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摄入葡萄来源的多酚通过抑制血管生成和诱导细胞凋亡来减少 C26 肿瘤的生长。

Intake of grape-derived polyphenols reduces C26 tumor growth by inhibiting angiogenesis and inducing apoptosis.

机构信息

UMR 7213 CNRS, Laboratoire de Biophotonique et de Pharmacologie, Faculté de Pharmacie, Université de Strasbourg, 74 route du Rhin, 67401 Illkirch, France.

出版信息

FASEB J. 2010 Sep;24(9):3360-9. doi: 10.1096/fj.09-149419. Epub 2010 May 4.

Abstract

This study evaluated the in vivo antitumor activity of grape-derived polyphenols. BALB/c mice were subcutaneously implanted with C26 colon carcinoma cells, and 2 d later they received either solvent or red wine polyphenols (RWPs) (100 mg/kg/d, human equivalent dose approximately 500 mg/d) in the drinking water for 25 d. Wistar rats received either solvent or RWPs (100 mg/kg/d, human equivalent dose approximately 1000 mg/d) in the drinking water 1 wk before injection of azoxymethane and were studied 10 wk later. In mice, RWPs inhibited tumor growth by 31%, reduced tumor vascularization and the number of lung metastases, decreased proliferation as indicated by down-regulation of Ki67, cyclin D1, and UHRF1, and increased apoptosis as indicated by TUNEL staining and active caspase-3 levels in tumor cells. RWPs reduced expression of VEGF, matrix metalloproteinase (MMP)-2, MMP-9, and cyclooxygenase-2 and increased expression of tumor suppressor genes p16(INK4A), p53, and p73 in tumor cells. In rats, RWPs reduced by 49% the number of azoxymethane-induced aberrant crypt foci (preneoplastic lesions) in colon. Thus, RWPs effectively reduced the development of colon carcinoma tumors in vivo by blunting tumor vascularization and by inhibiting proliferation and promoting apoptosis of tumor cells subsequent to an up-regulation of tumor suppressor genes.

摘要

本研究评估了葡萄来源的多酚在体内的抗肿瘤活性。BALB/c 小鼠皮下植入 C26 结肠癌细胞,2 天后,它们通过饮用水分别接受溶剂或红葡萄酒多酚(RWPs)(100mg/kg/d,人类等效剂量约为 500mg/d),共 25 天。Wistar 大鼠在注射氧化偶氮甲烷前 1 周通过饮用水分别接受溶剂或 RWPs(100mg/kg/d,人类等效剂量约为 1000mg/d),并在 10 周后进行研究。在小鼠中,RWPs 抑制肿瘤生长 31%,减少肿瘤血管生成和肺转移数量,下调 Ki67、cyclin D1 和 UHRF1 表明增殖减少,并通过 TUNEL 染色和肿瘤细胞中活性 caspase-3 水平表明凋亡增加。RWPs 降低了肿瘤细胞中 VEGF、基质金属蛋白酶(MMP)-2、MMP-9 和环氧化酶-2 的表达,并增加了肿瘤抑制基因 p16(INK4A)、p53 和 p73 的表达。在大鼠中,RWPs 使氧化偶氮甲烷诱导的结肠异常隐窝病灶(癌前病变)数量减少了 49%。因此,RWPs 通过抑制肿瘤血管生成以及通过上调肿瘤抑制基因抑制肿瘤细胞增殖和促进凋亡,有效减少了体内结肠癌肿瘤的发展。

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