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咖啡酸苯乙酯类似物对小鼠结肠26-L5癌细胞实验性肺转移的抑制作用。

Inhibitory effects of caffeic acid phenethyl ester analogues on experimental lung metastasis of murine colon 26-L5 carcinoma cells.

作者信息

Nagaoka Takema, Banskota Arjun H, Tezuka Yasuhiro, Harimaya Yuko, Koizumi Keiichi, Saiki Ikuo, Kadota Shigetoshi

机构信息

Institute of Natural Medicine, Toyama Medical and Pharmaceutical University, Sugitani, Japan.

出版信息

Biol Pharm Bull. 2003 May;26(5):638-41. doi: 10.1248/bpb.26.638.

Abstract

We have previously examined the antiproliferative activity of caffeic acid phenethyl ester (CAPE) and its 20 analogues against six tumor cell lines, and found that CAPE analogues possess selective antiproliferative activity toward the murine colon 26-L5 carcinoma cell line. To extend our study, the effects of CAPE analogues on the metastatic development of murine colon 26-L5 carcinoma cells in the lung were examined. The oral administration of CAPE (5 mg/mice/d) for 7 d after tumor inoculation decreased the tumor weight and the number of tumor nodules in the lung by 50% and 50%, respectively, compared to the control, while CAPE (5 mg/mice/d) administered for 7 d before tumor inoculation showed no significant effect. Besides CAPE, 4-phenylbutyl caffeate, 8-phenyl-7-octenyl caffeate, 2-cyclohexylethyl caffeate and n-octyl caffeate at an oral dose of 2 mg/mice/d caused a 55%, 43%, 55% and 35% reduction of the tumor nodules in their lung metastasis formation, respectively. These results further elaborate the possibility of CAPE and its analogues to become a new class of chemopreventive agents for the treatment of colon cancer metastasis.

摘要

我们之前研究了咖啡酸苯乙酯(CAPE)及其20种类似物对六种肿瘤细胞系的抗增殖活性,发现CAPE类似物对小鼠结肠26-L5癌细胞系具有选择性抗增殖活性。为了拓展我们的研究,我们检测了CAPE类似物对小鼠结肠26-L5癌细胞在肺部转移发展的影响。与对照组相比,在接种肿瘤后口服给予CAPE(5毫克/小鼠/天),持续7天,可使肿瘤重量和肺部肿瘤结节数量分别减少50%,而在接种肿瘤前给予CAPE(5毫克/小鼠/天),持续7天,则无显著效果。除了CAPE外,口服剂量为2毫克/小鼠/天的4-苯基丁基咖啡酸酯、8-苯基-7-辛烯基咖啡酸酯、2-环己基乙基咖啡酸酯和正辛基咖啡酸酯,在其肺转移形成过程中,分别使肿瘤结节减少了55%、43%、55%和35%。这些结果进一步阐明了CAPE及其类似物成为一类新型化学预防剂用于治疗结肠癌转移的可能性。

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