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用于人膀胱移行细胞癌细胞的琼脂-甲基纤维素克隆形成试验的开发。

Development of an agar-methyl cellulose clonogenic assay for cells in transitional cell carcinoma of the human bladder.

作者信息

Buick R N, Stanisic T H, Fry S E, Salmon S E, Trent J M, Krasovich P

出版信息

Cancer Res. 1979 Dec;39(12):5051-6.

PMID:498131
Abstract

We report the development of a clonogenic assay for progenitor cells in transitional cell carcinoma of the bladder. Colony growth has been demonstrated from cells obtained both from surgical biopsies and from bladder barbotages. Electron microscopic and karyotypic evidence supports the contention that these progenitors represent a part of the population maintaining the tumor in vivo. Colony growth occurred in 9 of 11 surgical biopsy samples and in 6 of 6 bladder barbotage samples. Plating efficiency ranged up to 0.7%, and colony size was in some instances greater than 1000 cells. The assay appears potentially useful for analysis of the biology of human transitional cell carcinoma.

摘要

我们报告了一种用于膀胱移行细胞癌祖细胞的克隆形成试验的开发。已证明从手术活检和膀胱灌洗获得的细胞能够形成集落。电子显微镜和核型证据支持这些祖细胞代表体内维持肿瘤的一部分细胞群体这一论点。11个手术活检样本中有9个出现集落生长,6个膀胱灌洗样本中有6个出现集落生长。接种效率高达0.7%,在某些情况下集落大小超过1000个细胞。该试验对于分析人类移行细胞癌的生物学特性可能具有潜在用途。

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