• 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

膀胱移行细胞癌中Ha-ras和Ki-ras癌基因的低频突变

Low-frequency mutation of Ha-ras and Ki-ras oncogenes in transitional cell carcinoma of the bladder.

作者信息

Olderøy G, Daehlin L, Ogreid D

机构信息

Center for Molecular Medicine, Haukeland Hospital, Bergen, Norway.

出版信息

Anticancer Res. 1998 Jul-Aug;18(4A):2675-8.

PMID:9703927
Abstract

UNLABELLED

BACKGROUND, PATIENTS AND METHODS: The objective was to study the frequency of mutations of Ha-ras and Ki-ras oncogenes in bladder tumours. Transitional cell tumours of the bladder from 55 patients were subjected to analyses of Ha-ras and Ki-ras oncogenes using a variety of techniques including sequencing to detect mutations.

RESULTS

Two tumours (4%) exhibited mutation of the Ki-ras oncogene, both tumours were fast growing and invasive. We did not detect Ha-ras mutation in any of the samples. Nineteen tumours (35%) with established invasion of the detrusor muscle, did not reveal any mutation.

CONCLUSION

Analyses of ras oncogenes seem to be of limited value for the biological assessment of transitional cell carcinomas.

摘要

未标注

背景、患者与方法:目的是研究膀胱肿瘤中Ha-ras和Ki-ras癌基因的突变频率。对55例患者的膀胱移行细胞肿瘤采用包括测序在内的多种技术进行Ha-ras和Ki-ras癌基因分析以检测突变。

结果

2例肿瘤(4%)表现出Ki-ras癌基因突变,这2例肿瘤均生长迅速且具有侵袭性。我们在任何样本中均未检测到Ha-ras突变。19例(35%)已证实有逼尿肌浸润的肿瘤未显示任何突变。

结论

ras癌基因分析对移行细胞癌的生物学评估似乎价值有限。

相似文献

1
Low-frequency mutation of Ha-ras and Ki-ras oncogenes in transitional cell carcinoma of the bladder.膀胱移行细胞癌中Ha-ras和Ki-ras癌基因的低频突变
Anticancer Res. 1998 Jul-Aug;18(4A):2675-8.
2
Activation of RAS family genes in urothelial carcinoma.尿路上皮癌中RAS家族基因的激活
J Urol. 2009 May;181(5):2312-9. doi: 10.1016/j.juro.2009.01.011. Epub 2009 Mar 19.
3
Mutations of RAS gene family in specimens of bladder cancer.膀胱癌标本中RAS基因家族的突变
Urol J. 2008 Fall;5(4):237-42.
4
H-ras mutations in rat urinary bladder carcinomas induced by N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide and sodium saccharin, sodium ascorbate, or related salts.由N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺与糖精钠、抗坏血酸钠或相关盐类诱导的大鼠膀胱癌中的H-ras突变
Cancer Res. 1991 Jul 1;51(13):3471-5.
5
Transgenic rats carrying copies of the human c-Ha-ras proto-oncogene exhibit enhanced susceptibility to N-butyl-N-(4-hydroxybutyl)nitrosamine bladder carcinogenesis.携带人类c-Ha-ras原癌基因拷贝的转基因大鼠对N-丁基-N-(4-羟丁基)亚硝胺膀胱致癌作用的易感性增强。
Carcinogenesis. 2000 Jul;21(7):1391-6.
6
Genetic aberrations of the K-ras proto-oncogene in bladder cancer in Kashmiri population.克什米尔人群膀胱癌中K-ras原癌基因的遗传畸变
Urol J. 2010 Summer;7(3):168-73.
7
Ha-ras induction of the invasive phenotype results in up-regulation of epidermal growth factor receptors and altered responsiveness to epidermal growth factor in human papillary transitional cell carcinoma cells.Ha-ras诱导侵袭性表型导致人乳头状移行细胞癌细胞中表皮生长因子受体上调以及对表皮生长因子的反应性改变。
Cancer Res. 1991 Aug 15;51(16):4486-91.
8
Detection of a rare point mutation in Ki-ras of a human bladder cancer xenograft by polymerase chain reaction and direct sequencing.通过聚合酶链反应和直接测序检测人膀胱癌异种移植瘤中Ki-ras基因的罕见点突变。
Urol Res. 1992;20(2):121-6. doi: 10.1007/BF00296523.
9
Sequencing analysis of Ha-, Ki-, and N-ras genes in rat urinary bladder tumors induced by N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide (FANFT) and sodium saccharin.
Teratog Carcinog Mutagen. 1993;13(5):225-33. doi: 10.1002/tcm.1770130504.
10
p53 Gene mutations in superficial bladder cancer.浅表性膀胱癌中的p53基因突变
Urol Int. 2004;73(3):212-8. doi: 10.1159/000080830.

引用本文的文献

1
Mutational analysis of hotspots in patients with urothelial carcinoma of the bladder.膀胱尿路上皮癌患者热点区域的突变分析。
World J Clin Oncol. 2020 Aug 24;11(8):614-628. doi: 10.5306/wjco.v11.i8.614.
2
Ras Isoprenylation and pAkt Inhibition by Zoledronic Acid and Fluvastatin Enhances Paclitaxel Activity in T24 Bladder Cancer Cells.唑来膦酸和氟伐他汀通过抑制 Ras 异戊烯化和 pAkt 增强 T24 膀胱癌细胞中紫杉醇的活性。
Cancers (Basel). 2011 Feb 14;3(1):662-74. doi: 10.3390/cancers3010662.
3
Simultaneous activation of Kras and inactivation of p53 induces soft tissue sarcoma and bladder urothelial hyperplasia.
同时激活 Kras 和失活 p53 可诱导软组织肉瘤和膀胱尿路上皮增生。
PLoS One. 2013 Sep 18;8(9):e74809. doi: 10.1371/journal.pone.0074809. eCollection 2013.
4
The prevalence and prognostic significance of KRAS mutation in bladder cancer, chronic myeloid leukemia and colorectal cancer.KRAS 突变在膀胱癌、慢性髓性白血病和结直肠癌中的流行情况及其预后意义。
Mol Biol Rep. 2013 Jun;40(6):4109-14. doi: 10.1007/s11033-013-2512-8. Epub 2013 May 3.
5
A systematic study of gene mutations in urothelial carcinoma; inactivating mutations in TSC2 and PIK3R1.对尿路上皮癌中的基因突变进行系统研究;TSC2 和 PIK3R1 的失活突变。
PLoS One. 2011 Apr 14;6(4):e18583. doi: 10.1371/journal.pone.0018583.
6
K-Ras and β-catenin mutations cooperate with Fgfr3 mutations in mice to promote tumorigenesis in the skin and lung, but not in the bladder.K-Ras 和 β-catenin 突变与 Fgfr3 突变协同作用促进小鼠皮肤和肺部肿瘤的发生,但不促进膀胱肿瘤的发生。
Dis Model Mech. 2011 Jul;4(4):548-55. doi: 10.1242/dmm.006874. Epub 2011 Apr 18.
7
Ras mutation cooperates with β-catenin activation to drive bladder tumourigenesis.Ras 突变与β-catenin 激活协同作用驱动膀胱癌发生。
Cell Death Dis. 2011 Mar 3;2(3):e124. doi: 10.1038/cddis.2011.7.
8
Inhibitory effect of flavonoids on mutant H-Rasp protein.类黄酮对突变型H-Rasp蛋白的抑制作用。
Bioinformation. 2010 Jun 15;5(1):11-5. doi: 10.6026/97320630005011.
9
Depression and cancer risk: 24 years of follow-up of the Baltimore Epidemiologic Catchment Area sample.抑郁与癌症风险:巴尔的摩流行病学抽样调查区样本 24 年随访研究。
Cancer Causes Control. 2010 Feb;21(2):191-9. doi: 10.1007/s10552-009-9449-1. Epub 2009 Nov 3.
10
Behavioral genetics of the depression/cancer correlation: a look at the Ras oncogene family and the 'cerebral diabetes paradigm'.抑郁/癌症相关性的行为遗传学:审视Ras癌基因家族与“大脑糖尿病范式”。
J Mol Neurosci. 2008 Jul;35(3):307-22. doi: 10.1007/s12031-008-9078-2. Epub 2008 Jun 18.