首页> 外文OA文献 >Intensification therapy with anti-parathyroid hormone-related protein antibody plus zoledronic acid for bone metastases of small cell lung cancer cells in severe combined immunodeficient mice
【2h】

Intensification therapy with anti-parathyroid hormone-related protein antibody plus zoledronic acid for bone metastases of small cell lung cancer cells in severe combined immunodeficient mice

机译:抗甲状旁腺激素相关蛋白抗体加唑来膦酸强化治疗重症联合免疫缺陷小鼠小细胞肺癌细胞骨转移

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Bone metastases occur in more than one-third of patients with advanced lung cancer and are difficult to treat. We showed previously the therapeutic effect of a third-generation bisphosphonate, minodronate, and antiparathyroid hormone-related protein (PTHrP) neutralizing antibody on bone metastases induced by the human small cell lung cancer cell line, SBC-5, in natural killer cell-depleted severe combined immunodeficient mice. The purpose of our current study was to examine the effect of the combination of PTHrP antibody and zoledronic acid, which has been approved to treat bone metastases, against bone metastases produced by SBC-5 cells expressing PTHrP. Treatment with PTHrP antibody and/or zoledronic acid did not affect the proliferation of SBC-5 cells in vitro. Repeated treatments with either PTHrP antibody or zoledronic acid inhibited the formation of osteolytic bone metastases of SBC-5 cells but had no effect on metastases to visceral organs. Importantly, combined treatment with PTHrP antibody and zoledronic acid further inhibited the formation of bone metastases. Histologic assays showed that, compared with either PTHrP antibody or zoledronic acid alone, their combination decreased the number of tumor-associated osteoclasts and increased the number of apoptotic tumor cells. These findings suggest that this novel dual-targeting therapy may be useful for controlling bone metastases in a subpopulation of small cell lung cancer patients. Copyright © 2009 American Association for Cancer Research.全文公開201001
机译:超过三分之一的晚期肺癌患者会发生骨转移,并且难以治疗。我们先前显示了第三代双膦酸盐,米诺膦酸盐和抗甲状旁腺激素相关蛋白(PTHrP)中和抗体对人小细胞肺癌细胞系SBC-5在自然杀伤细胞耗竭后所诱发的骨转移的治疗作用严重的联合免疫缺陷小鼠。我们当前研究的目的是检验PTHrP抗体和唑来膦酸的组合(已被批准用于治疗骨转移)对表达PTHrP的SBC-5细胞产生的骨转移的作用。用PTHrP抗体和/或唑来膦酸处理不会影响SBC-5细胞的体外增殖。用PTHrP抗体或唑来膦酸重复治疗可抑制SBC-5细胞溶骨性骨转移的形成,但对内脏器官的转移没有影响。重要的是,PTHrP抗体和唑来膦酸的联合治疗进一步抑制了骨转移瘤的形成。组织学分析表明,与单独的PTHrP抗体或唑来膦酸相比,它们的组合减少了肿瘤相关破骨细胞的数量,并增加了凋亡性肿瘤细胞的数量。这些发现表明,这种新颖的双重靶向疗法可能对控制小细胞肺癌患者亚群中的骨转移有用。版权所有©2009美国癌症研究协会。全文公开201001

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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