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Vaticanol C,一种新型白藜芦醇四聚体,可减少携带p53突变的小鼠乳腺癌的淋巴结转移和肺转移。

Vaticanol C, a novel resveratrol tetramer, reduces lymph node and lung metastases of mouse mammary carcinoma carrying p53 mutation.

作者信息

Shibata Masa-Aki, Akao Yukihiro, Shibata Eiko, Nozawa Yoshinori, Ito Tetsuro, Mishima Satoshi, Morimoto Junji, Otsuki Yoshinori

机构信息

Department of Anatomy and Cell Biology, Division of Basic Medicine I, Osaka Medical College, 2-7, Daigaku-machi, Takatsuki, Japan.

出版信息

Cancer Chemother Pharmacol. 2007 Oct;60(5):681-91. doi: 10.1007/s00280-007-0414-y. Epub 2007 Jan 26.

Abstract

PURPOSE

The effects of vaticanol C (Vat-C), a novel resveratrol tetramer, were studied in a mouse metastatic mammary cancer model carrying mutations in p53 that produce a metastatic spectrum similar to that seen in human breast cancers.

METHODS

Mammary tumors, induced by inoculation of syngeneic BALB/c mice with BJMC3879 cells, were subsequently treated with Vat-C at 0, 100 and 200 ppm in their diet.

RESULTS

The in vitro study demonstrated that Vat-C induced apoptosis, as inferred by morphological changes, nucleosomal DNA fragmentation and elevated activities of caspases. Although tumor volumes were not apparently suppressed in mice treated with Vat-C, the multiplicity of lymph node metastasis was significantly decreased in the 200-ppm group. Furthermore, the multiplicity of lung metastasis was also significantly lower in the 200-ppm group. In any category of organ metastasis, the number of organs with metastasis tended to be lower in the 200-ppm group, but these findings were not statistically significant. The levels of apoptosis were significantly higher in the 200-ppm group, but DNA synthesis only a tended to be lower in this group. Microvessel density in tumors also tended to be lower in the Vat-C-treated groups. Moreover, the numbers of lymphatic vessels having intraluminal tumor cells was significantly lower in mammary tumors of mice given 100 and 200-ppm Vat-C, indicating a reduction in migrating tumor cells into the lymphatic vessels of tumor tissue.

CONCLUSIONS

These results suggest that the observed antimetastatic activity of Vat-C may be of clinical significance as an adjuvant therapy in metastatic human breast cancer having p53 mutations, and may also be useful as a chemopreventative of breast cancer development.

摘要

目的

在携带p53突变的小鼠转移性乳腺癌模型中研究新型白藜芦醇四聚体vaticanol C(Vat-C)的作用,该模型产生的转移谱与人类乳腺癌相似。

方法

通过将同基因BALB/c小鼠接种BJMC3879细胞诱导乳腺肿瘤,随后在其饮食中分别添加0、100和200 ppm的Vat-C进行处理。

结果

体外研究表明,Vat-C可诱导细胞凋亡,这可通过形态学变化、核小体DNA片段化和半胱天冬酶活性升高来推断。虽然用Vat-C处理的小鼠肿瘤体积未明显受到抑制,但200 ppm组的淋巴结转移多样性显著降低。此外,200 ppm组的肺转移多样性也显著降低。在任何器官转移类别中,200 ppm组有转移的器官数量往往较少,但这些结果无统计学意义。200 ppm组的细胞凋亡水平显著更高,但该组的DNA合成仅呈下降趋势。Vat-C处理组肿瘤中的微血管密度也往往较低。此外,给予100和200 ppm Vat-C的小鼠乳腺肿瘤中,腔内有肿瘤细胞的淋巴管数量显著减少,表明迁移到肿瘤组织淋巴管中的肿瘤细胞减少。

结论

这些结果表明,观察到的Vat-C的抗转移活性作为p53突变的转移性人类乳腺癌辅助治疗可能具有临床意义,也可能作为乳腺癌发展的化学预防剂。

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