路:刺激还是抑制?一个有价值的靶点
Cell Stress Chaperones. 2021 Nov;26(6):871-887. doi: 10.1007/s12192-021-01231-3. Epub 2021 Aug 13.