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人膀胱癌细胞系MGH-U1的单层细胞和球体对膀胱内化疗所用药物的敏感性。

Sensitivities of monolayers and spheroids of the human bladder cancer cell line MGH-U1 to the drugs used for intravesical chemotherapy.

作者信息

Knuchel R, Hofstadter F, Jenkins W E, Masters J R

机构信息

Department of Pathology, RWTH, Aachen, West Germany.

出版信息

Cancer Res. 1989 Mar 15;49(6):1397-401.

PMID:2493980
Abstract

The in vitro cytotoxicities of the four drugs most frequently used for intravesical chemotherapy (Adriamycin, epodyl, mitomycin C, Thiotepa) and epirubicin were compared using monolayers and multicellular tumor spheroids of the human bladder cancer cell line, MGH-U1. Adriamycin and epirubicin were most cytotoxic against monolayer cultures, whereas mitomycin C killed more cells in spheroids. Epodyl was least cytotoxic against both two- and three-dimensional cultures. Thiotepa was the only drug more cytotoxic to three- than two-dimensional cultures. Topographic analysis of bromodeoxyuridine-stained nuclei using image analysis indicated that Adriamycin selectively removed or killed superficial cells in multicellular tumor spheroids, but had little effect on DNA synthesis within the spheroids. In contrast Thiotepa killed cells throughout the spheroids. These in vitro data appear to reflect clinical experience using intravesical chemotherapy to treat superficial bladder cancer.

摘要

使用人膀胱癌细胞系MGH-U1的单层细胞和多细胞肿瘤球体,比较了膀胱内化疗最常用的四种药物(阿霉素、表柔比星、丝裂霉素C、噻替派)和表阿霉素的体外细胞毒性。阿霉素和表阿霉素对单层培养细胞的细胞毒性最大,而丝裂霉素C在球体中杀死的细胞更多。表柔比星对二维和三维培养细胞的细胞毒性最小。噻替派是唯一一种对三维培养细胞的细胞毒性大于二维培养细胞的药物。使用图像分析对溴脱氧尿苷染色的细胞核进行拓扑分析表明,阿霉素选择性地去除或杀死了多细胞肿瘤球体中的表层细胞,但对球体内的DNA合成影响很小。相比之下,噻替派杀死了整个球体中的细胞。这些体外数据似乎反映了使用膀胱内化疗治疗浅表性膀胱癌的临床经验。

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