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一种新型人膀胱癌细胞系UCRU-BL-28的特性分析。

Characterization of a new human bladder cancer cell line, UCRU-BL-28.

作者信息

Russell P J, Palavidis Z, Rozinova E, Philips J, Wills E J, Lukeis R, Wass J, Raghavan D

机构信息

Kanematsu Laboratory, Royal Prince Alfred Hospital, New South Wales, Australia.

出版信息

J Urol. 1993 Sep;150(3):1038-44. doi: 10.1016/s0022-5347(17)35682-3.

DOI:10.1016/s0022-5347(17)35682-3
PMID:8345582
Abstract

A new human bladder cancer cell line, UCRU-BL-28 has been established and characterized from a relapsed, cisplatin resistant, grade II, stage T4 tumor. This line is tumorigenic in nude mice and reflects the pathology of the original tumor. The morphology, the expression of tumor-associated antigens and EGF receptors, and the ability to grow both in an anchorage independent manner and in the absence of serum is explored. The BL-28 line has 71-74XXY chromosomes, with del 5q, der(9) and i(19q). Further studies on the molecular basis of bladder cancer, chemosensitivity to cisplatin, growth factor production and tissue invasion are under way.

摘要

一种新的人膀胱癌细胞系UCRU-BL-28已从一例复发的、顺铂耐药的II级、T4期肿瘤中建立并进行了特征描述。该细胞系在裸鼠中具有致瘤性,并反映了原发肿瘤的病理学特征。对其形态、肿瘤相关抗原和表皮生长因子受体的表达以及在非锚定依赖方式和无血清条件下生长的能力进行了研究。BL-28细胞系具有71 - 74XXY染色体,伴有5号染色体长臂缺失、9号衍生染色体和19号染色体等臂染色体。关于膀胱癌分子基础、对顺铂的化学敏感性、生长因子产生和组织侵袭的进一步研究正在进行中。

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Characterization of a new human bladder cancer cell line, UCRU-BL-28.一种新型人膀胱癌细胞系UCRU-BL-28的特性分析。
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引用本文的文献

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Methylation of a CpG island within the uroplakin Ib promoter: a possible mechanism for loss of uroplakin Ib expression in bladder carcinoma.尿路上皮蛋白Ib启动子内CpG岛的甲基化:膀胱癌中尿路上皮蛋白Ib表达缺失的一种可能机制。
Neoplasia. 2004 Mar-Apr;6(2):128-35. doi: 10.1593/neo.03337.
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Isolation and characterization of a novel bladder cancer cell line: inhibition by epidermal growth factor.一种新型膀胱癌细胞系的分离与鉴定:受表皮生长因子抑制
In Vitro Cell Dev Biol Anim. 1998 Oct;34(9):722-8. doi: 10.1007/s11626-998-0068-z.
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Antiproliferative effects of bacillus Calmette-Guerin and interferon alpha 2b on human bladder cancer cells in vitro.
卡介苗和干扰素α2b对人膀胱癌细胞的体外抗增殖作用。
Cancer Immunol Immunother. 1995 Nov;41(5):309-16. doi: 10.1007/BF01517219.