首页> 外文期刊>Cancer biology & therapy >Acidic mucopolysaccharide from Holothuria leucospilota has antitumor effect by inhibiting angiogenesis and tumor cell invasion in vivo and in vitro.
【24h】

Acidic mucopolysaccharide from Holothuria leucospilota has antitumor effect by inhibiting angiogenesis and tumor cell invasion in vivo and in vitro.

机译:来自白斑霍霍氏菌的酸性粘多糖通过在体内和体外抑制血管生成和肿瘤细胞侵袭而具有抗肿瘤作用。

获取原文
获取原文并翻译 | 示例
           

摘要

Acidic mucopolysaccharide from Holothuria Leucospilota (HS) may affect some steps in metastasis cascade. In vitro, HS inhibited the growth of B16F10 cells and proliferation of VEGF-induced HUVEC dose-dependently compared to the control, VEGF-induced capillary-like tube networks and the numbers of migratory and invasive cells were significantly inhibited by HS in a dose-dependent manner under the cytotoxic doses. Additionally, VEGF-induced vessel sprouting of rat aortic ring was also inhibited by HS. It also has been demonstrated that the invasive ability of B16F10 melanoma cells through the Matrigel-embedded Boyden chamber was suppressed by 0.5 muM HS. The protein level secreted by B16F10 cells of MMP-2,-9 and VEGF were decreased by HS treatment. In vivo, a tumor growth inhibition study was carried out using mice bearing B16F10 cells model of metastasis, no matter experimental or spontaneous, showed that HS at 5.2, 11.6 and 26 mg/kg (weight of mice) could markedly decreased the metastatic tumors in mouse lung in a dose-dependent manner. In CAM assay and Matrigel plug assay in vivo, HS (50 microg/egg and 100 microg/egg) inhibited new blood vessel formation on the growing chick chorioallantoic membrane, and HS (5.2 and 26 mg/kg body weight) reduced the vessel density in Matrigel plugs implanted in mice. Taken together, these results demonstrate that HS has antimetastasic properties possibly via its antiangiogenesis induced by downregulation of VEGF and suppression of invasive ability of cancer cells mediated by downregulation of MMP-2, -9 and their activities.
机译:嗜盐壶菌(HS)的酸性粘多糖可能会影响转移级联反应的某些步骤。与对照,VEGF诱导的毛细血管样管网络相比,HS在体外抑制B16F10细胞的生长和VEGF诱导的HUVEC的增殖具有剂量依赖性,并且HS显着抑制了迁移和侵袭细胞的数量。依赖方式下的细胞毒剂量。此外,HS还可抑制VEGF诱导的大鼠主动脉环血管萌芽。还已经证明,通过0.5μMHS抑制了B16F10黑素瘤细胞通过嵌入基质胶的Boyden室的侵袭能力。 HS处理可降低MMP-2,-9和VEGF的B16F10细胞分泌的蛋白水平。在体内,使用带有转移模型的B16F10细胞的小鼠进行了肿瘤生长抑制研究,无论是实验的还是自发的,均表明5.2、11.6和26 mg / kg(小鼠体重)的HS可以显着降低小鼠体内的转移性肿瘤。小鼠肺部呈剂量依赖性。在体内的CAM分析和Matrigel堵塞分析中,HS(50微克/蛋和100微克/蛋)抑制生长中的鸡尿囊尿膜上新血管的形成,而HS(5.2和26 mg / kg体重)降低血管密度植入小鼠体内的Matrigel塞中。综上所述,这些结果表明HS可能具有抗转移特性,这可能是由于VEGF的下调引起的抗血管生成和MMP-2,-9及其活性下调所介导的癌细胞侵袭能力的抑制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号