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OK432抑制F344大鼠结肠腺癌ACL-15的实验性肝转移。

OK432 inhibits experimental hepatic metastasis of colon adenocarcinoma ACL-15 in F344 rats.

作者信息

Sugimoto F, Tsukada K, Hatakeyama K, Yoshida K, Muto T

机构信息

First Department of Surgery, Niigata University School of Medicine, Japan.

出版信息

Surg Today. 1994;24(8):694-700. doi: 10.1007/BF01636774.

Abstract

The effect of OK432 on hepatic metastasis, induced by inoculating 1 x 10(6) ACL-15 cells from a rat colon adenocarcinoma cell line into the ileocolic vein of male F344 rats, was investigated in this study. Metastases were detected 14 days after inoculation in the control rats, however, pretreatment 3 days prior to the tumor cell inoculation with an anti-asialoGM1 antibody, which eliminates natural killer (NK) cell activity in vitro, increased the number of hepatic metastases, shortened the survival time, and decreased the NK activity of the nonparenchymal liver cells (NPC). In contrast, pretreatment with OK432 2 days prior to tumor inoculation significantly decreased the number of hepatic metastases, prolonged the survival time, and augmented the NK activity of the NPC, although treatment with OK432 3 or 7 days after inoculation did not decrease the number of hepatic metastases. Moreover, NPC from the OK432-pretreated rats had a marked antitumor effect against ACL-15 cells in the Winn's neutralization test. The results of this study indicate that pretreatment with OK432 before tumor cell inoculation inhibits hepatic metastasis in this experimental model, possibly by augmentating liver-associated NK activity.

摘要

本研究探讨了OK432对肝转移的影响,具体方法是将1×10(6)个来自大鼠结肠腺癌细胞系的ACL-15细胞接种到雄性F344大鼠的回结肠静脉中诱导肝转移。接种后14天在对照大鼠中检测到转移灶,然而,在肿瘤细胞接种前3天用抗去唾液酸GM1抗体进行预处理,该抗体在体外消除自然杀伤(NK)细胞活性,结果增加了肝转移灶数量,缩短了生存时间,并降低了非实质肝细胞(NPC)的NK活性。相比之下,在肿瘤接种前2天用OK432进行预处理显著减少了肝转移灶数量,延长了生存时间,并增强了NPC的NK活性,尽管接种后3天或7天用OK432治疗并没有减少肝转移灶数量。此外,在Winn中和试验中,来自OK432预处理大鼠的NPC对ACL-15细胞具有显著的抗肿瘤作用。本研究结果表明,在肿瘤细胞接种前用OK432进行预处理可抑制该实验模型中的肝转移,可能是通过增强肝脏相关的NK活性实现的。

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