• 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

在一种SV40转化的人尿道上皮细胞系中存在伴有平衡染色体改变的细胞遗传学不稳定性。

Cytogenetic instability with balanced chromosome changes in an SV40 transformed human uroepithelial cell line.

作者信息

Meisner L F, Wu S Q, Christian B J, Reznikoff C A

机构信息

State Laboratory of Hygiene, University of Wisconsin Health Sciences Center, Madison 53706.

出版信息

Cancer Res. 1988 Jun 1;48(11):3215-20.

PMID:2835156
Abstract

Cytogenetic analysis at the 15th, 34th, 50th, and 56th passages of an SV40 immortalized human uroepithelial cell line (SV-HUC-1) showed continuous chromosome change and marker formation. Throughout these passages the transformed cells maintained their epithelial morphology, were SV40 T antigen positive, did not shed infectious SV40 virus, and were repeatedly found to be nontumorigenic when innoculated into athymic nude mice. Each of the passages studied was characterized by extensive karyotypic changes due to formation, rearrangement, and disappearance of different markers. A marker involving chromosome 1 was stable at three of the passages studied, whereas markers involving the X chromosome changed at each passage studied. Because of the incorporation of several chromosomes or chromosome arms into markers, the karyotype was genetically balanced in the first passage studied, with no net loss or gain of chromosomal material despite a modal number of 44. In subsequent passages, despite continued instability and generation of new markers, there was a slight but additive loss of genomic balance which increased with time in culture. Since continued karyotypic rearrangements did not lead to tumorigenic conversion, it is probable that genetic instability coupled with selection for the most balanced genome may be important for the immortalization of this cell line.

摘要

对一株SV40永生化人尿道上皮细胞系(SV - HUC - 1)在第15、34、50和56代进行的细胞遗传学分析显示,染色体持续变化并形成标记物。在这些传代过程中,转化细胞保持其上皮形态,SV40 T抗原呈阳性,不释放具有感染性的SV40病毒,并且当接种到无胸腺裸鼠体内时,多次被发现无致瘤性。所研究的每一代都具有因不同标记物的形成、重排和消失而导致的广泛核型变化特征。一个涉及1号染色体的标记物在所研究的三代中保持稳定,而涉及X染色体的标记物在每一代所研究的过程中都发生变化。由于几条染色体或染色体臂并入标记物中,在所研究的第一代中核型在遗传上是平衡的,尽管众数为44,但染色体物质没有净损失或增加。在随后的传代中,尽管持续不稳定并产生新的标记物,但基因组平衡有轻微但累加的损失,且随着培养时间的延长而增加。由于持续的核型重排并未导致致瘤性转化,遗传不稳定与对最平衡基因组的选择相结合可能对该细胞系的永生化很重要。

相似文献

1
Cytogenetic instability with balanced chromosome changes in an SV40 transformed human uroepithelial cell line.在一种SV40转化的人尿道上皮细胞系中存在伴有平衡染色体改变的细胞遗传学不稳定性。
Cancer Res. 1988 Jun 1;48(11):3215-20.
2
Characterization of human uroepithelial cells immortalized in vitro by simian virus 40.由猿猴病毒40体外永生化的人尿道上皮细胞的特性分析
Cancer Res. 1987 Nov 15;47(22):6066-73.
3
Neoplastic progression by EJ/ras at different steps of transformation in vitro of human uroepithelial cells.EJ/ras在人尿道上皮细胞体外转化不同阶段的肿瘤进展。
Cancer Res. 1992 Feb 1;52(3):688-95.
4
EJ/ras neoplastic transformation of simian virus 40-immortalized human uroepithelial cells: a rare event.猿猴病毒40永生化人尿道上皮细胞的EJ/ras肿瘤转化:一个罕见事件。
Cancer Res. 1990 Aug 1;50(15):4779-86.
5
20q gain associates with immortalization: 20q13.2 amplification correlates with genome instability in human papillomavirus 16 E7 transformed human uroepithelial cells.20号染色体增益与永生化相关:20q13.2扩增与人乳头瘤病毒16 E7转化的人尿路上皮细胞中的基因组不稳定性相关。
Oncogene. 1997 Feb 6;14(5):551-60. doi: 10.1038/sj.onc.1200868.
6
Karyotype evolution of the human HBL-100 cell line and mapping of the integration site of SV40 DNA.人HBL - 100细胞系的核型进化及SV40 DNA整合位点的定位
Ann Genet. 1988;31(2):81-6.
7
In vitro radiation-induced neoplastic progression of low-grade uroepithelial tumors.低级别尿路上皮肿瘤的体外辐射诱导肿瘤进展
Radiat Res. 1994 Apr;138(1):86-92.
8
Non-tumorigenic SV40T immortalized human buccal epithelial cells show aneuploidy and genetic instability.
Anticancer Res. 1996 Sep-Oct;16(5A):2681-6.
9
Carcinogen-induced amplification of SV40 DNA inserted at 9q12-21.1 associated with chromosome breakage, deletions, and translocations in human uroepithelial cell transformation in vitro.致癌物诱导插入9q12 - 21.1的SV40 DNA扩增,这与体外人尿路上皮细胞转化过程中的染色体断裂、缺失和易位相关。
Genes Chromosomes Cancer. 1993 Nov;8(3):155-66. doi: 10.1002/gcc.2870080304.
10
Cancer-causing karyotypes: chromosomal equilibria between destabilizing aneuploidy and stabilizing selection for oncogenic function.致癌核型:不稳定非整倍体与致癌功能稳定选择之间的染色体平衡。
Cancer Genet Cytogenet. 2009 Jan 1;188(1):1-25. doi: 10.1016/j.cancergencyto.2008.08.016.

引用本文的文献

1
Cellular heterogeneity in the 16HBE14o airway epithelial line impacts biological readouts.16HBE14o 气道上皮细胞系中的细胞异质性会影响生物学检测结果。
Physiol Rep. 2023 Jun;11(11):e15700. doi: 10.14814/phy2.15700.
2
Conditional reprogramming: next generation cell culture.条件重编程:新一代细胞培养
Acta Pharm Sin B. 2020 Aug;10(8):1360-1381. doi: 10.1016/j.apsb.2020.01.011. Epub 2020 Jan 26.
3
Dual effects of radiation bystander signaling in urothelial cancer: purinergic-activation of apoptosis attenuates survival of urothelial cancer and normal urothelial cells.
辐射旁效应信号在尿路上皮癌中的双重作用:嘌呤能激活凋亡可减弱尿路上皮癌细胞和正常尿路上皮细胞的存活。
Oncotarget. 2017 Oct 24;8(57):97331-97343. doi: 10.18632/oncotarget.21995. eCollection 2017 Nov 14.
4
ADAM15 Is Functionally Associated with the Metastatic Progression of Human Bladder Cancer.ADAM15与人类膀胱癌的转移进展在功能上相关。
PLoS One. 2016 Mar 1;11(3):e0150138. doi: 10.1371/journal.pone.0150138. eCollection 2016.
5
Preclinical optimization of a broad-spectrum anti-bladder cancer tri-drug regimen via the Feedback System Control (FSC) platform.通过反馈系统控制(FSC)平台对一种广谱抗膀胱癌三联药物方案进行临床前优化。
Sci Rep. 2015 Jun 19;5:11464. doi: 10.1038/srep11464.
6
Regulation of the tumor suppressor FOXO3 by the thromboxane-A2 receptors in urothelial cancer.血栓素 A2 受体对尿路上皮癌中肿瘤抑制因子 FOXO3 的调控
PLoS One. 2014 Sep 9;9(9):e107530. doi: 10.1371/journal.pone.0107530. eCollection 2014.
7
MYC, TP53, and chromosome 17 copy-number alterations in multiple gastric cancer cell lines and in their parental primary tumors.多种胃癌细胞系及其亲本原发性肿瘤中的MYC、TP53和17号染色体拷贝数改变
J Biomed Biotechnol. 2011;2011:631268. doi: 10.1155/2011/631268. Epub 2011 Feb 23.
8
Transformation of SV40-immortalized human uroepithelial cells by 3-methylcholanthrene increases IFN- and Large T Antigen-induced transcripts.3-甲基胆蒽转化 SV40 永生化人尿路上皮细胞增加 IFN- 和大 T 抗原诱导的转录物。
Cancer Cell Int. 2010 Feb 23;10:4. doi: 10.1186/1475-2867-10-4.
9
PhenomiR: a knowledgebase for microRNA expression in diseases and biological processes.表型微小 RNA 数据库:疾病和生物过程中 microRNA 表达的知识库。
Genome Biol. 2010 Jan 20;11(1):R6. doi: 10.1186/gb-2010-11-1-r6.
10
Karyotypic changes associated with spontaneous acquisition and loss of tumorigenicity in a human transformed bronchial epithelial cell line: evidence for in vivo selection of transformed clones.人类转化支气管上皮细胞系中与肿瘤发生性的自发获得和丧失相关的核型变化:转化克隆体内选择的证据
In Vitro Cell Dev Biol Anim. 1998 Apr;34(4):283-9. doi: 10.1007/s11626-998-0004-2.