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多胺生物合成抑制剂DL-α-二氟甲基鸟氨酸在小鼠体内的抗转移活性

Antimetastatic activity of DL-alpha-difluoromethylornithine, an inhibitor of polyamine biosynthesis, in mice.

作者信息

Sunkara P S, Rosenberger A L

出版信息

Cancer Res. 1987 Feb 15;47(4):933-5.

PMID:3100031
Abstract

Our earlier studies indicated a role for polyamines (namely, putrescine, spermidine, and spermine) not only in tumor growth but also in tumor metastases. We have observed that administration of alpha-difluoromethylornithine (DFMO), an irreversible inhibitor of ornithine decarboxylase, resulted in significant inhibition of visually detectable pulmonary metastases in mice implanted with Lewis lung carcinoma. The objective of the present study is to investigate the effect of DFMO on other spontaneous and experimental metastatic models and also to determine which step(s) in the tumor metastatic cascade is sensitive to DFMO. The results presented in this study with malignant mouse B16 amelanotic melanoma (B16a) showed a dose-dependent effect of DFMO on the inhibition of both tumor growth and grossly detectable pulmonary metastases. DFMO, when administered as 0.5, 1, and 2% solution in drinking water, resulted in 0, 24.5, and 60% inhibition of tumor growth, respectively, whereas at the same doses an inhibition of 55, 83, and 96% of visible metastases was observed. At treatment levels of 1 and 2% DFMO, 30 and 65% of the animals were free of metastases. DFMO, at 0.5%, did not show any effect on tumor growth, while a significant 55% inhibition of visible pulmonary metastasis was observed, suggesting a specific role for polyamines in tumor metastasis. DFMO treatment also resulted in a significant reduction of putrescine and spermidine levels with a slight increase in spermine concentration in the tumor tissue. DFMO administration did not inhibit the experimental metastases induced as a result of i.v. injection of B16 melanoma (line F10) tumor and Lewis lung carcinoma cells into the tail vein. These results provide preliminary evidence to indicate that tumor cell polyamine depletion by DFMO might affect the first step in the metastatic cascade, intravasation (i.e., prevent the invasion of metastatic tumor cells into lymphatics or blood vessels), although the effect of DFMO on other steps in the metastatic cascade cannot be ruled out.

摘要

我们早期的研究表明,多胺(即腐胺、亚精胺和精胺)不仅在肿瘤生长中起作用,还在肿瘤转移中发挥作用。我们观察到,给予鸟氨酸脱羧酶的不可逆抑制剂α-二氟甲基鸟氨酸(DFMO),可显著抑制接种Lewis肺癌的小鼠中肉眼可见的肺转移。本研究的目的是研究DFMO对其他自发和实验性转移模型的影响,并确定肿瘤转移级联反应中的哪一步对DFMO敏感。本研究中关于恶性小鼠B16无黑色素黑色素瘤(B16a)的结果显示,DFMO对肿瘤生长和肉眼可见的肺转移抑制具有剂量依赖性效应。当以0.5%、1%和2%的溶液形式给予饮用水中的DFMO时,分别导致肿瘤生长抑制率为0%、24.5%和60%,而在相同剂量下,观察到可见转移的抑制率分别为55%、83%和96%。在1%和2%的DFMO治疗水平下,分别有30%和65%的动物没有转移。0.5%的DFMO对肿瘤生长没有任何影响,而观察到可见肺转移有显著的55%的抑制率,这表明多胺在肿瘤转移中具有特定作用。DFMO治疗还导致肿瘤组织中腐胺和亚精胺水平显著降低,而精胺浓度略有增加。给予DFMO并未抑制通过将B16黑色素瘤(F10系)肿瘤和Lewis肺癌细胞静脉注射到尾静脉所诱导的实验性转移。这些结果提供了初步证据,表明DFMO使肿瘤细胞多胺耗竭可能会影响转移级联反应的第一步,即血管内侵入(即防止转移性肿瘤细胞侵入淋巴管或血管),尽管不能排除DFMO对转移级联反应中其他步骤的影响。

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