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从茜草中获得的一种新型抗肿瘤环六肽(RA-700)。

A novel antitumor cyclic hexapeptide (RA-700) obtained from Rubiae radix.

作者信息

Hamanaka T, Ohgoshi M, Kawahara K, Yamakawa K, Tsuruo T, Tsukagoshi S

机构信息

Ome Research Laboratories, Tobishi Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

J Pharmacobiodyn. 1987 Nov;10(11):616-23. doi: 10.1248/bpb1978.10.616.

DOI:10.1248/bpb1978.10.616
PMID:3128656
Abstract

The antitumor activity of a newly obtained cyclic hexapeptide, RA-700, from Rubiae Radix was studied using several murine experimental tumor systems. In P388 leukemia (inoculated intraperitoneally (i.p.), administered i.p.: i.p.-i.p.) the maximal increase in life span (ILSmax) resulting from an administration of RA-700 (4 mg/kg/d for 9 d) was 134% and the therapeutic ratio was 400. These values indicate that RA-700 has higher anti-tumor activity and broader active dose range than that of mitomycin C (MMC, 1 mg/kg/d for 9 d) which was used as a positive control. In the study of the treatment schedules on P388, RA-700 had the highest activity by consecutive injections. In MOPC-104E mouse plasmacytoma system (i.p.-i.p.), ILSmax of RA-700 (2.5 mg/kg/d for 9 d) was 84%. In a solid tumor, colon adenocarcinoma 38 (subcutaneously (s.c.)-intravenously (i.v.], RA-700 (4 mg/kg/d for 11 d) showed complete cures (8/8) compared to MMC (0.5 mg/kg/d for 11 d) which showed one cure out of 8 animals. In the study of a model of the inhibition of lymph node metastasis using P388 leukemia, the administration of RA-700 at more than 2.5 mg/kg/d i.v. for 7 d resulted in the survival of all animals (5/5) for over 60 d. In the amputation system of the same metastasis model at a dose of 4 mg/kg/d i.v. for 7 d, 3 animals out of 5 survived over 60 d.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用多种小鼠实验肿瘤模型,对从茜草中新获得的环六肽RA - 700的抗肿瘤活性进行了研究。在P388白血病模型(腹腔接种,腹腔给药:腹腔-腹腔)中,给予RA - 700(4mg/kg/d,共9天)后,最大寿命延长率(ILSmax)为134%,治疗指数为400。这些数值表明,RA - 700比用作阳性对照的丝裂霉素C(MMC,1mg/kg/d,共9天)具有更高的抗肿瘤活性和更宽的有效剂量范围。在P388治疗方案的研究中,连续注射时RA - 700活性最高。在MOPC - 104E小鼠浆细胞瘤模型(腹腔-腹腔)中,RA - 700(2.5mg/kg/d,共9天)的ILSmax为84%。在实体瘤结肠腺癌38模型(皮下-静脉)中,RA - 700(4mg/kg/d,共11天)使8只动物全部治愈(8/8),而MMC(0.5mg/kg/d,共11天)在8只动物中仅使1只治愈。在利用P388白血病模型抑制淋巴结转移的研究中,静脉注射RA - 700超过2.5mg/kg/d,持续7天,所有动物(5/5)存活超过60天。在同一转移模型的截肢系统中,静脉注射剂量为4mg/kg/d,持续7天,5只动物中有3只存活超过60天。(摘要截断于250字)

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