• 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

建立并鉴定人膀胱癌细胞系 BexBra1、BexBra2 和 BexBra4。

Establishment and characterization of human bladder cancer cell lines BexBra1, BexBra2, and BexBra4.

机构信息

Laboratory of Medical Investigation, Urology Department–LIM55, University of Sao Paulo Medical School, São Paulo, São Paulo, Brazil.

出版信息

In Vitro Cell Dev Biol Anim. 2010 Feb;46(2):131-9. doi: 10.1007/s11626-009-9252-z.

DOI:10.1007/s11626-009-9252-z
PMID:19915932
Abstract

Bladder cancer (BC) is the fourth most common cancer in the USA. In Brazil, BC represents 3% of the total existing carcinomas in the population and represents the second highest incidence among urological tumors. The majority of bladder cancer cell lines available were derived from Caucasians and established in the seventies or eighties. Thus, neoplasia development in these cells likely occurred in environment conditions vastly different than today. In the present study, we report the establishment and characterization of three Brazilian bladder cancer cell lines (BexBra1, BexBra2, and BexBra4). These cell lines may be helpful for dissecting the genetic and epigenetic aspects that trigger the progression of BC. Moreover, the development of a Brazilian representative of the disease will allow us to investigate the potential inter-racial differences of malignancy-associated phenotypes in bladder cancer.

摘要

膀胱癌(BC)是美国第四大常见癌症。在巴西,BC 占人群中现有癌总数的 3%,是泌尿系统肿瘤中发病率第二高的肿瘤。目前可用的大多数膀胱癌细胞系均源自白种人,并且是在 70 年代或 80 年代建立的。因此,这些细胞中的肿瘤发生很可能发生在与今天大不相同的环境条件下。在本研究中,我们报告了三种巴西膀胱癌细胞系(BexBra1、BexBra2 和 BexBra4)的建立和特征。这些细胞系可能有助于剖析引发 BC 进展的遗传和表观遗传方面。此外,开发出具有代表性的巴西疾病模型将使我们能够研究膀胱癌中与恶性表型相关的潜在种族间差异。

相似文献

1
Establishment and characterization of human bladder cancer cell lines BexBra1, BexBra2, and BexBra4.建立并鉴定人膀胱癌细胞系 BexBra1、BexBra2 和 BexBra4。
In Vitro Cell Dev Biol Anim. 2010 Feb;46(2):131-9. doi: 10.1007/s11626-009-9252-z.
2
Cytogenetic characterization of the murine bladder cancer model MB49 and the derived invasive line MB49-I.小鼠膀胱癌模型MB49及其衍生的侵袭性细胞系MB49-I的细胞遗传学特征。
Cancer Genet. 2012 Apr;205(4):168-76. doi: 10.1016/j.cancergen.2012.02.002.
3
Establishment of a novel experimental model for muscle-invasive bladder cancer using a dog bladder cancer organoid culture.建立一种新型的肌层浸润性膀胱癌实验模型,使用犬膀胱癌类器官培养。
Cancer Sci. 2019 Sep;110(9):2806-2821. doi: 10.1111/cas.14118. Epub 2019 Jul 23.
4
Establishment and characterization of androgen-independent human prostate cancer cell lines, PcBra1, PcBra2, and PcBra3.建立并鉴定雄激素非依赖性人前列腺癌细胞系 PcBra1、PcBra2 和 PcBra3。
In Vitro Cell Dev Biol Anim. 2010 Feb;46(2):123-30. doi: 10.1007/s11626-009-9249-7. Epub 2009 Dec 8.
5
[THE MAIN STAGES OF THE PREPARATION OF VIABLE TUMOR CELLS OF BLADDER CANCER: FROM ISOLATION OF THE TUMOR MATERIAL TILL CRYOPRESERVATION OF CELL LINES].
Georgian Med News. 2017 May(266):19-26.
6
[CRITERIA FOR SELECTION OF TUMOR CELLS AND PROSPECTS FOR SPECIFIC IMMUNOTHERAPY FOR BLADDER CANCER].
Georgian Med News. 2017 May(266):26-34.
7
Establishment and characterization of a new squamous cell carcinoma cell line, TMUU-08, derived from human bladder cancer.
Hum Cell. 2009 Feb;22(1):25-9. doi: 10.1111/j.1749-0774.2008.00064.x.
8
[Bladder carcinoma cell lines as models of the pathobiology of bladder cancer. Review of the literature and establishment of a new progression series].[膀胱癌细胞系作为膀胱癌病理生物学模型。文献综述及新进展系列的建立]
Urologe A. 2008 Jun;47(6):724-34. doi: 10.1007/s00120-008-1687-4.
9
Disruption of the FA/BRCA pathway in bladder cancer.膀胱癌中FA/BRCA通路的破坏。
Cytogenet Genome Res. 2007;118(2-4):166-76. doi: 10.1159/000108297.
10
Decreased Fas expression in advanced-stage bladder cancer is not related to p53 status.晚期膀胱癌中Fas表达降低与p53状态无关。
Urology. 2004 Feb;63(2):392-7. doi: 10.1016/j.urology.2003.08.023.

引用本文的文献

1
Classification of bladder cancer cell lines according to regulon activity.根据调控子活性对膀胱癌细胞系进行分类。
Turk J Biol. 2021 Dec 14;45(6):656-666. doi: 10.3906/biy-2107-72. eCollection 2021.
2
Characterization of three newly established rat sarcoma cell clones.三种新建立的大鼠肉瘤细胞克隆的特征。
In Vitro Cell Dev Biol Anim. 2012 Dec;48(10):610-8. doi: 10.1007/s11626-012-9563-3. Epub 2012 Nov 13.

本文引用的文献

1
Cancer statistics, 2009.2009年癌症统计数据。
CA Cancer J Clin. 2009 Jul-Aug;59(4):225-49. doi: 10.3322/caac.20006. Epub 2009 May 27.
2
[Bladder carcinoma cell lines as models of the pathobiology of bladder cancer. Review of the literature and establishment of a new progression series].[膀胱癌细胞系作为膀胱癌病理生物学模型。文献综述及新进展系列的建立]
Urologe A. 2008 Jun;47(6):724-34. doi: 10.1007/s00120-008-1687-4.
3
Molecular pathways in invasive bladder cancer: new insights into mechanisms, progression, and target identification.
浸润性膀胱癌的分子通路:对机制、进展及靶点识别的新见解
J Clin Oncol. 2006 Dec 10;24(35):5552-64. doi: 10.1200/JCO.2006.08.2073.
4
Status of the p53, p16, RB1, and HER-2 genes and chromosomes 3, 7, 9, and 17 in advanced bladder cancer: correlation with adjacent mucosa and pathological parameters.晚期膀胱癌中p53、p16、RB1和HER-2基因以及3、7、9和17号染色体的状态:与相邻黏膜及病理参数的相关性
J Clin Pathol. 2005 Apr;58(4):367-71. doi: 10.1136/jcp.2004.021154.
5
FGFR3 and TP53 gene mutations define two distinct pathways in urothelial cell carcinoma of the bladder.成纤维细胞生长因子受体3(FGFR3)和肿瘤蛋白p53(TP53)基因突变在膀胱尿路上皮癌中定义了两条不同的途径。
Cancer Res. 2003 Dec 1;63(23):8108-12.
6
Therapeutic approaches to bladder cancer: identifying targets and mechanisms.
Crit Rev Oncol Hematol. 2003 Jun 27;46 Suppl:S67-83. doi: 10.1016/s1040-8428(03)00066-0.
7
Classification and grading of the non-invasive urothelial neoplasms: recent advances and controversies.非侵袭性尿路上皮肿瘤的分类与分级:最新进展与争议
J Clin Pathol. 2003 Feb;56(2):91-5. doi: 10.1136/jcp.56.2.91.
8
Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound.一种低分子量化合物使突变型p53的肿瘤抑制功能得以恢复。
Nat Med. 2002 Mar;8(3):282-8. doi: 10.1038/nm0302-282.
9
Curcumin inhibits activation of Vgamma9Vdelta2 T cells by phosphoantigens and induces apoptosis involving apoptosis-inducing factor and large scale DNA fragmentation.姜黄素可抑制磷酸抗原对Vγ9Vδ2 T细胞的激活,并诱导细胞凋亡,此过程涉及凋亡诱导因子及大规模DNA片段化。
J Immunol. 2001 Sep 15;167(6):3454-62. doi: 10.4049/jimmunol.167.6.3454.
10
Short tandem repeat profiling provides an international reference standard for human cell lines.短串联重复序列分析为人类细胞系提供了国际参考标准。
Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):8012-7. doi: 10.1073/pnas.121616198. Epub 2001 Jun 19.