• 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

腺相关病毒载体介导的 TMEM166 表达通过自噬和凋亡在体内外抑制人癌细胞生长。

Adenovirus vector-mediated expression of TMEM166 inhibits human cancer cell growth by autophagy and apoptosis in vitro and in vivo.

机构信息

Key Laboratory of Medical Immunology, Ministry of Health, Peking University Health Science Center, Beijing, China.

出版信息

Cancer Lett. 2013 Jan 1;328(1):126-34. doi: 10.1016/j.canlet.2012.08.032. Epub 2012 Sep 4.

DOI:10.1016/j.canlet.2012.08.032
PMID:22960574
Abstract

TMEM166 is a novel programmed cell death-related molecule. In this report, we constructed a recombinant adenovirus 5-TMEM166 vector (Ad5-TMEM166) and evaluated its expression and anti-tumor activities in vitro and in vivo. Cell viability analysis revealed that the adenovirus-mediated increase of TMEM166 inhibited tumor cell growth in a dose- and time-dependent manner. This inhibitory effect was mediated by both autophagy (via inhibition of mTOR and activation of p70S6K) and apoptosis (via caspase-3 activation), both of which contributed to cell death and suppression of tumorigenicity. Our data indicated that Ad5-TMEM166 may be a novel gene therapy candidate for cancer.

摘要

TMEM166 是一种新型的程序性细胞死亡相关分子。在本报告中,我们构建了重组腺病毒 5-TMEM166 载体(Ad5-TMEM166),并在体外和体内评估了其表达和抗肿瘤活性。细胞活力分析表明,腺病毒介导的 TMEM166 增加以剂量和时间依赖的方式抑制肿瘤细胞生长。这种抑制作用是通过自噬(通过抑制 mTOR 和激活 p70S6K)和细胞凋亡(通过 caspase-3 激活)介导的,这两者都导致细胞死亡和抑制肿瘤发生。我们的数据表明,Ad5-TMEM166 可能是癌症的一种新型基因治疗候选物。

相似文献

1
Adenovirus vector-mediated expression of TMEM166 inhibits human cancer cell growth by autophagy and apoptosis in vitro and in vivo.腺相关病毒载体介导的 TMEM166 表达通过自噬和凋亡在体内外抑制人癌细胞生长。
Cancer Lett. 2013 Jan 1;328(1):126-34. doi: 10.1016/j.canlet.2012.08.032. Epub 2012 Sep 4.
2
Adenovirus vector-mediated FAM176A overexpression induces cell death in human H1299 non-small cell lung cancer cells.腺病毒载体介导的FAM176A过表达诱导人H1299非小细胞肺癌细胞死亡。
BMB Rep. 2014 Feb;47(2):104-9. doi: 10.5483/bmbrep.2014.47.2.090.
3
The XAF1 tumor suppressor induces autophagic cell death via upregulation of Beclin-1 and inhibition of Akt pathway.XAF1 肿瘤抑制因子通过上调 Beclin-1 和抑制 Akt 通路诱导自噬细胞死亡。
Cancer Lett. 2011 Nov 28;310(2):170-80. doi: 10.1016/j.canlet.2011.06.037. Epub 2011 Jul 5.
4
A novel apoptotic mechanism of genetically engineered adenovirus-mediated tumour-specific p53 overexpression through E1A-dependent p21 and MDM2 suppression.通过 E1A 依赖性 p21 和 MDM2 抑制实现基因工程腺病毒介导的肿瘤特异性 p53 过表达的新型凋亡机制。
Eur J Cancer. 2012 Sep;48(14):2282-91. doi: 10.1016/j.ejca.2011.12.020. Epub 2012 Jan 13.
5
TMEM166, a novel transmembrane protein, regulates cell autophagy and apoptosis.跨膜蛋白166(TMEM166)是一种新型跨膜蛋白,可调节细胞自噬和凋亡。
Apoptosis. 2007 Aug;12(8):1489-502. doi: 10.1007/s10495-007-0073-9.
6
Enhanced growth inhibition of prostate cancer in vitro and in vivo by a recombinant adenovirus-mediated dual-aptamer modified drug delivery system.重组腺病毒介导的双适配体修饰药物递送系统增强前列腺癌的体外和体内生长抑制作用
Cancer Lett. 2016 Dec 28;383(2):230-242. doi: 10.1016/j.canlet.2016.10.003. Epub 2016 Oct 6.
7
Transmembrane Protein 166 and its Significance.跨膜蛋白 166 及其意义。
Protein Pept Lett. 2021;28(4):382-387. doi: 10.2174/0929866527666201002150316.
8
A novel capsid-modified oncolytic recombinant adenovirus type 5 for tumor-targeting gene therapy by intravenous route.一种新型衣壳修饰的溶瘤重组5型腺病毒,用于通过静脉途径进行肿瘤靶向基因治疗。
Oncotarget. 2016 Jul 26;7(30):47287-47301. doi: 10.18632/oncotarget.10075.
9
Cisplatin enhances the antitumor effect of tumor necrosis factor-related apoptosis-inducing ligand gene therapy via recruitment of the mitochondria-dependent death signaling pathway.顺铂通过募集线粒体依赖性死亡信号通路增强肿瘤坏死因子相关凋亡诱导配体基因治疗的抗肿瘤作用。
Cancer Gene Ther. 2008 Jun;15(6):356-70. doi: 10.1038/sj.cgt.7701120. Epub 2008 Feb 29.
10
[Effect and mechanism of an autophagy gene beclin 1 on cervical cancer HeLa cells].自噬基因Beclin 1对宫颈癌HeLa细胞的作用及机制
Zhonghua Fu Chan Ke Za Zhi. 2011 Feb;46(2):125-31.

引用本文的文献

1
Genetic Alchemy unveiled: MicroRNA-mediated gene therapy as the Artisan craft in the battlefront against hepatocellular carcinoma-a comprehensive chronicle of strategies and innovations.揭开基因炼金术的面纱:微小RNA介导的基因治疗在对抗肝细胞癌前线的精湛技艺——策略与创新的全面记录
Front Genet. 2024 Jun 10;15:1356972. doi: 10.3389/fgene.2024.1356972. eCollection 2024.
2
EVA1A reverses lenvatinib resistance in hepatocellular carcinoma through regulating PI3K/AKT/p53 signaling axis.EVA1A 通过调节 PI3K/AKT/p53 信号轴逆转肝癌对乐伐替尼的耐药性。
Apoptosis. 2024 Aug;29(7-8):1161-1184. doi: 10.1007/s10495-024-01967-0. Epub 2024 May 14.
3
Down-regulation of EVA1A by miR-103a-3p promotes hepatocellular carcinoma cells proliferation and migration.
miR-103a-3p 下调 EVA1A 促进肝癌细胞的增殖和迁移。
Cell Mol Biol Lett. 2022 Oct 22;27(1):93. doi: 10.1186/s11658-022-00388-8.
4
The Degradation of TMEM166 by Autophagy Promotes AMPK Activation to Protect SH-SY5Y Cells Exposed to MPP.自噬促进 TMEM166 降解以激活 AMPK 保护 MPP 诱导的 SH-SY5Y 细胞
Cells. 2022 Aug 30;11(17):2706. doi: 10.3390/cells11172706.
5
The Emerging Role of EVA1A in Different Types of Cancers.EVA1A 在不同类型癌症中的新兴作用。
Int J Mol Sci. 2022 Jun 15;23(12):6665. doi: 10.3390/ijms23126665.
6
Flubendazole induces mitochondrial dysfunction and DRP1-mediated mitophagy by targeting EVA1A in breast cancer.氟苯达唑通过靶向乳腺癌中的 EVA1A 诱导线粒体功能障碍和 DRP1 介导线粒体自噬。
Cell Death Dis. 2022 Apr 19;13(4):375. doi: 10.1038/s41419-022-04823-8.
7
Flubendazole Plays an Important Anti-Tumor Role in Different Types of Cancers.氟苯达唑在不同类型癌症中发挥重要的抗肿瘤作用。
Int J Mol Sci. 2022 Jan 4;23(1):519. doi: 10.3390/ijms23010519.
8
EVA1A Plays an Important Role by Regulating Autophagy in Physiological and Pathological Processes.EVA1A 在生理和病理过程中通过调控自噬发挥重要作用。
Int J Mol Sci. 2021 Jun 8;22(12):6181. doi: 10.3390/ijms22126181.
9
TMEM166 inhibits cell proliferation, migration and invasion in hepatocellular carcinoma via upregulating TP53.跨膜蛋白166通过上调TP53抑制肝癌细胞的增殖、迁移和侵袭。
Mol Cell Biochem. 2021 Feb;476(2):1151-1163. doi: 10.1007/s11010-020-03979-1. Epub 2020 Nov 16.
10
Liver-specific deletion of Eva1a/Tmem166 aggravates acute liver injury by impairing autophagy.Eva1a/Tmem166 在肝实质细胞中的缺失加剧急性肝损伤,导致自噬受损。
Cell Death Dis. 2018 Jul 10;9(7):768. doi: 10.1038/s41419-018-0800-x.