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吲哚醌EO9在人结肠腺癌模型中的细胞毒性评估。

Evaluation of the cytotoxicity of the indoloquinone eo9 in a human colon adenocarcinoma model.

作者信息

Bibby M, Cronin B, Phillips R

出版信息

Int J Oncol. 1993 Oct;3(4):661-6. doi: 10.3892/ijo.3.4.661.

Abstract

The development of anti-cancer drugs that are active in regions of low oxygen tension within solid tumours is an important goal for the chemotherapist. Equally as important is the utilization of appropriate model systems for their selection. This study describes morphological characteristics of multicellular spheroids derived from the human carcinoma cell line, DLD-1 and the evaluation of an investigational bioreductive alkylating agent (EO9) in monolayers, spheroids and xenografts. Histological examination of the cell line in vitro revealed typical features of glandular epithelium with microvilli on free surfaces and cell junction formation. Spheroids had acina formation, extensive necrosis and hypoxia at the time of treatment suggesting the spheroid model to be more representative of solid tumour geometry than more conventional in vitro test systems. EO9 is active against this cell line grown as a monolayer (IC50=0.76 mug ml-1) but is inactive against spheroids or established solid tumours in vivo. The suitability of this system for evaluating bioreductive drugs is discussed.

摘要

开发在实体瘤低氧张力区域具有活性的抗癌药物是化疗专家的一个重要目标。同样重要的是利用合适的模型系统来进行药物筛选。本研究描述了源自人癌细胞系DLD-1的多细胞球体的形态特征,并评估了一种研究性生物还原烷基化剂(EO9)在单层细胞、球体和异种移植模型中的效果。对该细胞系进行体外组织学检查,发现其具有腺上皮的典型特征,游离表面有微绒毛且形成了细胞连接。球体在治疗时出现腺泡形成、广泛坏死和缺氧,这表明球体模型比更传统的体外测试系统更能代表实体瘤的几何形状。EO9对单层培养的该细胞系有活性(IC50 = 0.76微克/毫升),但对球体或体内已形成的实体瘤无活性。本文讨论了该系统在评估生物还原药物方面的适用性。

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