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从姬松茸中分离出的一种低分子量多糖可在体内抑制肿瘤生长和血管生成。

A low molecular weight polysaccharide isolated from Agaricus blazei suppresses tumor growth and angiogenesis in vivo.

作者信息

Niu Y C, Liu J C, Zhao X M, Wu X X

机构信息

Institute of Medicine, Qiqihar Medical College, Heilongjiang 161042, PR China.

出版信息

Oncol Rep. 2009 Jan;21(1):145-52.

Abstract

Previous studies indicated that the low molecular weight polysaccharide extracts from Agaricus blazei are potential antitumor agents or adjuvant in tumor treatment. In this study, we investigated the antitumor activity of LMPAB, a low molecular weight polysaccharide isolated from Agaricus blazei, and the molecular mechanisms of its antitumor activity. The antitumor effect of LMPAB was examined using mouse sarcoma 180 (S180) xenograft models. Antiangiogenic effect of LMPAB was determined by chicken embryo chorioallantoic membrane (CAM) angiogenesis and Matrigel-induced neovascularization in vivo models. The mRNA and protein levels of vascular endothelial growth factor (VEGF) were assessed using real-time reverse transcription-polymerase chain reaction, immunohistochemistry, and enzyme-linked immunosorbent assays. Tumor inhibitory rates in the S180 xenograft models were 9.7, 23.9, and 33.0%, respectively, after administration of LMPAB at dose of 50, 100, and 200 mg/kg/day for 2 weeks. LMPAB also inhibited angiogenesis in the CAM model and Matrigel-induced neovascularization in C57BL/6 mice. The mRNA and protein levels of VEGF in tumor tissues were significantly down-regulated in the BALB/c mice received LMPAB treatment. Furthermore, significant down-regulation of serum VEGF levels was also observed in the mice. Our data suggest that LMPAB might be a promising agent for tumor therapy, and the antitumor and antiangiogenic effects of LMPAB may be related with down-regulation of VEGF.

摘要

先前的研究表明,巴西蘑菇的低分子量多糖提取物是潜在的抗肿瘤药物或肿瘤治疗佐剂。在本研究中,我们研究了从巴西蘑菇中分离得到的低分子量多糖LMPAB的抗肿瘤活性及其抗肿瘤活性的分子机制。使用小鼠肉瘤180(S180)异种移植模型检测LMPAB的抗肿瘤作用。通过鸡胚绒毛尿囊膜(CAM)血管生成和基质胶诱导的体内新血管生成模型测定LMPAB的抗血管生成作用。使用实时逆转录-聚合酶链反应、免疫组织化学和酶联免疫吸附测定法评估血管内皮生长因子(VEGF)的mRNA和蛋白水平。在以50、100和200 mg/kg/天的剂量给予LMPAB 2周后,S180异种移植模型中的肿瘤抑制率分别为9.7%、23.9%和33.0%。LMPAB还抑制了CAM模型中的血管生成以及C57BL/6小鼠中基质胶诱导的新血管生成。在接受LMPAB治疗的BALB/c小鼠中,肿瘤组织中VEGF的mRNA和蛋白水平显著下调。此外,在小鼠中还观察到血清VEGF水平显著下调。我们的数据表明,LMPAB可能是一种有前途的肿瘤治疗药物,LMPAB的抗肿瘤和抗血管生成作用可能与VEGF的下调有关。

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