• 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

人类体细胞中的端粒酶表达不会诱导与转化表型相关的变化。

Telomerase expression in human somatic cells does not induce changes associated with a transformed phenotype.

作者信息

Jiang X R, Jimenez G, Chang E, Frolkis M, Kusler B, Sage M, Beeche M, Bodnar A G, Wahl G M, Tlsty T D, Chiu C P

机构信息

Geron Corporation, Menlo Park, California 94025, USA.

出版信息

Nat Genet. 1999 Jan;21(1):111-4. doi: 10.1038/5056.

DOI:10.1038/5056
PMID:9916802
Abstract

Expression of the human telomerase catalytic component, hTERT, in normal human somatic cells can reconstitute telomerase activity and extend their replicative lifespan. We report here that at twice the normal number of population doublings, telomerase-expressing human skin fibroblasts (BJ-hTERT) and retinal pigment epithelial cells (RPE-hTERT) retain normal growth control in response to serum deprivation, high cell density, G1 or G2 phase blockers and spindle inhibitors. In addition, we observed no cell growth in soft agar and detected no tumour formation in vivo. Thus, we find that telomerase expression in normal cells does not appear to induce changes associated with a malignant phenotype.

摘要

人类端粒酶催化亚基hTERT在正常人体体细胞中的表达可重建端粒酶活性并延长其复制寿命。我们在此报告,在群体倍增次数达到正常两倍时,表达端粒酶的人皮肤成纤维细胞(BJ-hTERT)和视网膜色素上皮细胞(RPE-hTERT)在血清剥夺、高细胞密度、G1或G2期阻滞剂以及纺锤体抑制剂作用下仍保持正常生长控制。此外,我们在软琼脂中未观察到细胞生长,在体内也未检测到肿瘤形成。因此,我们发现正常细胞中的端粒酶表达似乎不会诱导与恶性表型相关的变化。

相似文献

1
Telomerase expression in human somatic cells does not induce changes associated with a transformed phenotype.人类体细胞中的端粒酶表达不会诱导与转化表型相关的变化。
Nat Genet. 1999 Jan;21(1):111-4. doi: 10.1038/5056.
2
Immortalization of bovine capillary endothelial cells by hTERT alone involves inactivation of endogenous p16INK4A/pRb.仅通过hTERT使牛毛细血管内皮细胞永生化涉及内源性p16INK4A/pRb的失活。
FASEB J. 2003 Apr;17(6):764-6. doi: 10.1096/fj.02-0599fje. Epub 2003 Feb 5.
3
Absence of cancer-associated changes in human fibroblasts immortalized with telomerase.用端粒酶永生化的人成纤维细胞中不存在癌症相关变化。
Nat Genet. 1999 Jan;21(1):115-8. doi: 10.1038/5063.
4
Both Rb/p16INK4a inactivation and telomerase activity are required to immortalize human epithelial cells.Rb/p16INK4a失活和端粒酶活性都是使人类上皮细胞永生化所必需的。
Nature. 1998 Nov 5;396(6706):84-8. doi: 10.1038/23962.
5
Prolonged culture of telomerase-immortalized human fibroblasts leads to a premalignant phenotype.端粒酶永生化的人成纤维细胞长期培养会导致癌前表型。
Cancer Res. 2003 Nov 1;63(21):7147-57.
6
Genetic and epigenetic changes in human epithelial cells immortalized by telomerase.端粒酶永生化的人上皮细胞中的遗传和表观遗传变化。
Am J Pathol. 2000 May;156(5):1537-47. doi: 10.1016/S0002-9440(10)65025-0.
7
A novel human cancer culture model for the study of prostate cancer.一种用于前列腺癌研究的新型人类癌症培养模型。
Oncogene. 2001 Nov 29;20(55):8036-41. doi: 10.1038/sj.onc.1205002.
8
Mass cultured human fibroblasts overexpressing hTERT encounter a growth crisis following an extended period of proliferation.大量培养的过表达hTERT的人成纤维细胞在长时间增殖后会遭遇生长危机。
Exp Cell Res. 2000 Sep 15;259(2):336-50. doi: 10.1006/excr.2000.4982.
9
Human telomerase reverse transcriptase promoter regulation in normal and malignant human ovarian epithelial cells.正常与恶性人卵巢上皮细胞中人类端粒酶逆转录酶启动子调控
Cancer Res. 2001 Jul 15;61(14):5529-36.
10
Telomerase activity is sufficient to bypass replicative senescence in human limbal and conjunctival but not corneal keratinocytes.端粒酶活性足以使人类角膜缘和结膜角质形成细胞绕过复制性衰老,但对角膜角质形成细胞无效。
Eur J Cell Biol. 2004 Dec;83(11-12):691-700. doi: 10.1078/0171-9335-00424.

引用本文的文献

1
The reference genome of the human diploid cell line RPE-1.人类二倍体细胞系RPE-1的参考基因组。
Nat Commun. 2025 Sep 12;16(1):7751. doi: 10.1038/s41467-025-62428-z.
2
Supra-second tracking and live-cell karyotyping reveal principles of mitotic chromosome dynamics.超秒级追踪和活细胞染色体组型分析揭示有丝分裂染色体动力学原理。
Nat Cell Biol. 2025 Apr;27(4):654-667. doi: 10.1038/s41556-025-01637-6. Epub 2025 Apr 4.
3
CRISPR targeting of SNPs associated with age-related macular degeneration in ARPE-19 cells: a potential model for manipulating the complement system.
在ARPE-19细胞中对与年龄相关性黄斑变性相关的单核苷酸多态性进行CRISPR靶向:一种操纵补体系统的潜在模型。
Gene Ther. 2025 Mar;32(2):132-141. doi: 10.1038/s41434-025-00522-z. Epub 2025 Mar 18.
4
Robust p53 phenotypes and prospective downstream targets in telomerase-immortalized human cells.端粒酶永生化人类细胞中强大的p53表型及潜在下游靶点
Oncotarget. 2025 Feb 18;16:79-100. doi: 10.18632/oncotarget.28690.
5
Co-isolation of human donor eye cells and development of oncogene-mutated melanocytes to study uveal melanoma.共分离人供体眼细胞并培养致癌基因突变的黑色素细胞以研究葡萄膜黑色素瘤。
BMC Biol. 2025 Jan 21;23(1):16. doi: 10.1186/s12915-025-02118-w.
6
Review of hTERT-Immortalized Cells: How to Assess Immortality and Confirm Identity.人端粒酶逆转录酶永生化细胞综述:如何评估永生化及确认身份。
Int J Mol Sci. 2024 Dec 4;25(23):13054. doi: 10.3390/ijms252313054.
7
Evaluation of mesenchymal stem cells as an model for inherited retinal diseases.间充质干细胞作为遗传性视网膜疾病模型的评估。
Front Cell Dev Biol. 2024 Nov 15;12:1455140. doi: 10.3389/fcell.2024.1455140. eCollection 2024.
8
Extended replicative lifespan of primary resting T cells by CRISPR/dCas9-based epigenetic modifiers and transcriptional activators.基于 CRISPR/dCas9 的表观遗传修饰物和转录激活物延长原初静息 T 细胞的复制寿命。
Cell Mol Life Sci. 2024 Sep 17;81(1):407. doi: 10.1007/s00018-024-05415-9.
9
Replication fork stalling in late S-phase elicits nascent strand degradation by DNA mismatch repair.复制叉在晚期 S 期停滞会通过 DNA 错配修复引发新生链降解。
Nucleic Acids Res. 2024 Oct 14;52(18):10999-11013. doi: 10.1093/nar/gkae721.
10
Small GTPase ActIvitY ANalyzing (SAIYAN) system: A method to detect GTPase activation in living cells.小 GTPase 活性分析(SAIYAN)系统:一种检测活细胞中 GTPase 激活的方法。
J Cell Biol. 2024 Oct 7;223(10). doi: 10.1083/jcb.202403179. Epub 2024 Aug 5.