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癌症化疗药物对作为原代组织培养生长的人类结直肠癌的活性。

Activity of cancer chemotherapeutic agents against human colorectal carcinomas grown as primary tissue culture.

作者信息

Zirvi K A, van der Bosch J, Masui H, Kaplan N O, Hill G J

出版信息

J Cancer Res Clin Oncol. 1987;113(1):20-6. doi: 10.1007/BF00389962.

Abstract

Improved procedures are described for the seeding of primary cultures from human colon adenocarcinoma and for the use of these cultures in the evaluation of drug effects. Two of the specimens studied were xenografts maintained in athymic (nude) mice, while the other six were biopsies obtained directly from patients. Tumor cells obtained directly from the patients proliferated in defined hormone-supplemented medium to the exclusion of other cells. In drug-response studies with cultures from a colon tumor biopsy all four drugs studied (4'-deoxydoxorubicin, 4'-O-methyldoxorubicin, 5-fluorouracil, and 1,3-bis-[chloroethyl]-1-nitrosourea) inhibited growth of the cells within 3-6 days after drug treatment. On an equitoxic dose basis (LD10 in mice), 4'-deoxydoxorubicin appeared to be the most active drug. This drug also showed dose-dependent activity against one of the xenografted tumors in vitro. In dose-response studies with cultures from another patient's colon tumor, doxorubicin and 5-fluorouracil showed significant activity against the tumor 10 days after the drug treatment with concentrations at 1X and 10X average peak plasma levels.

摘要

本文描述了改进的从人结肠腺癌中接种原代培养物以及使用这些培养物评估药物效果的方法。所研究的标本中有两个是在无胸腺(裸)小鼠中维持的异种移植瘤,另外六个是直接从患者身上获取的活检组织。直接从患者身上获得的肿瘤细胞在特定的添加激素的培养基中增殖,而其他细胞则被排除。在用来自结肠肿瘤活检组织的培养物进行的药物反应研究中,所研究的四种药物(4'-脱氧阿霉素、4'-O-甲基阿霉素、5-氟尿嘧啶和1,3-双[氯乙基]-1-亚硝基脲)在药物处理后3-6天内均抑制了细胞生长。在等毒性剂量基础上(小鼠的LD10),4'-脱氧阿霉素似乎是最具活性的药物。该药物在体外对其中一个异种移植瘤也显示出剂量依赖性活性。在用另一名患者结肠肿瘤的培养物进行的剂量反应研究中,阿霉素和5-氟尿嘧啶在以平均峰值血浆水平的1倍和10倍浓度进行药物处理10天后,对肿瘤显示出显著活性。

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