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血管生成抑制剂TNP - 470可抑制腹膜播散灶的生长。

Angiogenesis inhibitor, TNP-470, suppresses growth of peritoneal disseminating foci.

作者信息

Yoshikawa T, Yanoma S, Tsuburaya A, Kobayashi O, Sairenji M, Motohashi H, Noguchi Y

机构信息

Third Department of Surgery, Kanagawa Cancer Center, Yokohama, Japan.

出版信息

Hepatogastroenterology. 2000 Jan-Feb;47(31):298-302.

Abstract

BACKGROUND/AIMS: Angiogenesis is critical not only for growth of primary tumors but also for cells established at distant organs. We investigated the effects of angiogenesis inhibitor, TNP-470, on the establishment and growth of intraperitoneally inoculated human gastric cancer cell line, MKN-45, and survival of nude mice with this tumor.

METHODOLOGY

Human gastric cancer cell line, MKN-45, were injected into the peritoneal cavity of an ICR nude mouse and a model of peritoneal dissemination was developed. TNP-470 was injected subcutaneously every other day from day 1 until sacrifice or death. The effects of TNP-470 on MKN-45 cells were also examined in vitro.

RESULTS

Although the number of disseminated foci was not significantly different, the maximum size was significantly smaller in a TNP-treated group than those of a control. Survival time was significantly longer in a TNP-treated group. TNP-470 demonstrated no growth inhibition of MKN45 cells in vitro.

CONCLUSIONS

Those results suggested that anti-angiogenic agent, TNP-470, might be effective in treating peritoneal dissemination of gastric cancer by inhibiting growth of the seeded tumor cells on the peritoneum.

摘要

背景/目的:血管生成不仅对原发性肿瘤的生长至关重要,而且对远处器官定植的细胞也很关键。我们研究了血管生成抑制剂TNP - 470对腹腔内接种的人胃癌细胞系MKN - 45的定植和生长以及荷瘤裸鼠存活的影响。

方法

将人胃癌细胞系MKN - 45注入ICR裸鼠的腹腔,建立腹膜播散模型。从第1天开始每隔一天皮下注射TNP - 470,直至处死或死亡。还在体外检测了TNP - 470对MKN - 45细胞的影响。

结果

虽然播散灶的数量没有显著差异,但TNP治疗组的最大灶尺寸明显小于对照组。TNP治疗组的存活时间明显更长。TNP - 470在体外未显示对MKN45细胞有生长抑制作用。

结论

这些结果表明,抗血管生成剂TNP - 470可能通过抑制种植在腹膜上的肿瘤细胞生长而有效治疗胃癌腹膜播散。

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