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HO-221与多种抗肿瘤药物联合对L 1210白血病的作用

[Combined effect of HO-221 with various antitumor agents against L 1210 leukemia].

作者信息

Nakajima T, Masuda H, Okamoto T, Watanabe M, Yokoyama K, Yamada N, Tsukagoshi S, Taguchi T

机构信息

Research Division, Green Cross Corporation.

出版信息

Gan To Kagaku Ryoho. 1991 Apr;18(4):555-62.

PMID:2012397
Abstract

Combined effect of N-[4-(5-bromo-2-pyrimidinyloxy)-3-chlorophenyl]-N'-(2-nitrobenzoyl ) urea, HO-221, with various antitumor agents was studied using L 1210 leukemia in vivo and in vitro. Ten anticancer drugs were chosen from alkylating agents, antitumor antibiotics, antimetabolites and plant alkaloids each. The combined effect was assessed by comparing ILS (increase of life span) in the combined group with the sum of ILS of each single agent. Synergistic effect was considered to exist if ILS of the combination-treatment group exceeds the sum of those in 2 single-treatment groups. The two-drug combination of HO-221 with cyclophosphamide (CPA), adriamycin (ADM), mitomycin C (MMC), vindesine (VDS), vincristine (VCR) or etoposide showed remarkable synergistic effects with 60-days survivors. However, the combination chemotherapy with antimetabolites, 5-fluorouracil (5-FU) and methotrexate (MTX) showed competitive effects. Moreover, the synergistic cytocidal effect in vitro by the clonogenic assay was observed in combination of HO-221 with the same drug using in vivo test. The present results indicate that HO-221 seems to be a useful antitumor agent in combination chemotherapy.

摘要

利用L 1210白血病在体内和体外研究了N-[4-(5-溴-2-嘧啶氧基)-3-氯苯基]-N'-(2-硝基苯甲酰基)脲(HO-221)与各种抗肿瘤药物的联合效应。从烷基化剂、抗肿瘤抗生素、抗代谢物和植物生物碱中各选取了10种抗癌药物。通过比较联合组的生命延长率(ILS)与每种单一药物的ILS之和来评估联合效应。如果联合治疗组的ILS超过两个单一治疗组的ILS之和,则认为存在协同效应。HO-221与环磷酰胺(CPA)、阿霉素(ADM)、丝裂霉素C(MMC)、长春地辛(VDS)、长春新碱(VCR)或依托泊苷的两药联合对60天存活者显示出显著的协同效应。然而,与抗代谢物5-氟尿嘧啶(5-FU)和甲氨蝶呤(MTX)的联合化疗显示出竞争效应。此外,在体外克隆形成试验中观察到HO-221与体内试验中使用的相同药物联合具有协同杀细胞效应。目前的结果表明,HO-221在联合化疗中似乎是一种有用的抗肿瘤药物。

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Antitumor activity on murine tumors of a novel antitumor benzoylphenylurea derivative, HO-221.
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